[
  {
    "id": "C0002736",
    "id2": "MedGen UID:274",
    "medgen_label": "Amyotrophic lateral sclerosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/274",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0004976",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004976",
    "nando_id": "NANDO:1200002"
  },
  {
    "id": "C0007222",
    "id2": "MedGen UID:2848",
    "medgen_label": "Disorder of cardiovascular system",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/2848",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0004995",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004995",
    "nando_id": "NANDO:1100005"
  },
  {
    "id": "C0007758",
    "id2": "MedGen UID:849",
    "medgen_label": "Cerebellar ataxia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/849",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000437",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000437",
    "nando_id": "NANDO:1200037"
  },
  {
    "id": "C0023521",
    "id2": "MedGen UID:44131",
    "medgen_label": "Galactosylceramide beta-galactosidase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44131",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009499",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009499",
    "nando_id": "NANDO:1200074"
  },
  {
    "id": "C0024408",
    "id2": "MedGen UID:9841",
    "medgen_label": "Azorean disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9841",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007182",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007182",
    "nando_id": "NANDO:1200041"
  },
  {
    "id": "C0025517",
    "id2": "MedGen UID:44376",
    "medgen_label": "Metabolic disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44376",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005066",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005066",
    "nando_id": "NANDO:1100002"
  },
  {
    "id": "C0026769",
    "id2": "MedGen UID:10123",
    "medgen_label": "Multiple sclerosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10123",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005301",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005301",
    "nando_id": "NANDO:1200023"
  },
  {
    "id": "C0026847",
    "id2": "MedGen UID:7755",
    "medgen_label": "Spinal muscular atrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7755",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001516",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001516",
    "nando_id": "NANDO:1200003"
  },
  {
    "id": "C0030567",
    "id2": "MedGen UID:10590",
    "medgen_label": "Parkinson disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10590",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005180",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005180",
    "nando_id": "NANDO:1200010"
  },
  {
    "id": "C0268250",
    "id2": "MedGen UID:78652",
    "medgen_label": "Gaucher disease type II",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78652",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009266",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009266",
    "nando_id": "NANDO:1200058"
  },
  {
    "id": "C0268251",
    "id2": "MedGen UID:78653",
    "medgen_label": "Gaucher disease type III",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78653",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009267",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009267",
    "nando_id": "NANDO:1200059"
  },
  {
    "id": "C0268271",
    "id2": "MedGen UID:75665",
    "medgen_label": "Infantile GM1 gangliosidosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75665",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009260",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009260",
    "nando_id": "NANDO:1200067"
  },
  {
    "id": "C0268272",
    "id2": "MedGen UID:120625",
    "medgen_label": "GM1 gangliosidosis type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120625",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009261",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009261",
    "nando_id": "NANDO:1200068"
  },
  {
    "id": "C0268273",
    "id2": "MedGen UID:78655",
    "medgen_label": "GM1 gangliosidosis type 3",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78655",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009262",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009262",
    "nando_id": "NANDO:1200069"
  },
  {
    "id": "C0393571",
    "id2": "MedGen UID:98276",
    "medgen_label": "Multiple system atrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/98276",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007803",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007803",
    "nando_id": "NANDO:1200034"
  },
  {
    "id": "C0393576",
    "id2": "MedGen UID:98277",
    "medgen_label": "Chorea-acanthocytosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/98277",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008695",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008695",
    "nando_id": "NANDO:1200014"
  },
  {
    "id": "C0393819",
    "id2": "MedGen UID:98292",
    "medgen_label": "Chronic inflammatory demyelinating polyradiculoneuropathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/98292",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006702",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006702",
    "nando_id": "NANDO:1200030"
  },
  {
    "id": "C1859598",
    "id2": "MedGen UID:395301",
    "medgen_label": "Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/395301",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008842",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008842",
    "nando_id": "NANDO:1200051"
  },
  {
    "id": "C1861736",
    "id2": "MedGen UID:348439",
    "medgen_label": "Spinocerebellar ataxia type 31",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/348439",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007296",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007296",
    "nando_id": "NANDO:1200044"
  },
  {
    "id": "C4083008",
    "id2": "MedGen UID:901636",
    "medgen_label": "Guillain-Barre syndrome, familial",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/901636",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0007691",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007691",
    "nando_id": "NANDO:1200030"
  },
  {
    "id": "C0085078",
    "id2": "MedGen UID:43098",
    "medgen_label": "Lysosomal storage disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/43098",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002561",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002561",
    "nando_id": "NANDO:1200055"
  },
  {
    "id": "C0035204",
    "id2": "MedGen UID:48421",
    "medgen_label": "Respiratory system disorder",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/48421",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005087",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005087",
    "nando_id": "NANDO:1100010"
  },
  {
    "id": "C1961835",
    "id2": "MedGen UID:409531",
    "medgen_label": "Gaucher disease type I",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/409531",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009265",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009265",
    "nando_id": "NANDO:1200057"
  },
  {
    "id": "C0014130",
    "id2": "MedGen UID:4043",
    "medgen_label": "Disorder of endocrine system",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/4043",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005151",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005151",
    "nando_id": "NANDO:1100009"
  },
  {
    "id": "C0018939",
    "id2": "MedGen UID:5483",
    "medgen_label": "Hematologic disorder",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5483",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005570",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005570",
    "nando_id": "NANDO:1100006"
  },
  {
    "id": "C0020179",
    "id2": "MedGen UID:5654",
    "medgen_label": "Huntington disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5654",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007739",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007739",
    "nando_id": "NANDO:1200012"
  },
  {
    "id": "C0021053",
    "id2": "MedGen UID:5759",
    "medgen_label": "Immune system disorder",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5759",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005046",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005046",
    "nando_id": "NANDO:1100004"
  },
  {
    "id": "C0238190",
    "id2": "MedGen UID:68659",
    "medgen_label": "Inclusion body myositis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/68659",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007827",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007827",
    "nando_id": "NANDO:1200032"
  },
  {
    "id": "C0751781",
    "id2": "MedGen UID:155630",
    "medgen_label": "Dentatorubral-pallidoluysian atrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155630",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007435",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007435",
    "nando_id": "NANDO:1200043"
  },
  {
    "id": "C0751964",
    "id2": "MedGen UID:155968",
    "medgen_label": "Primary progressive multiple sclerosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155968",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000451",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000451",
    "nando_id": "NANDO:1200025"
  },
  {
    "id": "C0751965",
    "id2": "MedGen UID:155969",
    "medgen_label": "Secondary progressive multiple sclerosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155969",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000450",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000450",
    "nando_id": "NANDO:1200026"
  },
  {
    "id": "C0751967",
    "id2": "MedGen UID:155669",
    "medgen_label": "Relapsing remitting multiple sclerosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155669",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005314",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005314",
    "nando_id": "NANDO:1200024"
  },
  {
    "id": "C0752120",
    "id2": "MedGen UID:155703",
    "medgen_label": "Spinocerebellar ataxia type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155703",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008119",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008119",
    "nando_id": "NANDO:1200045"
  },
  {
    "id": "C0752121",
    "id2": "MedGen UID:155704",
    "medgen_label": "Spinocerebellar ataxia type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155704",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008458",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008458",
    "nando_id": "NANDO:1200046"
  },
  {
    "id": "C0752124",
    "id2": "MedGen UID:148458",
    "medgen_label": "Spinocerebellar ataxia type 6",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/148458",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008457",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008457",
    "nando_id": "NANDO:1200042"
  },
  {
    "id": "C4023588",
    "id2": "MedGen UID:892790",
    "medgen_label": "Abnormality of the gastrointestinal tract",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/892790",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0004335",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004335",
    "nando_id": "NANDO:1100013"
  },
  {
    "id": "C1848533",
    "id2": "MedGen UID:341248",
    "medgen_label": "Familial isolated deficiency of vitamin E",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/341248",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010188",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010188",
    "nando_id": "NANDO:1200050"
  },
  {
    "id": "C0004712",
    "id2": "MedGen UID:498",
    "medgen_label": "Balo concentric sclerosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/498",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016430",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016430",
    "nando_id": "NANDO:1200028"
  },
  {
    "id": "C0007959",
    "id2": "MedGen UID:2980",
    "medgen_label": "Charcot-Marie-Tooth disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/2980",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015626",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015626",
    "nando_id": "NANDO:1200016"
  },
  {
    "id": "C0008626",
    "id2": "MedGen UID:3441",
    "medgen_label": "Congenital chromosomal disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/3441",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019040",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019040",
    "nando_id": "NANDO:1100014"
  },
  {
    "id": "C0220756",
    "id2": "MedGen UID:67399",
    "medgen_label": "Niemann-Pick disease, type C",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/67399",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018982",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018982",
    "nando_id": "NANDO:1200063"
  },
  {
    "id": "C5848259",
    "id2": "MedGen UID:1845578",
    "medgen_label": "Werdnig-Hoffmann disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1845578",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009669",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009669",
    "nando_id": "NANDO:1200004"
  },
  {
    "id": "C0023522",
    "id2": "MedGen UID:6071",
    "medgen_label": "Metachromatic leukodystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6071",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018868",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018868",
    "nando_id": "NANDO:1200078"
  },
  {
    "id": "C0026896",
    "id2": "MedGen UID:7764",
    "medgen_label": "Myasthenia gravis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7764",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009688",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009688",
    "nando_id": "NANDO:1200020"
  },
  {
    "id": "C0027868",
    "id2": "MedGen UID:10323",
    "medgen_label": "Neuromuscular disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10323",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019056",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019056",
    "nando_id": "NANDO:1100001"
  },
  {
    "id": "C0027873",
    "id2": "MedGen UID:45063",
    "medgen_label": "Neuromyelitis optica",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/45063",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019100",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019100",
    "nando_id": "NANDO:1200027"
  },
  {
    "id": "C0268242",
    "id2": "MedGen UID:78650",
    "medgen_label": "Niemann-Pick disease, type A",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78650",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009756",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009756",
    "nando_id": "NANDO:1200061"
  },
  {
    "id": "C0268243",
    "id2": "MedGen UID:78651",
    "medgen_label": "Niemann-Pick disease, type B",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78651",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011871",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011871",
    "nando_id": "NANDO:1200062"
  },
  {
    "id": "C0268252",
    "id2": "MedGen UID:120623",
    "medgen_label": "Adult Krabbe disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120623",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016091",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016091",
    "nando_id": "NANDO:1200077"
  },
  {
    "id": "C0268274",
    "id2": "MedGen UID:78656",
    "medgen_label": "GM2 gangliosidosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78656",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017720",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017720",
    "nando_id": "NANDO:1200070"
  },
  {
    "id": "C0268275",
    "id2": "MedGen UID:78657",
    "medgen_label": "Tay-Sachs disease, variant AB",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78657",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010099",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010099",
    "nando_id": "NANDO:1200073"
  },
  {
    "id": "C0270914",
    "id2": "MedGen UID:124378",
    "medgen_label": "Charcot-Marie-Tooth disease type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/124378",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018993",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018993",
    "nando_id": "NANDO:1200018"
  },
  {
    "id": "C0393538",
    "id2": "MedGen UID:95975",
    "medgen_label": "Spinal muscular atrophy, type II",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/95975",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009673",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009673",
    "nando_id": "NANDO:1200005"
  },
  {
    "id": "C0393547",
    "id2": "MedGen UID:95977",
    "medgen_label": "Bulbospinal muscular atrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/95977",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0016113",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016113",
    "nando_id": "NANDO:1200001"
  },
  {
    "id": "C0393555",
    "id2": "MedGen UID:581445",
    "medgen_label": "Pure hereditary spastic paraplegia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/581445",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015149",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015149",
    "nando_id": "NANDO:1200053"
  },
  {
    "id": "C0393556",
    "id2": "MedGen UID:581446",
    "medgen_label": "Complex hereditary spastic paraplegia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/581446",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015150",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015150",
    "nando_id": "NANDO:1200054"
  },
  {
    "id": "C0393570",
    "id2": "MedGen UID:95979",
    "medgen_label": "Corticobasal degeneration disorder",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/95979",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0022308",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0022308",
    "nando_id": "NANDO:1200011"
  },
  {
    "id": "C0393847",
    "id2": "MedGen UID:581615",
    "medgen_label": "Multifocal motor neuropathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/581615",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018979",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018979",
    "nando_id": "NANDO:1200031"
  },
  {
    "id": "C0398568",
    "id2": "MedGen UID:140765",
    "medgen_label": "McLeod neuroacanthocytosis syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/140765",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018945",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018945",
    "nando_id": "NANDO:1200015"
  },
  {
    "id": "C3472711",
    "id2": "MedGen UID:483339",
    "medgen_label": "Spinocerebellar ataxia type 36",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/483339",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013594",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013594",
    "nando_id": "NANDO:1200048"
  },
  {
    "id": "C0085131",
    "id2": "MedGen UID:43107",
    "medgen_label": "GM1 gangliosidosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/43107",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018149",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018149",
    "nando_id": "NANDO:1200066"
  },
  {
    "id": "C0085404",
    "id2": "MedGen UID:39276",
    "medgen_label": "POEMS syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/39276",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017364",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017364",
    "nando_id": "NANDO:1200033"
  },
  {
    "id": "C0152109",
    "id2": "MedGen UID:101816",
    "medgen_label": "Kugelberg-Welander disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/101816",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009672",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009672",
    "nando_id": "NANDO:1200006"
  },
  {
    "id": "C0154682",
    "id2": "MedGen UID:57591",
    "medgen_label": "Primary lateral sclerosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/57591",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018155",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018155",
    "nando_id": "NANDO:1200008"
  },
  {
    "id": "C0751036",
    "id2": "MedGen UID:155486",
    "medgen_label": "Charcot-Marie-Tooth disease, type I",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155486",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019011",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019011",
    "nando_id": "NANDO:1200017"
  },
  {
    "id": "C1838230",
    "id2": "MedGen UID:325364",
    "medgen_label": "Spinal muscular atrophy, type IV",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/325364",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010056",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010056",
    "nando_id": "NANDO:1200007"
  },
  {
    "id": "C1839259",
    "id2": "MedGen UID:333282",
    "medgen_label": "Kennedy disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/333282",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010735",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010735",
    "nando_id": "NANDO:1200001"
  },
  {
    "id": "C5554234",
    "id2": "MedGen UID:1843304",
    "medgen_label": "Multiple system atrophy, cerebellar type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1843304",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016418",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016418",
    "nando_id": "NANDO:1200035"
  },
  {
    "id": "C5554235",
    "id2": "MedGen UID:1842393",
    "medgen_label": "Multiple system atrophy, parkinsonian type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1842393",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020352",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020352",
    "nando_id": "NANDO:1200036"
  },
  {
    "id": "C0036161",
    "id2": "MedGen UID:11313",
    "medgen_label": "Sandhoff disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/11313",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010006",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010006",
    "nando_id": "NANDO:1200072"
  },
  {
    "id": "C0037773",
    "id2": "MedGen UID:20844",
    "medgen_label": "Hereditary spastic paraplegia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/20844",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019064",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019064",
    "nando_id": "NANDO:1200052"
  },
  {
    "id": "C0038868",
    "id2": "MedGen UID:21026",
    "medgen_label": "Progressive supranuclear palsy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21026",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019037",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019037",
    "nando_id": "NANDO:1200009"
  },
  {
    "id": "C0039373",
    "id2": "MedGen UID:11713",
    "medgen_label": "Tay-Sachs disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/11713",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010100",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010100",
    "nando_id": "NANDO:1200071"
  },
  {
    "id": "C0017205",
    "id2": "MedGen UID:42164",
    "medgen_label": "Gaucher disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/42164",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018150",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018150",
    "nando_id": "NANDO:1200056"
  },
  {
    "id": "C0751273",
    "id2": "MedGen UID:148270",
    "medgen_label": "Infantile Krabbe disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/148270",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016089",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016089",
    "nando_id": "NANDO:1200075"
  },
  {
    "id": "C0751276",
    "id2": "MedGen UID:155528",
    "medgen_label": "Metachromatic leukodystrophy, juvenile type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155528",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009591",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009591",
    "nando_id": "NANDO:1200080"
  },
  {
    "id": "C0751278",
    "id2": "MedGen UID:155529",
    "medgen_label": "Metachromatic leukodystrophy, late infantile form",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155529",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017729",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017729",
    "nando_id": "NANDO:1200079"
  },
  {
    "id": "C0751279",
    "id2": "MedGen UID:199625",
    "medgen_label": "Metachromatic leukodystrophy, adult type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/199625",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017730",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017730",
    "nando_id": "NANDO:1200081"
  },
  {
    "id": "C0751882",
    "id2": "MedGen UID:155650",
    "medgen_label": "Congenital myasthenic syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155650",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018940",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018940",
    "nando_id": "NANDO:1200021"
  },
  {
    "id": "C5680108",
    "id2": "MedGen UID:1826149",
    "medgen_label": "Charcot-Marie-Tooth disease, intermediate type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1826149",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018778",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018778",
    "nando_id": "NANDO:1200019"
  },
  {
    "id": "C5680869",
    "id2": "MedGen UID:1826101",
    "medgen_label": "Niemann-Pick disease type C, adult neurologic onset",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1826101",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016310",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016310",
    "nando_id": "NANDO:1200065"
  },
  {
    "id": "CN294033",
    "id2": "MedGen UID:976451",
    "medgen_label": "Neuroacanthocytosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/976451",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016987",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016987",
    "nando_id": "NANDO:1200013"
  },
  {
    "id": "C0162674",
    "id2": "MedGen UID:102439",
    "medgen_label": "Progressive external ophthalmoplegia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/102439",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005181",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005181",
    "nando_id": "NANDO:1200174"
  },
  {
    "id": "C2673377",
    "id2": "MedGen UID:435914",
    "medgen_label": "Mucolipidosis type II",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/435914",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009650",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009650",
    "nando_id": "NANDO:1200124"
  },
  {
    "id": "C0024748",
    "id2": "MedGen UID:7467",
    "medgen_label": "Deficiency of alpha-mannosidase",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7467",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009561",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009561",
    "nando_id": "NANDO:1200126"
  },
  {
    "id": "C0268225",
    "id2": "MedGen UID:78649",
    "medgen_label": "Aspartylglucosaminuria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78649",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008830",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008830",
    "nando_id": "NANDO:1200133"
  },
  {
    "id": "C0268255",
    "id2": "MedGen UID:78654",
    "medgen_label": "Farber lipogranulomatosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78654",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009218",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009218",
    "nando_id": "NANDO:1200086"
  },
  {
    "id": "C0268262",
    "id2": "MedGen UID:120624",
    "medgen_label": "Sphingolipid activator protein 1 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120624",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009590",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009590",
    "nando_id": "NANDO:1200082"
  },
  {
    "id": "C0268626",
    "id2": "MedGen UID:75701",
    "medgen_label": "Juvenile nephropathic cystinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75701",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009066",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009066",
    "nando_id": "NANDO:1200163"
  },
  {
    "id": "C0086647",
    "id2": "MedGen UID:39264",
    "medgen_label": "Mucopolysaccharidosis, MPS-III-A",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/39264",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009655",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009655",
    "nando_id": "NANDO:1200101"
  },
  {
    "id": "C0086648",
    "id2": "MedGen UID:88601",
    "medgen_label": "Mucopolysaccharidosis, MPS-III-B",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/88601",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009656",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009656",
    "nando_id": "NANDO:1200102"
  },
  {
    "id": "C0086649",
    "id2": "MedGen UID:39477",
    "medgen_label": "Mucopolysaccharidosis, MPS-III-C",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/39477",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009657",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009657",
    "nando_id": "NANDO:1200103"
  },
  {
    "id": "C0086650",
    "id2": "MedGen UID:88602",
    "medgen_label": "Mucopolysaccharidosis, MPS-III-D",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/88602",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009658",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009658",
    "nando_id": "NANDO:1200104"
  },
  {
    "id": "C0086651",
    "id2": "MedGen UID:43375",
    "medgen_label": "Mucopolysaccharidosis, MPS-IV-A",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/43375",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009659",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009659",
    "nando_id": "NANDO:1200106"
  },
  {
    "id": "C0086652",
    "id2": "MedGen UID:43376",
    "medgen_label": "Mucopolysaccharidosis, MPS-IV-B",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/43376",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009660",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009660",
    "nando_id": "NANDO:1200107"
  },
  {
    "id": "C1876161",
    "id2": "MedGen UID:406281",
    "medgen_label": "Neuronal ceroid lipofuscinosis 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/406281",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0008769",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008769",
    "nando_id": "NANDO:1200153"
  },
  {
    "id": "C2931013",
    "id2": "MedGen UID:419313",
    "medgen_label": "Ocular cystinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/419313",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009064",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009064",
    "nando_id": "NANDO:1200164"
  },
  {
    "id": "C0016788",
    "id2": "MedGen UID:5288",
    "medgen_label": "Fucosidosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5288",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009254",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009254",
    "nando_id": "NANDO:1200130"
  },
  {
    "id": "C0017921",
    "id2": "MedGen UID:5340",
    "medgen_label": "Glycogen storage disease, type II",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5340",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009290",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009290",
    "nando_id": "NANDO:1200138"
  },
  {
    "id": "C1456275",
    "id2": "MedGen UID:1778113",
    "medgen_label": "Inborn mitochondrial metabolism disorder",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1778113",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0004069",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004069",
    "nando_id": "NANDO:1200173"
  },
  {
    "id": "C4048196",
    "id2": "MedGen UID:888408",
    "medgen_label": "Beta-D-mannosidosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/888408",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009562",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009562",
    "nando_id": "NANDO:1200129"
  },
  {
    "id": "C1850451",
    "id2": "MedGen UID:340540",
    "medgen_label": "Neuronal ceroid lipofuscinosis 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/340540",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009744",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009744",
    "nando_id": "NANDO:1200152"
  },
  {
    "id": "C0002986",
    "id2": "MedGen UID:8083",
    "medgen_label": "Fabry disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/8083",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010526",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010526",
    "nando_id": "NANDO:1200157"
  },
  {
    "id": "C0008384",
    "id2": "MedGen UID:40266",
    "medgen_label": "Cholesteryl ester storage disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/40266",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019149",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019149",
    "nando_id": "NANDO:1200144"
  },
  {
    "id": "C0162309",
    "id2": "MedGen UID:57667",
    "medgen_label": "Adrenoleukodystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/57667",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018544",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018544",
    "nando_id": "NANDO:1200165"
  },
  {
    "id": "C0162671",
    "id2": "MedGen UID:56485",
    "medgen_label": "Juvenile myopathy, encephalopathy, lactic acidosis AND stroke",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/56485",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010789",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010789",
    "nando_id": "NANDO:1200176"
  },
  {
    "id": "C0162672",
    "id2": "MedGen UID:56486",
    "medgen_label": "MERRF syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/56486",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010790",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010790",
    "nando_id": "NANDO:1200177"
  },
  {
    "id": "C2026514",
    "id2": "MedGen UID:1708324",
    "medgen_label": "X-linked cerebral adrenoleukodystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1708324",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010247",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010247",
    "nando_id": "NANDO:1200166"
  },
  {
    "id": "C2931251",
    "id2": "MedGen UID:419756",
    "medgen_label": "Alpha-mannosidosis type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/419756",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0022424",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0022424",
    "nando_id": "NANDO:1200127"
  },
  {
    "id": "C2931872",
    "id2": "MedGen UID:419512",
    "medgen_label": "Free sialic acid storage disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/419512",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019366",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019366",
    "nando_id": "NANDO:1200146"
  },
  {
    "id": "C5848084",
    "id2": "MedGen UID:1845666",
    "medgen_label": "Alpha-N-acetylgalactosaminidase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1845666",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017779",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017779",
    "nando_id": "NANDO:1200134"
  },
  {
    "id": "C0022797",
    "id2": "MedGen UID:7230",
    "medgen_label": "Adult neuronal ceroid lipofuscinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7230",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019260",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019260",
    "nando_id": "NANDO:1200155"
  },
  {
    "id": "C0023264",
    "id2": "MedGen UID:44095",
    "medgen_label": "Leigh syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44095",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009723",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009723",
    "nando_id": "NANDO:1200175"
  },
  {
    "id": "C0023806",
    "id2": "MedGen UID:44174",
    "medgen_label": "Sialidosis type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44174",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019346",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019346",
    "nando_id": "NANDO:1200117"
  },
  {
    "id": "C0026705",
    "id2": "MedGen UID:7734",
    "medgen_label": "Mucopolysaccharidosis, MPS-II",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7734",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010674",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010674",
    "nando_id": "NANDO:1200097"
  },
  {
    "id": "C0026706",
    "id2": "MedGen UID:6452",
    "medgen_label": "Sanfilippo syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6452",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018937",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018937",
    "nando_id": "NANDO:1200100"
  },
  {
    "id": "C0026707",
    "id2": "MedGen UID:44513",
    "medgen_label": "Morquio syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44513",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018938",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018938",
    "nando_id": "NANDO:1200105"
  },
  {
    "id": "C0026708",
    "id2": "MedGen UID:6453",
    "medgen_label": "Mucopolysaccharidosis, MPS-I-S",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6453",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011760",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011760",
    "nando_id": "NANDO:1200095"
  },
  {
    "id": "C0026709",
    "id2": "MedGen UID:44514",
    "medgen_label": "Mucopolysaccharidosis type 6",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44514",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009661",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009661",
    "nando_id": "NANDO:1200108"
  },
  {
    "id": "C0026709",
    "id2": "MedGen UID:44514",
    "medgen_label": "Mucopolysaccharidosis type 6",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44514",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009661",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009661",
    "nando_id": "NANDO:1200109"
  },
  {
    "id": "C0026709",
    "id2": "MedGen UID:44514",
    "medgen_label": "Mucopolysaccharidosis type 6",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44514",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009661",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009661",
    "nando_id": "NANDO:1200110"
  },
  {
    "id": "C0027877",
    "id2": "MedGen UID:10326",
    "medgen_label": "Neuronal ceroid lipofuscinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10326",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016295",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016295",
    "nando_id": "NANDO:1200150"
  },
  {
    "id": "C0268226",
    "id2": "MedGen UID:120621",
    "medgen_label": "Sialidosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120621",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017734",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017734",
    "nando_id": "NANDO:1200116"
  },
  {
    "id": "C0268233",
    "id2": "MedGen UID:82779",
    "medgen_label": "Combined deficiency of sialidase AND beta galactosidase",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82779",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009737",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009737",
    "nando_id": "NANDO:1200119"
  },
  {
    "id": "C0268263",
    "id2": "MedGen UID:75664",
    "medgen_label": "Multiple sulfatase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75664",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010088",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010088",
    "nando_id": "NANDO:1200083"
  },
  {
    "id": "C0268263",
    "id2": "MedGen UID:75664",
    "medgen_label": "Multiple sulfatase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75664",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0010088",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010088",
    "nando_id": "NANDO:1200084"
  },
  {
    "id": "C0268263",
    "id2": "MedGen UID:75664",
    "medgen_label": "Multiple sulfatase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75664",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0010088",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010088",
    "nando_id": "NANDO:1200085"
  },
  {
    "id": "C0268281",
    "id2": "MedGen UID:75666",
    "medgen_label": "Infantile neuronal ceroid lipofuscinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75666",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019261",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019261",
    "nando_id": "NANDO:1200152"
  },
  {
    "id": "C1096902",
    "id2": "MedGen UID:203367",
    "medgen_label": "Sialic acid storage disease, severe infantile type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/203367",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010027",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010027",
    "nando_id": "NANDO:1200147"
  },
  {
    "id": "C3537440",
    "id2": "MedGen UID:760976",
    "medgen_label": "Infantile nephropathic cystinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/760976",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018467",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018467",
    "nando_id": "NANDO:1200162"
  },
  {
    "id": "C4282398",
    "id2": "MedGen UID:924303",
    "medgen_label": "Sialidosis type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/924303",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009738",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009738",
    "nando_id": "NANDO:1200118"
  },
  {
    "id": "C4282398",
    "id2": "MedGen UID:924303",
    "medgen_label": "Sialidosis type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/924303",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009738",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009738",
    "nando_id": "NANDO:1200120"
  },
  {
    "id": "C0085132",
    "id2": "MedGen UID:43108",
    "medgen_label": "Mucopolysaccharidosis type 7",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/43108",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009662",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009662",
    "nando_id": "NANDO:1200111"
  },
  {
    "id": "C0086431",
    "id2": "MedGen UID:88566",
    "medgen_label": "Mucopolysaccharidosis, MPS-I-H/S",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/88566",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011759",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011759",
    "nando_id": "NANDO:1200096"
  },
  {
    "id": "C0086795",
    "id2": "MedGen UID:39698",
    "medgen_label": "Hurler syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/39698",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011758",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011758",
    "nando_id": "NANDO:1200094"
  },
  {
    "id": "C0342841",
    "id2": "MedGen UID:575246",
    "medgen_label": "Mucopolysaccharidosis type 2, severe form",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/575246",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016315",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016315",
    "nando_id": "NANDO:1200098"
  },
  {
    "id": "C1836522",
    "id2": "MedGen UID:324539",
    "medgen_label": "Alpha-N-acetylgalactosaminidase deficiency type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/324539",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012222",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012222",
    "nando_id": "NANDO:1200136"
  },
  {
    "id": "C1836544",
    "id2": "MedGen UID:373113",
    "medgen_label": "Alpha-N-acetylgalactosaminidase deficiency type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/373113",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012221",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012221",
    "nando_id": "NANDO:1200135"
  },
  {
    "id": "C1838979",
    "id2": "MedGen UID:374101",
    "medgen_label": "Mitochondrial complex I deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/374101",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0100133",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0100133",
    "nando_id": "NANDO:1200180"
  },
  {
    "id": "C3888924",
    "id2": "MedGen UID:923868",
    "medgen_label": "Glycogen storage disease due to acid maltase deficiency, infantile onset",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/923868",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017694",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017694",
    "nando_id": "NANDO:1200139"
  },
  {
    "id": "C0033788",
    "id2": "MedGen UID:10988",
    "medgen_label": "Pseudo-Hurler polydystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10988",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018931",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018931",
    "nando_id": "NANDO:1200125"
  },
  {
    "id": "C0043208",
    "id2": "MedGen UID:53088",
    "medgen_label": "Wolman disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/53088",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0019148",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019148",
    "nando_id": "NANDO:1200142"
  },
  {
    "id": "C0043208",
    "id2": "MedGen UID:53088",
    "medgen_label": "Wolman disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/53088",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019148",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019148",
    "nando_id": "NANDO:1200143"
  },
  {
    "id": "C2931187",
    "id2": "MedGen UID:419735",
    "medgen_label": "Nephropathic cystinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/419735",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0100151",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0100151",
    "nando_id": "NANDO:1200162"
  },
  {
    "id": "C4316899",
    "id2": "MedGen UID:1384792",
    "medgen_label": "Cystinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1384792",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016239",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016239",
    "nando_id": "NANDO:1200161"
  },
  {
    "id": "C5437471",
    "id2": "MedGen UID:1772900",
    "medgen_label": "Alpha-N-acetylgalactosaminidase deficiency type 3",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1772900",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019264",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019264",
    "nando_id": "NANDO:1200137"
  },
  {
    "id": "C0022340",
    "id2": "MedGen UID:9589",
    "medgen_label": "Late-infantile neuronal ceroid lipofuscinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9589",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015674",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015674",
    "nando_id": "NANDO:1200153"
  },
  {
    "id": "C0751651",
    "id2": "MedGen UID:155901",
    "medgen_label": "Mitochondrial disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155901",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0044970",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0044970",
    "nando_id": "NANDO:1200173"
  },
  {
    "id": "C1291490",
    "id2": "MedGen UID:226942",
    "medgen_label": "Deficiency of hyaluronoglucosaminidase",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/226942",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011093",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011093",
    "nando_id": "NANDO:1200115"
  },
  {
    "id": "C1527231",
    "id2": "MedGen UID:315918",
    "medgen_label": "Adrenomyeloneuropathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/315918",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015339",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015339",
    "nando_id": "NANDO:1200168"
  },
  {
    "id": "C5679815",
    "id2": "MedGen UID:1826165",
    "medgen_label": "Mucopolysaccharidosis type 2, attenuated form",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1826165",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016316",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016316",
    "nando_id": "NANDO:1200099"
  },
  {
    "id": "C5679974",
    "id2": "MedGen UID:1843432",
    "medgen_label": "Alpha-mannosidosis, adult form",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1843432",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017733",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017733",
    "nando_id": "NANDO:1200128"
  },
  {
    "id": "C5681076",
    "id2": "MedGen UID:1843217",
    "medgen_label": "Intermediate severe Salla disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1843217",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017737",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017737",
    "nando_id": "NANDO:1200148"
  },
  {
    "id": "CN257533",
    "id2": "MedGen UID:940569",
    "medgen_label": "Mitochondrial complex I deficiency, nuclear type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/940569",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0100224",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0100224",
    "nando_id": "NANDO:1200180"
  },
  {
    "id": "CN293564",
    "id2": "MedGen UID:978346",
    "medgen_label": "Juvenile neuronal ceroid lipofuscinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/978346",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019262",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019262",
    "nando_id": "NANDO:1200154"
  },
  {
    "id": "C1834014",
    "id2": "MedGen UID:320250",
    "medgen_label": "Oculopharyngodistal myopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/320250",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0025193",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0025193",
    "nando_id": "NANDO:1200219"
  },
  {
    "id": "C1834674",
    "id2": "MedGen UID:331805",
    "medgen_label": "Bethlem myopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/331805",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008029",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008029",
    "nando_id": "NANDO:1200220"
  },
  {
    "id": "C1852467",
    "id2": "MedGen UID:377682",
    "medgen_label": "Creutzfeldt-Jakob disease, sporadic",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/377682",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016079",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016079",
    "nando_id": "NANDO:1200187"
  },
  {
    "id": "C1853926",
    "id2": "MedGen UID:381298",
    "medgen_label": "GNE myopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/381298",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011603",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011603",
    "nando_id": "NANDO:1200218"
  },
  {
    "id": "C0003509",
    "id2": "MedGen UID:8154",
    "medgen_label": "Aortitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/8154",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0006656",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006656",
    "nando_id": "NANDO:1200251"
  },
  {
    "id": "C0008728",
    "id2": "MedGen UID:3088",
    "medgen_label": "Eosinophilic granulomatosis with polyangiitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/3088",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015943",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015943",
    "nando_id": "NANDO:1200264"
  },
  {
    "id": "C0162534",
    "id2": "MedGen UID:56445",
    "medgen_label": "Prion disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/56445",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005429",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005429",
    "nando_id": "NANDO:1200186"
  },
  {
    "id": "C0162678",
    "id2": "MedGen UID:58149",
    "medgen_label": "Neurofibromatosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/58149",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0021061",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0021061",
    "nando_id": "NANDO:1200225"
  },
  {
    "id": "C0162678",
    "id2": "MedGen UID:58149",
    "medgen_label": "Neurofibromatosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/58149",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0021061",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0021061",
    "nando_id": "NANDO:1200226"
  },
  {
    "id": "C0162678",
    "id2": "MedGen UID:58149",
    "medgen_label": "Neurofibromatosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/58149",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0021061",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0021061",
    "nando_id": "NANDO:1200227"
  },
  {
    "id": "C0206042",
    "id2": "MedGen UID:104768",
    "medgen_label": "Fatal familial insomnia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/104768",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010808",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010808",
    "nando_id": "NANDO:1200191"
  },
  {
    "id": "C0206245",
    "id2": "MedGen UID:104815",
    "medgen_label": "Familial amyloid neuropathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/104815",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0007100",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007100",
    "nando_id": "NANDO:1200214"
  },
  {
    "id": "C0406557",
    "id2": "MedGen UID:96060",
    "medgen_label": "Kindler syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/96060",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008260",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008260",
    "nando_id": "NANDO:1200239"
  },
  {
    "id": "C0409980",
    "id2": "MedGen UID:592740",
    "medgen_label": "Primary antiphospholipid syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/592740",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005204",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005204",
    "nando_id": "NANDO:1200267"
  },
  {
    "id": "C0410179",
    "id2": "MedGen UID:98046",
    "medgen_label": "Ullrich congenital muscular dystrophy 1A",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/98046",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009681",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009681",
    "nando_id": "NANDO:1200215"
  },
  {
    "id": "C2347126",
    "id2": "MedGen UID:389393",
    "medgen_label": "Microscopic polyangiitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/389393",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019124",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019124",
    "nando_id": "NANDO:1200262"
  },
  {
    "id": "C2349757",
    "id2": "MedGen UID:908476",
    "medgen_label": "Iatrogenic Creutzfeldt-Jakob disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/908476",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0034976",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0034976",
    "nando_id": "NANDO:1200193"
  },
  {
    "id": "C5231388",
    "id2": "MedGen UID:1684682",
    "medgen_label": "Oculopharyngodistal myopathy 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1684682",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0020793",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020793",
    "nando_id": "NANDO:1200219"
  },
  {
    "id": "C0023524",
    "id2": "MedGen UID:7327",
    "medgen_label": "Progressive multifocal leukoencephalopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7327",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016318",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016318",
    "nando_id": "NANDO:1200205"
  },
  {
    "id": "C0024141",
    "id2": "MedGen UID:6146",
    "medgen_label": "Systemic lupus erythematosus",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6146",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007915",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007915",
    "nando_id": "NANDO:1200272"
  },
  {
    "id": "C0026654",
    "id2": "MedGen UID:7726",
    "medgen_label": "Moyamoya disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7726",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016820",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016820",
    "nando_id": "NANDO:1200183"
  },
  {
    "id": "C0027831",
    "id2": "MedGen UID:18013",
    "medgen_label": "Neurofibromatosis, type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/18013",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018975",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018975",
    "nando_id": "NANDO:1200226"
  },
  {
    "id": "C0027831",
    "id2": "MedGen UID:18013",
    "medgen_label": "Neurofibromatosis, type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/18013",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018975",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018975",
    "nando_id": "NANDO:1200225"
  },
  {
    "id": "C0027832",
    "id2": "MedGen UID:18014",
    "medgen_label": "Neurofibromatosis, type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/18014",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007039",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007039",
    "nando_id": "NANDO:1200227"
  },
  {
    "id": "C0030481",
    "id2": "MedGen UID:18298",
    "medgen_label": "HTLV-1-associated myelopathy-tropical spastic paraparesis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/18298",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008039",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008039",
    "nando_id": "NANDO:1200206"
  },
  {
    "id": "C0030807",
    "id2": "MedGen UID:45369",
    "medgen_label": "Pemphigus",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/45369",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006594",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006594",
    "nando_id": "NANDO:1200228"
  },
  {
    "id": "C0030809",
    "id2": "MedGen UID:10621",
    "medgen_label": "Pemphigus vulgaris",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10621",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008219",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008219",
    "nando_id": "NANDO:1200229"
  },
  {
    "id": "C0031036",
    "id2": "MedGen UID:14681",
    "medgen_label": "Polyarteritis nodosa",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/14681",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019170",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019170",
    "nando_id": "NANDO:1200261"
  },
  {
    "id": "C0268381",
    "id2": "MedGen UID:75674",
    "medgen_label": "AL amyloidosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75674",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019438",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019438",
    "nando_id": "NANDO:1200211"
  },
  {
    "id": "C0376329",
    "id2": "MedGen UID:138163",
    "medgen_label": "Variant Creutzfeldt-Jakob disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/138163",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007012",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007012",
    "nando_id": "NANDO:1200194"
  },
  {
    "id": "C0392439",
    "id2": "MedGen UID:581114",
    "medgen_label": "Acrodermatitis continua suppurativa of Hallopeau",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/581114",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013626",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013626",
    "nando_id": "NANDO:1200244"
  },
  {
    "id": "C1112570",
    "id2": "MedGen UID:798302",
    "medgen_label": "Paraneoplastic pemphigus",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/798302",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018974",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018974",
    "nando_id": "NANDO:1200231"
  },
  {
    "id": "C3495801",
    "id2": "MedGen UID:811223",
    "medgen_label": "Granulomatosis with polyangiitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/811223",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012105",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012105",
    "nando_id": "NANDO:1200263"
  },
  {
    "id": "C3662487",
    "id2": "MedGen UID:783641",
    "medgen_label": "Catastrophic antiphospholipid syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/783641",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018737",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018737",
    "nando_id": "NANDO:1200270"
  },
  {
    "id": "C0079298",
    "id2": "MedGen UID:86896",
    "medgen_label": "Epidermolysis bullosa simplex",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/86896",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017610",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017610",
    "nando_id": "NANDO:1200235"
  },
  {
    "id": "C0079301",
    "id2": "MedGen UID:86898",
    "medgen_label": "Junctional epidermolysis bullosa",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/86898",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017612",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017612",
    "nando_id": "NANDO:1200236"
  },
  {
    "id": "C0079474",
    "id2": "MedGen UID:36311",
    "medgen_label": "Recessive dystrophic epidermolysis bullosa",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/36311",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009179",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009179",
    "nando_id": "NANDO:1200238"
  },
  {
    "id": "C0152081",
    "id2": "MedGen UID:508876",
    "medgen_label": "Pustular psoriasis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/508876",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0022205",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0022205",
    "nando_id": "NANDO:1200240"
  },
  {
    "id": "C0342623",
    "id2": "MedGen UID:87446",
    "medgen_label": "Wild type ATTR amyloidosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/87446",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018018",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018018",
    "nando_id": "NANDO:1200212"
  },
  {
    "id": "C1839615",
    "id2": "MedGen UID:374264",
    "medgen_label": "X-linked myopathy with excessive autophagy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/374264",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010684",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010684",
    "nando_id": "NANDO:1200223"
  },
  {
    "id": "C4551624",
    "id2": "MedGen UID:1637664",
    "medgen_label": "Idiopathic basal ganglia calcification 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1637664",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0024538",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0024538",
    "nando_id": "NANDO:1200208"
  },
  {
    "id": "C4551860",
    "id2": "MedGen UID:1642667",
    "medgen_label": "Ullrich congenital muscular dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1642667",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000355",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000355",
    "nando_id": "NANDO:1200215"
  },
  {
    "id": "C5553104",
    "id2": "MedGen UID:1790866",
    "medgen_label": "Miyoshi myopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1790866",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009685",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009685",
    "nando_id": "NANDO:1200217"
  },
  {
    "id": "C0036391",
    "id2": "MedGen UID:19892",
    "medgen_label": "Schwartz-Jampel syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/19892",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009717",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009717",
    "nando_id": "NANDO:1200224"
  },
  {
    "id": "C0038325",
    "id2": "MedGen UID:20955",
    "medgen_label": "Stevens-Johnson syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/20955",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018229",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018229",
    "nando_id": "NANDO:1200245"
  },
  {
    "id": "C0038522",
    "id2": "MedGen UID:52527",
    "medgen_label": "Subacute sclerosing panencephalitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/52527",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009835",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009835",
    "nando_id": "NANDO:1200195"
  },
  {
    "id": "C0038522",
    "id2": "MedGen UID:52527",
    "medgen_label": "Subacute sclerosing panencephalitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/52527",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009835",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009835",
    "nando_id": "NANDO:1200196"
  },
  {
    "id": "C0038522",
    "id2": "MedGen UID:52527",
    "medgen_label": "Subacute sclerosing panencephalitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/52527",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009835",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009835",
    "nando_id": "NANDO:1200198"
  },
  {
    "id": "C0039263",
    "id2": "MedGen UID:21458",
    "medgen_label": "Takayasu arteritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21458",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017991",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017991",
    "nando_id": "NANDO:1200251"
  },
  {
    "id": "C0040021",
    "id2": "MedGen UID:21531",
    "medgen_label": "Thromboangiitis obliterans",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21531",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008889",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008889",
    "nando_id": "NANDO:1200266"
  },
  {
    "id": "C0281479",
    "id2": "MedGen UID:129028",
    "medgen_label": "Primary systemic amyloidosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/129028",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017816",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017816",
    "nando_id": "NANDO:1200209"
  },
  {
    "id": "C1956391",
    "id2": "MedGen UID:365495",
    "medgen_label": "Temporal arteritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/365495",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008538",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008538",
    "nando_id": "NANDO:1200258"
  },
  {
    "id": "C5399975",
    "id2": "MedGen UID:1728314",
    "medgen_label": "Myopathy, distal, with rimmed vacuoles",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1728314",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0014945",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014945",
    "nando_id": "NANDO:1200218"
  },
  {
    "id": "C0014518",
    "id2": "MedGen UID:4501",
    "medgen_label": "Toxic epidermal necrolysis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/4501",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019810",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019810",
    "nando_id": "NANDO:1200246"
  },
  {
    "id": "C0014527",
    "id2": "MedGen UID:41832",
    "medgen_label": "Epidermolysis bullosa",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/41832",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006541",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006541",
    "nando_id": "NANDO:1200234"
  },
  {
    "id": "C0017495",
    "id2": "MedGen UID:4886",
    "medgen_label": "Gerstmann-Straussler-Scheinker syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/4886",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007656",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007656",
    "nando_id": "NANDO:1200190"
  },
  {
    "id": "C0238190",
    "id2": "MedGen UID:68659",
    "medgen_label": "Inclusion body myositis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/68659",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0007827",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007827",
    "nando_id": "NANDO:1200218"
  },
  {
    "id": "C0240903",
    "id2": "MedGen UID:69122",
    "medgen_label": "Rheumatoid vasculitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/69122",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0043267",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0043267",
    "nando_id": "NANDO:1200265"
  },
  {
    "id": "C0263312",
    "id2": "MedGen UID:537812",
    "medgen_label": "Pemphigus erythematosus",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/537812",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019323",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019323",
    "nando_id": "NANDO:1200233"
  },
  {
    "id": "C0263313",
    "id2": "MedGen UID:75513",
    "medgen_label": "Pemphigus foliaceus",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75513",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019324",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019324",
    "nando_id": "NANDO:1200230"
  },
  {
    "id": "C0263316",
    "id2": "MedGen UID:537814",
    "medgen_label": "Pemphigus vegetans",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/537814",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019322",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019322",
    "nando_id": "NANDO:1200232"
  },
  {
    "id": "C0751254",
    "id2": "MedGen UID:155837",
    "medgen_label": "Inherited Creutzfeldt-Jakob disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155837",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007403",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007403",
    "nando_id": "NANDO:1200189"
  },
  {
    "id": "C0751336",
    "id2": "MedGen UID:155541",
    "medgen_label": "Distal myopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155541",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018949",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018949",
    "nando_id": "NANDO:1200216"
  },
  {
    "id": "C0878677",
    "id2": "MedGen UID:209235",
    "medgen_label": "Danon disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/209235",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010281",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010281",
    "nando_id": "NANDO:1200222"
  },
  {
    "id": "C1314968",
    "id2": "MedGen UID:727290",
    "medgen_label": "Impetigo herpetiformis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/727290",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0004591",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004591",
    "nando_id": "NANDO:1200243"
  },
  {
    "id": "C5681100",
    "id2": "MedGen UID:1826177",
    "medgen_label": "Acquired Creutzfeldt-Jakob disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1826177",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018686",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018686",
    "nando_id": "NANDO:1200192"
  },
  {
    "id": "CN263207",
    "id2": "MedGen UID:946235",
    "medgen_label": "Bilateral striopallidodentate calcinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/946235",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008947",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008947",
    "nando_id": "NANDO:1200207"
  },
  {
    "id": "C1852700",
    "id2": "MedGen UID:343867",
    "medgen_label": "C1 inhibitor deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/343867",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0007361",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007361",
    "nando_id": "NANDO:1200365"
  },
  {
    "id": "C0004135",
    "id2": "MedGen UID:439",
    "medgen_label": "Ataxia-telangiectasia syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/439",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008840",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008840",
    "nando_id": "NANDO:1200331"
  },
  {
    "id": "C0004943",
    "id2": "MedGen UID:2568",
    "medgen_label": "Behcet disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/2568",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007191",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007191",
    "nando_id": "NANDO:1200284"
  },
  {
    "id": "C0005859",
    "id2": "MedGen UID:2685",
    "medgen_label": "Bloom syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/2685",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008876",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008876",
    "nando_id": "NANDO:1200333"
  },
  {
    "id": "C0007194",
    "id2": "MedGen UID:2881",
    "medgen_label": "Hypertrophic cardiomyopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/2881",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005045",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005045",
    "nando_id": "NANDO:1200286"
  },
  {
    "id": "C0007194",
    "id2": "MedGen UID:2881",
    "medgen_label": "Hypertrophic cardiomyopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/2881",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0005045",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005045",
    "nando_id": "NANDO:1200288"
  },
  {
    "id": "C0007196",
    "id2": "MedGen UID:40111",
    "medgen_label": "Restrictive cardiomyopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/40111",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005201",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005201",
    "nando_id": "NANDO:1200292"
  },
  {
    "id": "C0007196",
    "id2": "MedGen UID:40111",
    "medgen_label": "Restrictive cardiomyopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/40111",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0005201",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005201",
    "nando_id": "NANDO:1200293"
  },
  {
    "id": "C0007965",
    "id2": "MedGen UID:3347",
    "medgen_label": "Chédiak-Higashi syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/3347",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008963",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008963",
    "nando_id": "NANDO:1200350"
  },
  {
    "id": "C0012236",
    "id2": "MedGen UID:4297",
    "medgen_label": "DiGeorge syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/4297",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0008564",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008564",
    "nando_id": "NANDO:1200339"
  },
  {
    "id": "C0220704",
    "id2": "MedGen UID:65085",
    "medgen_label": "Velocardiofacial syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/65085",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0008644",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008644",
    "nando_id": "NANDO:1200339"
  },
  {
    "id": "C0221023",
    "id2": "MedGen UID:65121",
    "medgen_label": "Cyclical neutropenia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/65121",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008090",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008090",
    "nando_id": "NANDO:1200354"
  },
  {
    "id": "C0221026",
    "id2": "MedGen UID:65123",
    "medgen_label": "X-linked agammaglobulinemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/65123",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010421",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010421",
    "nando_id": "NANDO:1200343"
  },
  {
    "id": "C2931418",
    "id2": "MedGen UID:444051",
    "medgen_label": "MHC class II deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/444051",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008855",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008855",
    "nando_id": "NANDO:1200329"
  },
  {
    "id": "C0026272",
    "id2": "MedGen UID:10069",
    "medgen_label": "Mixed connective tissue disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10069",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005854",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005854",
    "nando_id": "NANDO:1200278"
  },
  {
    "id": "C0398595",
    "id2": "MedGen UID:96015",
    "medgen_label": "Myeloperoxidase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/96015",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009694",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009694",
    "nando_id": "NANDO:1200358"
  },
  {
    "id": "C0398650",
    "id2": "MedGen UID:584986",
    "medgen_label": "Autoimmune thrombocytopenic purpura",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/584986",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008558",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008558",
    "nando_id": "NANDO:1200315"
  },
  {
    "id": "C0398686",
    "id2": "MedGen UID:585013",
    "medgen_label": "Inborn error of immunity",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/585013",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0003778",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003778",
    "nando_id": "NANDO:1200320"
  },
  {
    "id": "C0398788",
    "id2": "MedGen UID:140770",
    "medgen_label": "Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/140770",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000133",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000133",
    "nando_id": "NANDO:1200334"
  },
  {
    "id": "C0398791",
    "id2": "MedGen UID:140771",
    "medgen_label": "Microcephaly, normal intelligence and immunodeficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/140771",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009623",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009623",
    "nando_id": "NANDO:1200332"
  },
  {
    "id": "C0549463",
    "id2": "MedGen UID:107498",
    "medgen_label": "X-linked lymphoproliferative syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/107498",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010627",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010627",
    "nando_id": "NANDO:1200351"
  },
  {
    "id": "C1268935",
    "id2": "MedGen UID:224783",
    "medgen_label": "Upshaw-Schulman syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/224783",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010122",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010122",
    "nando_id": "NANDO:1200317"
  },
  {
    "id": "C1279481",
    "id2": "MedGen UID:220906",
    "medgen_label": "X-linked severe combined immunodeficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/220906",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010315",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010315",
    "nando_id": "NANDO:1200321"
  },
  {
    "id": "C1856128",
    "id2": "MedGen UID:344659",
    "medgen_label": "Hepatic veno-occlusive disease-immunodeficiency syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/344659",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009338",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009338",
    "nando_id": "NANDO:1200341"
  },
  {
    "id": "C1858266",
    "id2": "MedGen UID:346868",
    "medgen_label": "MHC class I deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/346868",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011476",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011476",
    "nando_id": "NANDO:1200328"
  },
  {
    "id": "C1863236",
    "id2": "MedGen UID:354935",
    "medgen_label": "Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/354935",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007064",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007064",
    "nando_id": "NANDO:1200323"
  },
  {
    "id": "C1846006",
    "id2": "MedGen UID:375786",
    "medgen_label": "Ectodermal dysplasia and immune deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/375786",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010293",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010293",
    "nando_id": "NANDO:1200360"
  },
  {
    "id": "C5574950",
    "id2": "MedGen UID:1802991",
    "medgen_label": "Netherton syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1802991",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009735",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009735",
    "nando_id": "NANDO:1200338"
  },
  {
    "id": "C5575025",
    "id2": "MedGen UID:1809040",
    "medgen_label": "Combined immunodeficiency due to ZAP70 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1809040",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010023",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010023",
    "nando_id": "NANDO:1200327"
  },
  {
    "id": "C0036421",
    "id2": "MedGen UID:19897",
    "medgen_label": "Systemic sclerosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/19897",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005100",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005100",
    "nando_id": "NANDO:1200277"
  },
  {
    "id": "C0043194",
    "id2": "MedGen UID:21921",
    "medgen_label": "Wiskott-Aldrich syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21921",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010518",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010518",
    "nando_id": "NANDO:1200330"
  },
  {
    "id": "C0272167",
    "id2": "MedGen UID:124417",
    "medgen_label": "Reticular dysgenesis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/124417",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009973",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009973",
    "nando_id": "NANDO:1200322"
  },
  {
    "id": "C0272170",
    "id2": "MedGen UID:124418",
    "medgen_label": "Shwachman syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/124418",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009833",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009833",
    "nando_id": "NANDO:1200356"
  },
  {
    "id": "C0272236",
    "id2": "MedGen UID:124420",
    "medgen_label": "Hyperimmunoglobulin M syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/124420",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0003947",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003947",
    "nando_id": "NANDO:1200345"
  },
  {
    "id": "C0272242",
    "id2": "MedGen UID:82898",
    "medgen_label": "Reduced circulating complement concentration",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82898",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0003832",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003832",
    "nando_id": "NANDO:1200364"
  },
  {
    "id": "C2700553",
    "id2": "MedGen UID:398130",
    "medgen_label": "Histiocytic medullary reticulosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/398130",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011338",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011338",
    "nando_id": "NANDO:1200324"
  },
  {
    "id": "C0017661",
    "id2": "MedGen UID:9032",
    "medgen_label": "IgA glomerulonephritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9032",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005342",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005342",
    "nando_id": "NANDO:1200366"
  },
  {
    "id": "C0877024",
    "id2": "MedGen UID:164078",
    "medgen_label": "Schimke immuno-osseous dysplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/164078",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009458",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009458",
    "nando_id": "NANDO:1200337"
  },
  {
    "id": "C1527336",
    "id2": "MedGen UID:282890",
    "medgen_label": "Sjogren syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/282890",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010030",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010030",
    "nando_id": "NANDO:1200279"
  },
  {
    "id": "C1527336",
    "id2": "MedGen UID:282890",
    "medgen_label": "Sjogren syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/282890",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0010030",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010030",
    "nando_id": "NANDO:1200280"
  },
  {
    "id": "C4049006",
    "id2": "MedGen UID:883982",
    "medgen_label": "Selective IgA deficiency disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/883982",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001341",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001341",
    "nando_id": "NANDO:1200347"
  },
  {
    "id": "C5681331",
    "id2": "MedGen UID:1826154",
    "medgen_label": "Inherited aplastic anemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1826154",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001713",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001713",
    "nando_id": "NANDO:1200302"
  },
  {
    "id": "C1853118",
    "id2": "MedGen UID:343974",
    "medgen_label": "Severe congenital neutropenia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/343974",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018542",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018542",
    "nando_id": "NANDO:1200353"
  },
  {
    "id": "C0002874",
    "id2": "MedGen UID:8063",
    "medgen_label": "Aplastic anemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/8063",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015909",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015909",
    "nando_id": "NANDO:1200295"
  },
  {
    "id": "C0002874",
    "id2": "MedGen UID:8063",
    "medgen_label": "Aplastic anemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/8063",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0015909",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015909",
    "nando_id": "NANDO:1200301"
  },
  {
    "id": "C0002880",
    "id2": "MedGen UID:1918",
    "medgen_label": "Autoimmune hemolytic anemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1918",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020108",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020108",
    "nando_id": "NANDO:1200305"
  },
  {
    "id": "C0006845",
    "id2": "MedGen UID:2426",
    "medgen_label": "Chronic mucocutaneous candidiasis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/2426",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015279",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015279",
    "nando_id": "NANDO:1200363"
  },
  {
    "id": "C0009447",
    "id2": "MedGen UID:40407",
    "medgen_label": "Common variable immunodeficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/40407",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015517",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015517",
    "nando_id": "NANDO:1200344"
  },
  {
    "id": "C0011633",
    "id2": "MedGen UID:8331",
    "medgen_label": "Dermatomyositis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/8331",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016367",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016367",
    "nando_id": "NANDO:1200274"
  },
  {
    "id": "C0406645",
    "id2": "MedGen UID:96065",
    "medgen_label": "Amyopathic dermatomyositis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/96065",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0043317",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0043317",
    "nando_id": "NANDO:1200275"
  },
  {
    "id": "C2584778",
    "id2": "MedGen UID:391723",
    "medgen_label": "Acquired thrombotic thrombocytopenic purpura",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/391723",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019740",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019740",
    "nando_id": "NANDO:1200318"
  },
  {
    "id": "C2584778",
    "id2": "MedGen UID:391723",
    "medgen_label": "Acquired thrombotic thrombocytopenic purpura",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/391723",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0019740",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019740",
    "nando_id": "NANDO:1200319"
  },
  {
    "id": "C2677092",
    "id2": "MedGen UID:383023",
    "medgen_label": "Pyogenic bacterial infections due to MyD88 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/383023",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012839",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012839",
    "nando_id": "NANDO:1200362"
  },
  {
    "id": "C2677792",
    "id2": "MedGen UID:394368",
    "medgen_label": "RIDDLE syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/394368",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012764",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012764",
    "nando_id": "NANDO:1200336"
  },
  {
    "id": "C5234937",
    "id2": "MedGen UID:1720114",
    "medgen_label": "Decreased circulating IgG concentration",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1720114",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0045045",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0045045",
    "nando_id": "NANDO:1200346"
  },
  {
    "id": "C0265965",
    "id2": "MedGen UID:78580",
    "medgen_label": "Dyskeratosis congenita",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78580",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015780",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015780",
    "nando_id": "NANDO:1200304"
  },
  {
    "id": "C0268125",
    "id2": "MedGen UID:75653",
    "medgen_label": "Purine-nucleoside phosphorylase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75653",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013171",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013171",
    "nando_id": "NANDO:1200325"
  },
  {
    "id": "C0348890",
    "id2": "MedGen UID:87595",
    "medgen_label": "Idiopathic aplastic anemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/87595",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012197",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012197",
    "nando_id": "NANDO:1200296"
  },
  {
    "id": "C1264008",
    "id2": "MedGen UID:688249",
    "medgen_label": "Cold agglutinin disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/688249",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018922",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018922",
    "nando_id": "NANDO:1200307"
  },
  {
    "id": "C3266863",
    "id2": "MedGen UID:473805",
    "medgen_label": "Inherited susceptibility to mycobacterial diseases",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/473805",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019146",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019146",
    "nando_id": "NANDO:1200359"
  },
  {
    "id": "C3808553",
    "id2": "MedGen UID:814883",
    "medgen_label": "Autosomal dominant aplasia and myelodysplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/814883",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0013851",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013851",
    "nando_id": "NANDO:1200301"
  },
  {
    "id": "C0085253",
    "id2": "MedGen UID:39007",
    "medgen_label": "Adult-onset Still disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/39007",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019355",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019355",
    "nando_id": "NANDO:1200282"
  },
  {
    "id": "C0085655",
    "id2": "MedGen UID:39086",
    "medgen_label": "Polymyositis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/39086",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019127",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019127",
    "nando_id": "NANDO:1200276"
  },
  {
    "id": "C0086774",
    "id2": "MedGen UID:39693",
    "medgen_label": "Paroxysmal cold hemoglobinuria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/39693",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019533",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019533",
    "nando_id": "NANDO:1200308"
  },
  {
    "id": "C1837065",
    "id2": "MedGen UID:323058",
    "medgen_label": "Susceptibility to respiratory infections associated with CD8alpha chain mutation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/323058",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012161",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012161",
    "nando_id": "NANDO:1200326"
  },
  {
    "id": "C1843256",
    "id2": "MedGen UID:375137",
    "medgen_label": "Immunodeficiency 67",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/375137",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011888",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011888",
    "nando_id": "NANDO:1200361"
  },
  {
    "id": "C3887645",
    "id2": "MedGen UID:854488",
    "medgen_label": "Hyper-IgE syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/854488",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018037",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018037",
    "nando_id": "NANDO:1200340"
  },
  {
    "id": "C0032453",
    "id2": "MedGen UID:45995",
    "medgen_label": "Relapsing polychondritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/45995",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019125",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019125",
    "nando_id": "NANDO:1200283"
  },
  {
    "id": "C0034155",
    "id2": "MedGen UID:48266",
    "medgen_label": "Thrombotic thrombocytopenic purpura",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/48266",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018896",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018896",
    "nando_id": "NANDO:1200316"
  },
  {
    "id": "C0272118",
    "id2": "MedGen UID:450541",
    "medgen_label": "Autoimmune hemolytic anemia, warm type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/450541",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019532",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019532",
    "nando_id": "NANDO:1200306"
  },
  {
    "id": "C0272126",
    "id2": "MedGen UID:75773",
    "medgen_label": "Evans syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75773",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016030",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016030",
    "nando_id": "NANDO:1200310"
  },
  {
    "id": "C0272187",
    "id2": "MedGen UID:124419",
    "medgen_label": "Leukocyte adhesion deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/124419",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017570",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017570",
    "nando_id": "NANDO:1200355"
  },
  {
    "id": "C0272238",
    "id2": "MedGen UID:124421",
    "medgen_label": "Transient hypogammaglobulinemia of infancy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/124421",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015698",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015698",
    "nando_id": "NANDO:1200349"
  },
  {
    "id": "C4305257",
    "id2": "MedGen UID:930926",
    "medgen_label": "Mixed-type autoimmune hemolytic anemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/930926",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019534",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019534",
    "nando_id": "NANDO:1200309"
  },
  {
    "id": "C0018203",
    "id2": "MedGen UID:5377",
    "medgen_label": "Chronic granulomatous disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5377",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018305",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018305",
    "nando_id": "NANDO:1200357"
  },
  {
    "id": "C0019243",
    "id2": "MedGen UID:9229",
    "medgen_label": "Hereditary angioneurotic edema",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9229",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019623",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019623",
    "nando_id": "NANDO:1200365"
  },
  {
    "id": "C5680885",
    "id2": "MedGen UID:1843079",
    "medgen_label": "Non-familial restrictive cardiomyopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1843079",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016345",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016345",
    "nando_id": "NANDO:1200294"
  },
  {
    "id": "CN294181",
    "id2": "MedGen UID:977689",
    "medgen_label": "22q11.2 deletion syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/977689",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018923",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018923",
    "nando_id": "NANDO:1200339"
  },
  {
    "id": "CN301239",
    "id2": "MedGen UID:985772",
    "medgen_label": "Autoimmune lymphoproliferative syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/985772",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017979",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017979",
    "nando_id": "NANDO:1200352"
  },
  {
    "id": "C1848296",
    "id2": "MedGen UID:341190",
    "medgen_label": "46,XY sex reversal 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/341190",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010226",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010226",
    "nando_id": "NANDO:1200404"
  },
  {
    "id": "C0001403",
    "id2": "MedGen UID:1324",
    "medgen_label": "Primary adrenocortical insufficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1324",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015129",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015129",
    "nando_id": "NANDO:1200411"
  },
  {
    "id": "C0001627",
    "id2": "MedGen UID:7900",
    "medgen_label": "Congenital adrenal hyperplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7900",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018479",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018479",
    "nando_id": "NANDO:1200396"
  },
  {
    "id": "C0001627",
    "id2": "MedGen UID:7900",
    "medgen_label": "Congenital adrenal hyperplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7900",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018479",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018479",
    "nando_id": "NANDO:1200397"
  },
  {
    "id": "C0008312",
    "id2": "MedGen UID:3035",
    "medgen_label": "Primary biliary cholangitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/3035",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005388",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005388",
    "nando_id": "NANDO:1200439"
  },
  {
    "id": "C0008313",
    "id2": "MedGen UID:3036",
    "medgen_label": "Sclerosing cholangitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/3036",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018646",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018646",
    "nando_id": "NANDO:1200440"
  },
  {
    "id": "C0009324",
    "id2": "MedGen UID:3532",
    "medgen_label": "Ulcerative colitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/3532",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005101",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005101",
    "nando_id": "NANDO:1200449"
  },
  {
    "id": "C0010346",
    "id2": "MedGen UID:3664",
    "medgen_label": "Crohn disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/3664",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005011",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005011",
    "nando_id": "NANDO:1200444"
  },
  {
    "id": "C0010346",
    "id2": "MedGen UID:3664",
    "medgen_label": "Crohn disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/3664",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0005011",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005011",
    "nando_id": "NANDO:1200446"
  },
  {
    "id": "C0156146",
    "id2": "MedGen UID:57617",
    "medgen_label": "Small bowel Crohn disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/57617",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005539",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005539",
    "nando_id": "NANDO:1200445"
  },
  {
    "id": "C0156147",
    "id2": "MedGen UID:57618",
    "medgen_label": "Crohn disease of large bowel",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/57618",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005532",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005532",
    "nando_id": "NANDO:1200446"
  },
  {
    "id": "C0221406",
    "id2": "MedGen UID:66381",
    "medgen_label": "Pituitary dependent hypercortisolism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/66381",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009050",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009050",
    "nando_id": "NANDO:1200379"
  },
  {
    "id": "C2350236",
    "id2": "MedGen UID:389939",
    "medgen_label": "Idiopathic interstitial pneumonia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/389939",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002429",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002429",
    "nando_id": "NANDO:1200416"
  },
  {
    "id": "C2936858",
    "id2": "MedGen UID:424833",
    "medgen_label": "Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/424833",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008728",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008728",
    "nando_id": "NANDO:1200399"
  },
  {
    "id": "C2940786",
    "id2": "MedGen UID:424854",
    "medgen_label": "Thyroid hormone resistance syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/424854",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001328",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001328",
    "nando_id": "NANDO:1200395"
  },
  {
    "id": "C2973725",
    "id2": "MedGen UID:425404",
    "medgen_label": "Pulmonary arterial hypertension",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/425404",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015924",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015924",
    "nando_id": "NANDO:1200425"
  },
  {
    "id": "C0022680",
    "id2": "MedGen UID:9639",
    "medgen_label": "Polycystic kidney disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9639",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020642",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020642",
    "nando_id": "NANDO:1200367"
  },
  {
    "id": "C0268285",
    "id2": "MedGen UID:82782",
    "medgen_label": "Deficiency of steroid 17-alpha-monooxygenase",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82782",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008730",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008730",
    "nando_id": "NANDO:1200401"
  },
  {
    "id": "C0268292",
    "id2": "MedGen UID:82783",
    "medgen_label": "Deficiency of steroid 11-beta-monooxygenase",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82783",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008729",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008729",
    "nando_id": "NANDO:1200400"
  },
  {
    "id": "C0346303",
    "id2": "MedGen UID:87550",
    "medgen_label": "TSH-secreting pituitary adenoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/87550",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019611",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019611",
    "nando_id": "NANDO:1200377"
  },
  {
    "id": "C0949272",
    "id2": "MedGen UID:184943",
    "medgen_label": "Ileocolitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/184943",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005534",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005534",
    "nando_id": "NANDO:1200447"
  },
  {
    "id": "C1262481",
    "id2": "MedGen UID:220382",
    "medgen_label": "Eosinophilic gastroenteritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/220382",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016129",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016129",
    "nando_id": "NANDO:1200457"
  },
  {
    "id": "C1279945",
    "id2": "MedGen UID:224822",
    "medgen_label": "Acute interstitial pneumonia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/224822",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019203",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019203",
    "nando_id": "NANDO:1200420"
  },
  {
    "id": "C1860042",
    "id2": "MedGen UID:348008",
    "medgen_label": "Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/348008",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013310",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013310",
    "nando_id": "NANDO:1200402"
  },
  {
    "id": "C1861329",
    "id2": "MedGen UID:396107",
    "medgen_label": "Spinal canal stenosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/396107",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005965",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005965",
    "nando_id": "NANDO:1200372"
  },
  {
    "id": "C3489793",
    "id2": "MedGen UID:483746",
    "medgen_label": "46,XY sex reversal 3",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/483746",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013066",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013066",
    "nando_id": "NANDO:1200405"
  },
  {
    "id": "C3489796",
    "id2": "MedGen UID:483749",
    "medgen_label": "Thyroid hormone resistance, generalized, autosomal recessive",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/483749",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0010131",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010131",
    "nando_id": "NANDO:1200395"
  },
  {
    "id": "C3698354",
    "id2": "MedGen UID:785618",
    "medgen_label": "Pulmonary veno-occlusive disease and/or pulmonary capillary haemangiomatosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/785618",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018554",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018554",
    "nando_id": "NANDO:1200426"
  },
  {
    "id": "C3698354",
    "id2": "MedGen UID:785618",
    "medgen_label": "Pulmonary veno-occlusive disease and/or pulmonary capillary haemangiomatosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/785618",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018554",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018554",
    "nando_id": "NANDO:1200428"
  },
  {
    "id": "C4275066",
    "id2": "MedGen UID:909851",
    "medgen_label": "Familial avascular necrosis of the femoral head",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/909851",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012126",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012126",
    "nando_id": "NANDO:1200373"
  },
  {
    "id": "C4302200",
    "id2": "MedGen UID:927869",
    "medgen_label": "Congenital central hypothyroidism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/927869",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016410",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016410",
    "nando_id": "NANDO:1200390"
  },
  {
    "id": "C4721555",
    "id2": "MedGen UID:1666753",
    "medgen_label": "Autoimmune hepatitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1666753",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016264",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016264",
    "nando_id": "NANDO:1200441"
  },
  {
    "id": "C4721555",
    "id2": "MedGen UID:1666753",
    "medgen_label": "Autoimmune hepatitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1666753",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0016264",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016264",
    "nando_id": "NANDO:1200442"
  },
  {
    "id": "C0085413",
    "id2": "MedGen UID:88404",
    "medgen_label": "Autosomal dominant polycystic kidney disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/88404",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0004691",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004691",
    "nando_id": "NANDO:1200368"
  },
  {
    "id": "C0085548",
    "id2": "MedGen UID:39076",
    "medgen_label": "Autosomal recessive polycystic kidney disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/39076",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009889",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009889",
    "nando_id": "NANDO:1200369"
  },
  {
    "id": "C0341106",
    "id2": "MedGen UID:83318",
    "medgen_label": "Eosinophilic esophagitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/83318",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005361",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005361",
    "nando_id": "NANDO:1200456"
  },
  {
    "id": "C0342394",
    "id2": "MedGen UID:574999",
    "medgen_label": "Neurohypophyseal diabetes insipidus",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/574999",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007450",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007450",
    "nando_id": "NANDO:1200375"
  },
  {
    "id": "C0342471",
    "id2": "MedGen UID:452446",
    "medgen_label": "3 beta-Hydroxysteroid dehydrogenase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/452446",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008727",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008727",
    "nando_id": "NANDO:1200398"
  },
  {
    "id": "C0342482",
    "id2": "MedGen UID:87442",
    "medgen_label": "Congenital adrenal hypoplasia, X-linked",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/87442",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0010264",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010264",
    "nando_id": "NANDO:1200403"
  },
  {
    "id": "C0342543",
    "id2": "MedGen UID:90985",
    "medgen_label": "Central precocious puberty",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/90985",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019165",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019165",
    "nando_id": "NANDO:1200381"
  },
  {
    "id": "C0342881",
    "id2": "MedGen UID:575266",
    "medgen_label": "Homozygous familial hypercholesterolemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/575266",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018328",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018328",
    "nando_id": "NANDO:1200394"
  },
  {
    "id": "C0345240",
    "id2": "MedGen UID:83378",
    "medgen_label": "Aganglionosis, total intestinal",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/83378",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008738",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008738",
    "nando_id": "NANDO:1200460"
  },
  {
    "id": "C0687720",
    "id2": "MedGen UID:146919",
    "medgen_label": "Central diabetes insipidus",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/146919",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015790",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015790",
    "nando_id": "NANDO:1200375"
  },
  {
    "id": "C1846009",
    "id2": "MedGen UID:337364",
    "medgen_label": "IMAGe syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/337364",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013873",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013873",
    "nando_id": "NANDO:1200406"
  },
  {
    "id": "C0033375",
    "id2": "MedGen UID:10936",
    "medgen_label": "Prolactin-producing pituitary gland adenoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10936",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010911",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010911",
    "nando_id": "NANDO:1200378"
  },
  {
    "id": "C0034091",
    "id2": "MedGen UID:18769",
    "medgen_label": "Pulmonary venoocclusive disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/18769",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009937",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009937",
    "nando_id": "NANDO:1200427"
  },
  {
    "id": "C0035334",
    "id2": "MedGen UID:20551",
    "medgen_label": "Retinitis pigmentosa",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/20551",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019200",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019200",
    "nando_id": "NANDO:1200431"
  },
  {
    "id": "C0036202",
    "id2": "MedGen UID:48554",
    "medgen_label": "Sarcoidosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/48554",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019338",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019338",
    "nando_id": "NANDO:1200415"
  },
  {
    "id": "C0271623",
    "id2": "MedGen UID:82883",
    "medgen_label": "Hypogonadotropic hypogonadism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82883",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018555",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018555",
    "nando_id": "NANDO:1200388"
  },
  {
    "id": "C0271742",
    "id2": "MedGen UID:82889",
    "medgen_label": "Glucocorticoid deficiency with achalasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82889",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009279",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009279",
    "nando_id": "NANDO:1200410"
  },
  {
    "id": "C0278864",
    "id2": "MedGen UID:82999",
    "medgen_label": "Growth hormone-producing pituitary gland adenoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82999",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0006238",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006238",
    "nando_id": "NANDO:1200386"
  },
  {
    "id": "C0278864",
    "id2": "MedGen UID:82999",
    "medgen_label": "Growth hormone-producing pituitary gland adenoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82999",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0006238",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006238",
    "nando_id": "NANDO:1200385"
  },
  {
    "id": "C1865343",
    "id2": "MedGen UID:355447",
    "medgen_label": "Ossification of the posterior longitudinal ligament of the spine",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/355447",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011230",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011230",
    "nando_id": "NANDO:1200371"
  },
  {
    "id": "C2748504",
    "id2": "MedGen UID:440560",
    "medgen_label": "Chronic thromboembolic pulmonary hypertension",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/440560",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013024",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013024",
    "nando_id": "NANDO:1200429"
  },
  {
    "id": "C0020635",
    "id2": "MedGen UID:9386",
    "medgen_label": "Hypopituitarism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9386",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005152",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005152",
    "nando_id": "NANDO:1200387"
  },
  {
    "id": "C0021141",
    "id2": "MedGen UID:5772",
    "medgen_label": "Inappropriate antidiuretic hormone secretion",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5772",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006802",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006802",
    "nando_id": "NANDO:1200376"
  },
  {
    "id": "C0238062",
    "id2": "MedGen UID:536759",
    "medgen_label": "Chronic intestinal pseudoobstruction",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/536759",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017574",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017574",
    "nando_id": "NANDO:1200458"
  },
  {
    "id": "C0238378",
    "id2": "MedGen UID:65962",
    "medgen_label": "Desquamative interstitial pneumonia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/65962",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009887",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009887",
    "nando_id": "NANDO:1200422"
  },
  {
    "id": "C0238378",
    "id2": "MedGen UID:65962",
    "medgen_label": "Desquamative interstitial pneumonia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/65962",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009887",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009887",
    "nando_id": "NANDO:1200423"
  },
  {
    "id": "C0242770",
    "id2": "MedGen UID:116663",
    "medgen_label": "Bronchiolitis obliterans organizing pneumonia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/116663",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015264",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015264",
    "nando_id": "NANDO:1200421"
  },
  {
    "id": "C0264511",
    "id2": "MedGen UID:82682",
    "medgen_label": "Lymphoid interstitial pneumonia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82682",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009537",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009537",
    "nando_id": "NANDO:1200424"
  },
  {
    "id": "C0566602",
    "id2": "MedGen UID:107565",
    "medgen_label": "Primary sclerosing cholangitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/107565",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013433",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013433",
    "nando_id": "NANDO:1200440"
  },
  {
    "id": "C0751674",
    "id2": "MedGen UID:148366",
    "medgen_label": "Lymphangiomyomatosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/148366",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011705",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011705",
    "nando_id": "NANDO:1200430"
  },
  {
    "id": "C0856761",
    "id2": "MedGen UID:163632",
    "medgen_label": "Budd-Chiari syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/163632",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010947",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010947",
    "nando_id": "NANDO:1200437"
  },
  {
    "id": "C0860168",
    "id2": "MedGen UID:678582",
    "medgen_label": "Distal colitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/678582",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005533",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005533",
    "nando_id": "NANDO:1200451"
  },
  {
    "id": "C0868908",
    "id2": "MedGen UID:1720692",
    "medgen_label": "Pancolitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1720692",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005536",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005536",
    "nando_id": "NANDO:1200450"
  },
  {
    "id": "C1290344",
    "id2": "MedGen UID:220936",
    "medgen_label": "Non-specific interstitial pneumonia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/220936",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019622",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019622",
    "nando_id": "NANDO:1200419"
  },
  {
    "id": "C5680014",
    "id2": "MedGen UID:1826142",
    "medgen_label": "Eosinophilic gastrointestinal disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1826142",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018438",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018438",
    "nando_id": "NANDO:1200454"
  },
  {
    "id": "C1832466",
    "id2": "MedGen UID:318633",
    "medgen_label": "Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/318633",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011038",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011038",
    "nando_id": "NANDO:1200526"
  },
  {
    "id": "C1832855",
    "id2": "MedGen UID:371427",
    "medgen_label": "Dystonia 9",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/371427",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010983",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010983",
    "nando_id": "NANDO:1200520"
  },
  {
    "id": "C1851920",
    "id2": "MedGen UID:342121",
    "medgen_label": "Dystonia 5",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/342121",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0007495",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007495",
    "nando_id": "NANDO:1200516"
  },
  {
    "id": "C1851943",
    "id2": "MedGen UID:342124",
    "medgen_label": "Torsion dystonia 4",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/342124",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007493",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007493",
    "nando_id": "NANDO:1200515"
  },
  {
    "id": "C1851945",
    "id2": "MedGen UID:338823",
    "medgen_label": "Early-onset generalized limb-onset dystonia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/338823",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007492",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007492",
    "nando_id": "NANDO:1200512"
  },
  {
    "id": "C0221055",
    "id2": "MedGen UID:113142",
    "medgen_label": "Paramyotonia congenita of Von Eulenburg",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/113142",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008195",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008195",
    "nando_id": "NANDO:1200501"
  },
  {
    "id": "C0409818",
    "id2": "MedGen UID:98370",
    "medgen_label": "Chronic infantile neurological, cutaneous and articular syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/98370",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011776",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011776",
    "nando_id": "NANDO:1200468"
  },
  {
    "id": "C0410174",
    "id2": "MedGen UID:140820",
    "medgen_label": "Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/140820",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009678",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009678",
    "nando_id": "NANDO:1200494"
  },
  {
    "id": "C1970149",
    "id2": "MedGen UID:370188",
    "medgen_label": "Paroxysmal nonkinesigenic dyskinesia 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/370188",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012629",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012629",
    "nando_id": "NANDO:1200533"
  },
  {
    "id": "C1970238",
    "id2": "MedGen UID:410022",
    "medgen_label": "Episodic kinesigenic dyskinesia 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/410022",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012603",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012603",
    "nando_id": "NANDO:1200532"
  },
  {
    "id": "C2316212",
    "id2": "MedGen UID:412215",
    "medgen_label": "Cryopyrin associated periodic syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/412215",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016168",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016168",
    "nando_id": "NANDO:1200465"
  },
  {
    "id": "C2676281",
    "id2": "MedGen UID:391003",
    "medgen_label": "Torsion dystonia 17",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/391003",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012895",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012895",
    "nando_id": "NANDO:1200530"
  },
  {
    "id": "C2677567",
    "id2": "MedGen UID:436979",
    "medgen_label": "Dystonia 16",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/436979",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012789",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012789",
    "nando_id": "NANDO:1200529"
  },
  {
    "id": "C2931788",
    "id2": "MedGen UID:444141",
    "medgen_label": "Atypical hemolytic-uremic syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/444141",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0016244",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016244",
    "nando_id": "NANDO:1200474"
  },
  {
    "id": "C0024814",
    "id2": "MedGen UID:6222",
    "medgen_label": "Marinesco-Sjögren syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6222",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009567",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009567",
    "nando_id": "NANDO:1200485"
  },
  {
    "id": "C0027126",
    "id2": "MedGen UID:10239",
    "medgen_label": "Myotonic dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10239",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016107",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016107",
    "nando_id": "NANDO:1200495"
  },
  {
    "id": "C0030443",
    "id2": "MedGen UID:18291",
    "medgen_label": "Familial periodic paralysis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/18291",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000995",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000995",
    "nando_id": "NANDO:1200502"
  },
  {
    "id": "C0268390",
    "id2": "MedGen UID:120634",
    "medgen_label": "Familial amyloid nephropathy with urticaria AND deafness",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120634",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008633",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008633",
    "nando_id": "NANDO:1200467"
  },
  {
    "id": "C0270952",
    "id2": "MedGen UID:75730",
    "medgen_label": "Oculopharyngeal muscular dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75730",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008116",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008116",
    "nando_id": "NANDO:1200493"
  },
  {
    "id": "C0546264",
    "id2": "MedGen UID:108177",
    "medgen_label": "Congenital myopathy with fiber type disproportion",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/108177",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009711",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009711",
    "nando_id": "NANDO:1200483"
  },
  {
    "id": "C1275081",
    "id2": "MedGen UID:266149",
    "medgen_label": "Cardio-facio-cutaneous syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/266149",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015280",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015280",
    "nando_id": "NANDO:1200462"
  },
  {
    "id": "C1275126",
    "id2": "MedGen UID:226899",
    "medgen_label": "TNF receptor-associated periodic fever syndrome (TRAPS)",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/226899",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007727",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007727",
    "nando_id": "NANDO:1200472"
  },
  {
    "id": "C1857093",
    "id2": "MedGen UID:346511",
    "medgen_label": "Torsion dystonia 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/346511",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009141",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009141",
    "nando_id": "NANDO:1200513"
  },
  {
    "id": "C3280371",
    "id2": "MedGen UID:482001",
    "medgen_label": "Neurodegeneration with brain iron accumulation 4",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/482001",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013674",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013674",
    "nando_id": "NANDO:1200540"
  },
  {
    "id": "C3495559",
    "id2": "MedGen UID:760659",
    "medgen_label": "Juvenile idiopathic arthritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/760659",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011429",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011429",
    "nando_id": "NANDO:1200469"
  },
  {
    "id": "C3496228",
    "id2": "MedGen UID:501249",
    "medgen_label": "Hereditary spastic paraplegia 35",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/501249",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0012866",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012866",
    "nando_id": "NANDO:1200541"
  },
  {
    "id": "C5201146",
    "id2": "MedGen UID:1684759",
    "medgen_label": "Blau syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1684759",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008523",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008523",
    "nando_id": "NANDO:1200476"
  },
  {
    "id": "C0338488",
    "id2": "MedGen UID:90925",
    "medgen_label": "Alternating hemiplegia of childhood",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/90925",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016241",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016241",
    "nando_id": "NANDO:1200525"
  },
  {
    "id": "C0587248",
    "id2": "MedGen UID:108454",
    "medgen_label": "Costello syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/108454",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009026",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009026",
    "nando_id": "NANDO:1200463"
  },
  {
    "id": "C1414216",
    "id2": "MedGen UID:236274",
    "medgen_label": "Torsion dystonia 6",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/236274",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011264",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011264",
    "nando_id": "NANDO:1200517"
  },
  {
    "id": "C1838577",
    "id2": "MedGen UID:325051",
    "medgen_label": "CARASIL syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/325051",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010829",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010829",
    "nando_id": "NANDO:1200544"
  },
  {
    "id": "C1839130",
    "id2": "MedGen UID:326820",
    "medgen_label": "X-linked dystonia-parkinsonism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/326820",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010747",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010747",
    "nando_id": "NANDO:1200514"
  },
  {
    "id": "C1842534",
    "id2": "MedGen UID:330866",
    "medgen_label": "Childhood onset GLUT1 deficiency syndrome 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/330866",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012805",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012805",
    "nando_id": "NANDO:1200531"
  },
  {
    "id": "C1843264",
    "id2": "MedGen UID:335918",
    "medgen_label": "Torsion dystonia 13",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/335918",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011886",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011886",
    "nando_id": "NANDO:1200527"
  },
  {
    "id": "C1843786",
    "id2": "MedGen UID:334492",
    "medgen_label": "Myoclonic dystonia 15",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/334492",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011844",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011844",
    "nando_id": "NANDO:1200528"
  },
  {
    "id": "C1865818",
    "id2": "MedGen UID:355560",
    "medgen_label": "Torsion dystonia 7",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/355560",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011200",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011200",
    "nando_id": "NANDO:1200518"
  },
  {
    "id": "C1868681",
    "id2": "MedGen UID:358384",
    "medgen_label": "Dystonia 12",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/358384",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0007496",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007496",
    "nando_id": "NANDO:1200524"
  },
  {
    "id": "C1868681",
    "id2": "MedGen UID:358384",
    "medgen_label": "Dystonia 12",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/358384",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007496",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007496",
    "nando_id": "NANDO:1200523"
  },
  {
    "id": "C0013264",
    "id2": "MedGen UID:3925",
    "medgen_label": "Duchenne muscular dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/3925",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010679",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010679",
    "nando_id": "NANDO:1200488"
  },
  {
    "id": "C0018523",
    "id2": "MedGen UID:6708",
    "medgen_label": "Pigmentary pallidal degeneration",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6708",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009319",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009319",
    "nando_id": "NANDO:1200534"
  },
  {
    "id": "C0238288",
    "id2": "MedGen UID:65956",
    "medgen_label": "Facioscapulohumeral muscular dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/65956",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001347",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001347",
    "nando_id": "NANDO:1200491"
  },
  {
    "id": "C0238357",
    "id2": "MedGen UID:68665",
    "medgen_label": "Familial hyperkalemic periodic paralysis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/68665",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008224",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008224",
    "nando_id": "NANDO:1200504"
  },
  {
    "id": "C0238358",
    "id2": "MedGen UID:116058",
    "medgen_label": "Hypokalemic periodic paralysis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/116058",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008223",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008223",
    "nando_id": "NANDO:1200503"
  },
  {
    "id": "C0265354",
    "id2": "MedGen UID:75567",
    "medgen_label": "CHARGE syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75567",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008965",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008965",
    "nando_id": "NANDO:1200464"
  },
  {
    "id": "C0751360",
    "id2": "MedGen UID:155852",
    "medgen_label": "Congenital myotonia, autosomal recessive form",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155852",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009715",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009715",
    "nando_id": "NANDO:1200499"
  },
  {
    "id": "C0751587",
    "id2": "MedGen UID:199687",
    "medgen_label": "Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/199687",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007432",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007432",
    "nando_id": "NANDO:1200545"
  },
  {
    "id": "C0751951",
    "id2": "MedGen UID:199773",
    "medgen_label": "Central core myopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/199773",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007294",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007294",
    "nando_id": "NANDO:1200479"
  },
  {
    "id": "C0752282",
    "id2": "MedGen UID:156050",
    "medgen_label": "Congenital structural myopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/156050",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0002921",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002921",
    "nando_id": "NANDO:1200482"
  },
  {
    "id": "C0878682",
    "id2": "MedGen UID:168057",
    "medgen_label": "Deficiency of ferroxidase",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/168057",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0011426",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011426",
    "nando_id": "NANDO:1200540"
  },
  {
    "id": "C0917713",
    "id2": "MedGen UID:182959",
    "medgen_label": "Becker muscular dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/182959",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010311",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010311",
    "nando_id": "NANDO:1200489"
  },
  {
    "id": "C5679787",
    "id2": "MedGen UID:1826053",
    "medgen_label": "Qualitative or quantitative defects of dystrophin",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1826053",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016147",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016147",
    "nando_id": "NANDO:1200487"
  },
  {
    "id": "CN295306",
    "id2": "MedGen UID:977133",
    "medgen_label": "Myoclonus-dystonia syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/977133",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000903",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000903",
    "nando_id": "NANDO:1200522"
  },
  {
    "id": "CN311573",
    "id2": "MedGen UID:992104",
    "medgen_label": "Thomsen and Becker disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/992104",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009710",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009710",
    "nando_id": "NANDO:1200497"
  },
  {
    "id": "CN311573",
    "id2": "MedGen UID:992104",
    "medgen_label": "Thomsen and Becker disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/992104",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009710",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009710",
    "nando_id": "NANDO:1200498"
  },
  {
    "id": "C0175709",
    "id2": "MedGen UID:104495",
    "medgen_label": "Centronuclear myopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/104495",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018947",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018947",
    "nando_id": "NANDO:1200481"
  },
  {
    "id": "C0175709",
    "id2": "MedGen UID:104495",
    "medgen_label": "Centronuclear myopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/104495",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018947",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018947",
    "nando_id": "NANDO:1200482"
  },
  {
    "id": "C0206157",
    "id2": "MedGen UID:61528",
    "medgen_label": "Nemaline myopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/61528",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018958",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018958",
    "nando_id": "NANDO:1200478"
  },
  {
    "id": "C0410189",
    "id2": "MedGen UID:96078",
    "medgen_label": "Emery-Dreifuss muscular dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/96078",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016830",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016830",
    "nando_id": "NANDO:1200492"
  },
  {
    "id": "C2931788",
    "id2": "MedGen UID:444141",
    "medgen_label": "Atypical hemolytic-uremic syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/444141",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016244",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016244",
    "nando_id": "NANDO:1200473"
  },
  {
    "id": "C2931826",
    "id2": "MedGen UID:444151",
    "medgen_label": "Potassium-aggravated myotonia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/444151",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018959",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018959",
    "nando_id": "NANDO:1200500"
  },
  {
    "id": "C2931845",
    "id2": "MedGen UID:444156",
    "medgen_label": "Neurodegeneration with brain iron accumulation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/444156",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018307",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018307",
    "nando_id": "NANDO:1200542"
  },
  {
    "id": "C2931845",
    "id2": "MedGen UID:444156",
    "medgen_label": "Neurodegeneration with brain iron accumulation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/444156",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018307",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018307",
    "nando_id": "NANDO:1200539"
  },
  {
    "id": "C2938918",
    "id2": "MedGen UID:1371500",
    "medgen_label": "Superficial siderosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1371500",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016594",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016594",
    "nando_id": "NANDO:1200543"
  },
  {
    "id": "C0025312",
    "id2": "MedGen UID:7538",
    "medgen_label": "Myelomeningocele",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7538",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019773",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019773",
    "nando_id": "NANDO:1200509"
  },
  {
    "id": "C0026850",
    "id2": "MedGen UID:44527",
    "medgen_label": "Muscular dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44527",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020121",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020121",
    "nando_id": "NANDO:1200486"
  },
  {
    "id": "C0270724",
    "id2": "MedGen UID:82852",
    "medgen_label": "Infantile neuroaxonal dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82852",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0024457",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0024457",
    "nando_id": "NANDO:1200537"
  },
  {
    "id": "C0270960",
    "id2": "MedGen UID:124381",
    "medgen_label": "Congenital myopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/124381",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019952",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019952",
    "nando_id": "NANDO:1200477"
  },
  {
    "id": "C0270962",
    "id2": "MedGen UID:75731",
    "medgen_label": "Multiminicore myopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75731",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018948",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018948",
    "nando_id": "NANDO:1200480"
  },
  {
    "id": "C1858558",
    "id2": "MedGen UID:346934",
    "medgen_label": "Systemic-onset juvenile idiopathic arthritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/346934",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019434",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019434",
    "nando_id": "NANDO:1200470"
  },
  {
    "id": "C3668943",
    "id2": "MedGen UID:777150",
    "medgen_label": "Fatty acid hydroxylase-associated neurodegeneration",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/777150",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017999",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017999",
    "nando_id": "NANDO:1200541"
  },
  {
    "id": "C0343068",
    "id2": "MedGen UID:137986",
    "medgen_label": "Familial cold autoinflammatory syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/137986",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018768",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018768",
    "nando_id": "NANDO:1200466"
  },
  {
    "id": "C0686353",
    "id2": "MedGen UID:151940",
    "medgen_label": "Limb-girdle muscular dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/151940",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016971",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016971",
    "nando_id": "NANDO:1200490"
  },
  {
    "id": "C5568621",
    "id2": "MedGen UID:1800044",
    "medgen_label": "Atypical pantothenate kinase-associated neurodegeneration",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1800044",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016305",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016305",
    "nando_id": "NANDO:1200536"
  },
  {
    "id": "C0035934",
    "id2": "MedGen UID:48517",
    "medgen_label": "Rubinstein-Taybi syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/48517",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019188",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019188",
    "nando_id": "NANDO:1200461"
  },
  {
    "id": "C0037917",
    "id2": "MedGen UID:21277",
    "medgen_label": "Spina bifida cystica",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21277",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0017069",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017069",
    "nando_id": "NANDO:1200509"
  },
  {
    "id": "C0039144",
    "id2": "MedGen UID:21449",
    "medgen_label": "Syringomyelia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21449",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017987",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017987",
    "nando_id": "NANDO:1200506"
  },
  {
    "id": "C0039144",
    "id2": "MedGen UID:21449",
    "medgen_label": "Syringomyelia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21449",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0017987",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017987",
    "nando_id": "NANDO:1200507"
  },
  {
    "id": "C2931171",
    "id2": "MedGen UID:443993",
    "medgen_label": "Oligoarticular juvenile idiopathic arthritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/443993",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019433",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019433",
    "nando_id": "NANDO:1200471"
  },
  {
    "id": "C0242287",
    "id2": "MedGen UID:116151",
    "medgen_label": "Isaac syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/116151",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019399",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019399",
    "nando_id": "NANDO:1200510"
  },
  {
    "id": "C5679812",
    "id2": "MedGen UID:1826057",
    "medgen_label": "Classic pantothenate kinase-associated neurodegeneration",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1826057",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016304",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016304",
    "nando_id": "NANDO:1200535"
  },
  {
    "id": "C5680022",
    "id2": "MedGen UID:1842468",
    "medgen_label": "Inherited dystonia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1842468",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0044807",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0044807",
    "nando_id": "NANDO:1200511"
  },
  {
    "id": "CN221588",
    "id2": "MedGen UID:808180",
    "medgen_label": "Dopa-responsive dystonia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/808180",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016812",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016812",
    "nando_id": "NANDO:1200516"
  },
  {
    "id": "C1846386",
    "id2": "MedGen UID:375876",
    "medgen_label": "Isolated focal cortical dysplasia type IIa",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/375876",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017101",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017101",
    "nando_id": "NANDO:1200568"
  },
  {
    "id": "C1848137",
    "id2": "MedGen UID:338393",
    "medgen_label": "Developmental and epileptic encephalopathy, 9",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/338393",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010246",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010246",
    "nando_id": "NANDO:1200599"
  },
  {
    "id": "C1848412",
    "id2": "MedGen UID:336339",
    "medgen_label": "Photosensitive trichothiodystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/336339",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002470",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002470",
    "nando_id": "NANDO:1200626"
  },
  {
    "id": "C0175713",
    "id2": "MedGen UID:61236",
    "medgen_label": "Aicardi syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/61236",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010568",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010568",
    "nando_id": "NANDO:1200562"
  },
  {
    "id": "C0205711",
    "id2": "MedGen UID:61440",
    "medgen_label": "Pelizaeus-Merzbacher disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/61440",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010714",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010714",
    "nando_id": "NANDO:1200576"
  },
  {
    "id": "C0221060",
    "id2": "MedGen UID:66357",
    "medgen_label": "Oromandibular-limb hypogenesis spectrum",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/66357",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008006",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008006",
    "nando_id": "NANDO:1200559"
  },
  {
    "id": "C0406344",
    "id2": "MedGen UID:98025",
    "medgen_label": "Follicular ichthyosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/98025",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0043094",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0043094",
    "nando_id": "NANDO:1200628"
  },
  {
    "id": "C0431391",
    "id2": "MedGen UID:140910",
    "medgen_label": "Hemimegalencephaly",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/140910",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020492",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020492",
    "nando_id": "NANDO:1200563"
  },
  {
    "id": "C2676243",
    "id2": "MedGen UID:390993",
    "medgen_label": "Leukoencephalopathy-ataxia-hypodontia-hypomyelination syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/390993",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011897",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011897",
    "nando_id": "NANDO:1200585"
  },
  {
    "id": "C2676244",
    "id2": "MedGen UID:436642",
    "medgen_label": "Hypomyelinating leukodystrophy 6",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/436642",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012905",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012905",
    "nando_id": "NANDO:1200578"
  },
  {
    "id": "C2677109",
    "id2": "MedGen UID:383026",
    "medgen_label": "Hypomyelinating leukodystrophy 4",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/383026",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012824",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012824",
    "nando_id": "NANDO:1200581"
  },
  {
    "id": "C5848247",
    "id2": "MedGen UID:1852191",
    "medgen_label": "Lamellar ichthyosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1852191",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017778",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017778",
    "nando_id": "NANDO:1200617"
  },
  {
    "id": "C0023520",
    "id2": "MedGen UID:6070",
    "medgen_label": "Leukodystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6070",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019046",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019046",
    "nando_id": "NANDO:1200575"
  },
  {
    "id": "C0030804",
    "id2": "MedGen UID:10619",
    "medgen_label": "Mucous membrane pemphigoid",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10619",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018746",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018746",
    "nando_id": "NANDO:1200634"
  },
  {
    "id": "C0030805",
    "id2": "MedGen UID:10620",
    "medgen_label": "Bullous pemphigoid",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10620",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019082",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019082",
    "nando_id": "NANDO:1200633"
  },
  {
    "id": "C0030805",
    "id2": "MedGen UID:10620",
    "medgen_label": "Bullous pemphigoid",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10620",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0019082",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019082",
    "nando_id": "NANDO:1200632"
  },
  {
    "id": "C0266463",
    "id2": "MedGen UID:78604",
    "medgen_label": "Lissencephaly",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78604",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018838",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018838",
    "nando_id": "NANDO:1200574"
  },
  {
    "id": "C0268238",
    "id2": "MedGen UID:82780",
    "medgen_label": "Triglyceride storage disease with ichthyosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82780",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010155",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010155",
    "nando_id": "NANDO:1200622"
  },
  {
    "id": "C0268238",
    "id2": "MedGen UID:82780",
    "medgen_label": "Triglyceride storage disease with ichthyosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82780",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0010155",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010155",
    "nando_id": "NANDO:1200623"
  },
  {
    "id": "C0270726",
    "id2": "MedGen UID:78724",
    "medgen_label": "Alexander disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78724",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008752",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008752",
    "nando_id": "NANDO:1200554"
  },
  {
    "id": "C0393703",
    "id2": "MedGen UID:140741",
    "medgen_label": "Epilepsy with myoclonic absences",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/140741",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019487",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019487",
    "nando_id": "NANDO:1200589"
  },
  {
    "id": "C0393706",
    "id2": "MedGen UID:97959",
    "medgen_label": "Early infantile epileptic encephalopathy with suppression bursts",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/97959",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0100062",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0100062",
    "nando_id": "NANDO:1200593"
  },
  {
    "id": "C0432306",
    "id2": "MedGen UID:98153",
    "medgen_label": "Ichthyosis bullosa of Siemens",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/98153",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007813",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007813",
    "nando_id": "NANDO:1200613"
  },
  {
    "id": "C0432443",
    "id2": "MedGen UID:96605",
    "medgen_label": "Deletion of long arm of chromosome 18",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/96605",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011147",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011147",
    "nando_id": "NANDO:1200579"
  },
  {
    "id": "C0549118",
    "id2": "MedGen UID:639806",
    "medgen_label": "Idiopathic hemiconvulsion-hemiplegia syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/639806",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019485",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019485",
    "nando_id": "NANDO:1200596"
  },
  {
    "id": "C1096903",
    "id2": "MedGen UID:203368",
    "medgen_label": "Salla disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/203368",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011449",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011449",
    "nando_id": "NANDO:1200582"
  },
  {
    "id": "C1274215",
    "id2": "MedGen UID:697564",
    "medgen_label": "Autosomal recessive congenital ichthyosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/697564",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017265",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017265",
    "nando_id": "NANDO:1200615"
  },
  {
    "id": "C3494976",
    "id2": "MedGen UID:782160",
    "medgen_label": "Malignant migrating partial seizures of infancy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/782160",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017385",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017385",
    "nando_id": "NANDO:1200595"
  },
  {
    "id": "C3665333",
    "id2": "MedGen UID:777082",
    "medgen_label": "Keratitis ichthyosis and deafness syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/777082",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018781",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018781",
    "nando_id": "NANDO:1200621"
  },
  {
    "id": "C4274084",
    "id2": "MedGen UID:894734",
    "medgen_label": "Pelizaeus Merzbacher like disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/894734",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017226",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017226",
    "nando_id": "NANDO:1200577"
  },
  {
    "id": "C4707658",
    "id2": "MedGen UID:1645136",
    "medgen_label": "Acute encephalopathy with biphasic seizures and late reduced diffusion",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1645136",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018198",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018198",
    "nando_id": "NANDO:1200552"
  },
  {
    "id": "C4707795",
    "id2": "MedGen UID:1645432",
    "medgen_label": "Isolated focal cortical dysplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1645432",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019009",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019009",
    "nando_id": "NANDO:1200564"
  },
  {
    "id": "C4749367",
    "id2": "MedGen UID:1659013",
    "medgen_label": "Mesial temporal lobe epilepsy with hippocampal sclerosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1659013",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020476",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020476",
    "nando_id": "NANDO:1200588"
  },
  {
    "id": "C0079154",
    "id2": "MedGen UID:38180",
    "medgen_label": "Congenital nonbullous ichthyosiform erythroderma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/38180",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019306",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019306",
    "nando_id": "NANDO:1200616"
  },
  {
    "id": "C0079154",
    "id2": "MedGen UID:38180",
    "medgen_label": "Congenital nonbullous ichthyosiform erythroderma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/38180",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0019306",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019306",
    "nando_id": "NANDO:1200617"
  },
  {
    "id": "C0079588",
    "id2": "MedGen UID:86937",
    "medgen_label": "X-linked ichthyosis with steryl-sulfatase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/86937",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010622",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010622",
    "nando_id": "NANDO:1200625"
  },
  {
    "id": "C0085106",
    "id2": "MedGen UID:43100",
    "medgen_label": "Familial benign pemphigus",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/43100",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008218",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008218",
    "nando_id": "NANDO:1200631"
  },
  {
    "id": "C0338451",
    "id2": "MedGen UID:83266",
    "medgen_label": "Frontotemporal dementia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/83266",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017276",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017276",
    "nando_id": "NANDO:1200548"
  },
  {
    "id": "C0338462",
    "id2": "MedGen UID:83268",
    "medgen_label": "Semantic dementia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/83268",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010857",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010857",
    "nando_id": "NANDO:1200550"
  },
  {
    "id": "C0338503",
    "id2": "MedGen UID:90926",
    "medgen_label": "Septo-optic dysplasia sequence",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/90926",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0008428",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008428",
    "nando_id": "NANDO:1200560"
  },
  {
    "id": "C0598226",
    "id2": "MedGen UID:108615",
    "medgen_label": "Autosomal recessive congenital ichthyosis 4B",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/108615",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009443",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009443",
    "nando_id": "NANDO:1200614"
  },
  {
    "id": "C1836727",
    "id2": "MedGen UID:373160",
    "medgen_label": "PCWH syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/373160",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012198",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012198",
    "nando_id": "NANDO:1200586"
  },
  {
    "id": "C4011788",
    "id2": "MedGen UID:860225",
    "medgen_label": "Behavioral variant of frontotemporal dementia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/860225",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017160",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017160",
    "nando_id": "NANDO:1200549"
  },
  {
    "id": "C0035372",
    "id2": "MedGen UID:48441",
    "medgen_label": "Rett syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/48441",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010726",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010726",
    "nando_id": "NANDO:1200603"
  },
  {
    "id": "C0035372",
    "id2": "MedGen UID:48441",
    "medgen_label": "Rett syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/48441",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0010726",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010726",
    "nando_id": "NANDO:1200604"
  },
  {
    "id": "C0037231",
    "id2": "MedGen UID:11443",
    "medgen_label": "Sjögren-Larsson syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/11443",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010031",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010031",
    "nando_id": "NANDO:1200620"
  },
  {
    "id": "C0037769",
    "id2": "MedGen UID:11519",
    "medgen_label": "West syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/11519",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018097",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018097",
    "nando_id": "NANDO:1200592"
  },
  {
    "id": "C0038505",
    "id2": "MedGen UID:21361",
    "medgen_label": "Sturge-Weber syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21361",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008501",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008501",
    "nando_id": "NANDO:1200606"
  },
  {
    "id": "C0041341",
    "id2": "MedGen UID:22518",
    "medgen_label": "Tuberous sclerosis syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/22518",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001734",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001734",
    "nando_id": "NANDO:1200607"
  },
  {
    "id": "C0043346",
    "id2": "MedGen UID:21943",
    "medgen_label": "Xeroderma pigmentosum",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21943",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019600",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019600",
    "nando_id": "NANDO:1200608"
  },
  {
    "id": "C0282102",
    "id2": "MedGen UID:79381",
    "medgen_label": "Chondrodysplasia punctata 2 X-linked dominant",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/79381",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020603",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020603",
    "nando_id": "NANDO:1200630"
  },
  {
    "id": "C0282512",
    "id2": "MedGen UID:79465",
    "medgen_label": "Landau-Kleffner syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/79465",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009509",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009509",
    "nando_id": "NANDO:1200602"
  },
  {
    "id": "C1864663",
    "id2": "MedGen UID:501134",
    "medgen_label": "Hypomyelination and Congenital Cataract",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/501134",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012514",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012514",
    "nando_id": "NANDO:1200584"
  },
  {
    "id": "C1868594",
    "id2": "MedGen UID:357007",
    "medgen_label": "Perry syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/357007",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008201",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008201",
    "nando_id": "NANDO:1200547"
  },
  {
    "id": "C1955934",
    "id2": "MedGen UID:363064",
    "medgen_label": "Trichothiodystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/363064",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018053",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018053",
    "nando_id": "NANDO:1200627"
  },
  {
    "id": "C1960543",
    "id2": "MedGen UID:743311",
    "medgen_label": "Bickerstaff brainstem encephalitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/743311",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019208",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019208",
    "nando_id": "NANDO:1200551"
  },
  {
    "id": "C2748910",
    "id2": "MedGen UID:440664",
    "medgen_label": "Atypical Rett syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/440664",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017746",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017746",
    "nando_id": "NANDO:1200605"
  },
  {
    "id": "C2930868",
    "id2": "MedGen UID:418934",
    "medgen_label": "Rasmussen subacute encephalitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/418934",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016019",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016019",
    "nando_id": "NANDO:1200598"
  },
  {
    "id": "C4511307",
    "id2": "MedGen UID:1393111",
    "medgen_label": "Keratinopathic ichthyosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1393111",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017266",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017266",
    "nando_id": "NANDO:1200610"
  },
  {
    "id": "C4518639",
    "id2": "MedGen UID:1381392",
    "medgen_label": "Epilepsy of infancy with migrating focal seizures",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1381392",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0100025",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0100025",
    "nando_id": "NANDO:1200595"
  },
  {
    "id": "C5437635",
    "id2": "MedGen UID:1725198",
    "medgen_label": "Autosomal recessive epidermolytic ichthyosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1725198",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0044742",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0044742",
    "nando_id": "NANDO:1200612"
  },
  {
    "id": "C0020074",
    "id2": "MedGen UID:6915",
    "medgen_label": "Hereditary insensitivity to pain with anhidrosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6915",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009746",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009746",
    "nando_id": "NANDO:1200553"
  },
  {
    "id": "C0020757",
    "id2": "MedGen UID:7002",
    "medgen_label": "Ichthyosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7002",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019269",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019269",
    "nando_id": "NANDO:1200618"
  },
  {
    "id": "C0238111",
    "id2": "MedGen UID:116044",
    "medgen_label": "Lennox-Gastaut syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/116044",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016532",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016532",
    "nando_id": "NANDO:1200591"
  },
  {
    "id": "C0265482",
    "id2": "MedGen UID:489853",
    "medgen_label": "Ring chromosome 20 syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/489853",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015436",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015436",
    "nando_id": "NANDO:1200597"
  },
  {
    "id": "C0751122",
    "id2": "MedGen UID:148243",
    "medgen_label": "Severe myoclonic epilepsy in infancy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/148243",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0100135",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0100135",
    "nando_id": "NANDO:1200587"
  },
  {
    "id": "C0795889",
    "id2": "MedGen UID:208645",
    "medgen_label": "Allan-Herndon-Dudley syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/208645",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010354",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010354",
    "nando_id": "NANDO:1200580"
  },
  {
    "id": "C0796204",
    "id2": "MedGen UID:163228",
    "medgen_label": "Worster-Drought syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/163228",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008503",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008503",
    "nando_id": "NANDO:1200558"
  },
  {
    "id": "C0856562",
    "id2": "MedGen UID:797407",
    "medgen_label": "Inherited ichthyosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/797407",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015947",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015947",
    "nando_id": "NANDO:1200609"
  },
  {
    "id": "C4049262",
    "id2": "MedGen UID:1381987",
    "medgen_label": "Febrile infection-related epilepsy syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1381987",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015584",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015584",
    "nando_id": "NANDO:1200600"
  },
  {
    "id": "C5679765",
    "id2": "MedGen UID:1842666",
    "medgen_label": "Isolated focal cortical dysplasia type Ib",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1842666",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017097",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017097",
    "nando_id": "NANDO:1200566"
  },
  {
    "id": "C5679767",
    "id2": "MedGen UID:1843115",
    "medgen_label": "Isolated focal cortical dysplasia type Ia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1843115",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017096",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017096",
    "nando_id": "NANDO:1200565"
  },
  {
    "id": "C5679768",
    "id2": "MedGen UID:1842232",
    "medgen_label": "Isolated focal cortical dysplasia type IIb",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1842232",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017102",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017102",
    "nando_id": "NANDO:1200569"
  },
  {
    "id": "C5679914",
    "id2": "MedGen UID:1842714",
    "medgen_label": "Alexander disease type II",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1842714",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018210",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018210",
    "nando_id": "NANDO:1200556"
  },
  {
    "id": "C5679915",
    "id2": "MedGen UID:1842668",
    "medgen_label": "Alexander disease type I",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1842668",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018209",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018209",
    "nando_id": "NANDO:1200555"
  },
  {
    "id": "CN293953",
    "id2": "MedGen UID:978511",
    "medgen_label": "Neutral lipid storage disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/978511",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0015611",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015611",
    "nando_id": "NANDO:1200622"
  },
  {
    "id": "CN377632",
    "id2": "MedGen UID:1052865",
    "medgen_label": "Autosomal dominant epidermolytic ichthyosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1052865",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020702",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020702",
    "nando_id": "NANDO:1200611"
  },
  {
    "id": "C0012236",
    "id2": "MedGen UID:4297",
    "medgen_label": "DiGeorge syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/4297",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0008564",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008564",
    "nando_id": "NANDO:1200688"
  },
  {
    "id": "C0220704",
    "id2": "MedGen UID:65085",
    "medgen_label": "Velocardiofacial syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/65085",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0008644",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008644",
    "nando_id": "NANDO:1200688"
  },
  {
    "id": "C0268342",
    "id2": "MedGen UID:75672",
    "medgen_label": "Ehlers-Danlos syndrome, kyphoscoliotic type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75672",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0016002",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016002",
    "nando_id": "NANDO:1200649"
  },
  {
    "id": "C0398794",
    "id2": "MedGen UID:585090",
    "medgen_label": "Griscelli syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/585090",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018306",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018306",
    "nando_id": "NANDO:1200640"
  },
  {
    "id": "C0403416",
    "id2": "MedGen UID:96040",
    "medgen_label": "Crescentic glomerulonephritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/96040",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0001645",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001645",
    "nando_id": "NANDO:1200714"
  },
  {
    "id": "C4273131",
    "id2": "MedGen UID:1636666",
    "medgen_label": "Branchiootic syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1636666",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018878",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018878",
    "nando_id": "NANDO:1200675"
  },
  {
    "id": "C0079293",
    "id2": "MedGen UID:37178",
    "medgen_label": "Acquired epidermolysis bullosa",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/37178",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018747",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018747",
    "nando_id": "NANDO:1200635"
  },
  {
    "id": "C0079504",
    "id2": "MedGen UID:36313",
    "medgen_label": "Hermansky-Pudlak syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/36313",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019312",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019312",
    "nando_id": "NANDO:1200638"
  },
  {
    "id": "C0344616",
    "id2": "MedGen UID:87489",
    "medgen_label": "Congenitally corrected transposition of the great arteries",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/87489",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0016301",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016301",
    "nando_id": "NANDO:1200701"
  },
  {
    "id": "C1839780",
    "id2": "MedGen UID:333403",
    "medgen_label": "Fragile X-associated tremor/ataxia syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/333403",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0010382",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010382",
    "nando_id": "NANDO:1200690"
  },
  {
    "id": "C0078918",
    "id2": "MedGen UID:36250",
    "medgen_label": "Oculocutaneous albinism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/36250",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018910",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018910",
    "nando_id": "NANDO:1200637"
  },
  {
    "id": "C0078918",
    "id2": "MedGen UID:36250",
    "medgen_label": "Oculocutaneous albinism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/36250",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018910",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018910",
    "nando_id": "NANDO:1200641"
  },
  {
    "id": "C0021345",
    "id2": "MedGen UID:7069",
    "medgen_label": "Infectious mononucleosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7069",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0005810",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005810",
    "nando_id": "NANDO:1200668"
  },
  {
    "id": "C5679811",
    "id2": "MedGen UID:1843053",
    "medgen_label": "Congenitally uncorrected transposition of the great arteries with cardiac malformation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1843053",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0016303",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016303",
    "nando_id": "NANDO:1200701"
  },
  {
    "id": "C1567741",
    "id2": "MedGen UID:339209",
    "medgen_label": "Alport syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/339209",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018965",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018965",
    "nando_id": "NANDO:1200712"
  },
  {
    "id": "C0001193",
    "id2": "MedGen UID:7858",
    "medgen_label": "Acrocephalosyndactyly type I",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7858",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007041",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007041",
    "nando_id": "NANDO:1200667"
  },
  {
    "id": "C0009207",
    "id2": "MedGen UID:40363",
    "medgen_label": "Cockayne syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/40363",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016006",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016006",
    "nando_id": "NANDO:1200677"
  },
  {
    "id": "C0010273",
    "id2": "MedGen UID:1162",
    "medgen_label": "Crouzon syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1162",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007405",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007405",
    "nando_id": "NANDO:1200666"
  },
  {
    "id": "C0010314",
    "id2": "MedGen UID:41345",
    "medgen_label": "5p partial monosomy syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/41345",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007404",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007404",
    "nando_id": "NANDO:1200684"
  },
  {
    "id": "C0162635",
    "id2": "MedGen UID:58144",
    "medgen_label": "Angelman syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/58144",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007113",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007113",
    "nando_id": "NANDO:1200686"
  },
  {
    "id": "C0175695",
    "id2": "MedGen UID:61232",
    "medgen_label": "Sotos syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/61232",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019349",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019349",
    "nando_id": "NANDO:1200679"
  },
  {
    "id": "C0175702",
    "id2": "MedGen UID:59799",
    "medgen_label": "Williams syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/59799",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008678",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008678",
    "nando_id": "NANDO:1200664"
  },
  {
    "id": "C0220658",
    "id2": "MedGen UID:67390",
    "medgen_label": "Pfeiffer syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/67390",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007043",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007043",
    "nando_id": "NANDO:1200668"
  },
  {
    "id": "C0221239",
    "id2": "MedGen UID:113155",
    "medgen_label": "Rapidly progressive glomerulonephritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/113155",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017236",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017236",
    "nando_id": "NANDO:1200714"
  },
  {
    "id": "C5234850",
    "id2": "MedGen UID:1714404",
    "medgen_label": "Antley-Bixler syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1714404",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008803",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008803",
    "nando_id": "NANDO:1200669"
  },
  {
    "id": "C0022716",
    "id2": "MedGen UID:44030",
    "medgen_label": "Menkes kinky-hair syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44030",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010651",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010651",
    "nando_id": "NANDO:1200653"
  },
  {
    "id": "C0024796",
    "id2": "MedGen UID:44287",
    "medgen_label": "Marfan syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44287",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007947",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007947",
    "nando_id": "NANDO:1200644"
  },
  {
    "id": "C0028326",
    "id2": "MedGen UID:18073",
    "medgen_label": "Noonan syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/18073",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018997",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018997",
    "nando_id": "NANDO:1200680"
  },
  {
    "id": "C0029411",
    "id2": "MedGen UID:18210",
    "medgen_label": "Pachydermoperiostosis syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/18210",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016620",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016620",
    "nando_id": "NANDO:1200642"
  },
  {
    "id": "C0268337",
    "id2": "MedGen UID:75670",
    "medgen_label": "Ehlers-Danlos syndrome, type 3",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75670",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007523",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007523",
    "nando_id": "NANDO:1200647"
  },
  {
    "id": "C0268338",
    "id2": "MedGen UID:82790",
    "medgen_label": "Ehlers-Danlos syndrome, type 4",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82790",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017314",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017314",
    "nando_id": "NANDO:1200648"
  },
  {
    "id": "C0268353",
    "id2": "MedGen UID:82793",
    "medgen_label": "Cutis laxa, X-linked",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82793",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010572",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010572",
    "nando_id": "NANDO:1200654"
  },
  {
    "id": "C1855675",
    "id2": "MedGen UID:340930",
    "medgen_label": "Joubert syndrome with oculorenal defect",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/340930",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009480",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009480",
    "nando_id": "NANDO:1200662"
  },
  {
    "id": "C1856113",
    "id2": "MedGen UID:341067",
    "medgen_label": "Mowat-Wilson syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/341067",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009341",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009341",
    "nando_id": "NANDO:1200663"
  },
  {
    "id": "C1857316",
    "id2": "MedGen UID:387795",
    "medgen_label": "Polycystic lipomembranous osteodysplasia with sclerosing leukoencephaly",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/387795",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009092",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009092",
    "nando_id": "NANDO:1200658"
  },
  {
    "id": "C1863557",
    "id2": "MedGen UID:350209",
    "medgen_label": "Blepharophimosis - intellectual disability syndrome, SBBYS type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/350209",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011365",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011365",
    "nando_id": "NANDO:1200681"
  },
  {
    "id": "C4225429",
    "id2": "MedGen UID:909864",
    "medgen_label": "Ehlers-Danlos syndrome, classic type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/909864",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007522",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007522",
    "nando_id": "NANDO:1200646"
  },
  {
    "id": "C4225671",
    "id2": "MedGen UID:902479",
    "medgen_label": "VATER association",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/902479",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008642",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008642",
    "nando_id": "NANDO:1200657"
  },
  {
    "id": "C0152101",
    "id2": "MedGen UID:57746",
    "medgen_label": "Hypoplastic left heart syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/57746",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0004933",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004933",
    "nando_id": "NANDO:1200705"
  },
  {
    "id": "C0344616",
    "id2": "MedGen UID:87489",
    "medgen_label": "Congenitally corrected transposition of the great arteries",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/87489",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016301",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016301",
    "nando_id": "NANDO:1200699"
  },
  {
    "id": "C0344622",
    "id2": "MedGen UID:488862",
    "medgen_label": "Double inlet left ventricle",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/488862",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015451",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015451",
    "nando_id": "NANDO:1200704"
  },
  {
    "id": "C0344975",
    "id2": "MedGen UID:87491",
    "medgen_label": "Pulmonary atresia with intact ventricular septum",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/87491",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009931",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009931",
    "nando_id": "NANDO:1200707"
  },
  {
    "id": "C0344976",
    "id2": "MedGen UID:87492",
    "medgen_label": "Pulmonary atresia with ventricular septal defect",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/87492",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008343",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008343",
    "nando_id": "NANDO:1200708"
  },
  {
    "id": "C1836929",
    "id2": "MedGen UID:323030",
    "medgen_label": "Emanuel syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/323030",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012176",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012176",
    "nando_id": "NANDO:1200689"
  },
  {
    "id": "C1839780",
    "id2": "MedGen UID:333403",
    "medgen_label": "Fragile X-associated tremor/ataxia syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/333403",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010382",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010382",
    "nando_id": "NANDO:1200691"
  },
  {
    "id": "C1842870",
    "id2": "MedGen UID:334629",
    "medgen_label": "Chromosome 1p36 deletion syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/334629",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011929",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011929",
    "nando_id": "NANDO:1200682"
  },
  {
    "id": "C1845055",
    "id2": "MedGen UID:337145",
    "medgen_label": "Alpha thalassemia-X-linked intellectual disability syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/337145",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010519",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010519",
    "nando_id": "NANDO:1200665"
  },
  {
    "id": "C4551623",
    "id2": "MedGen UID:1645042",
    "medgen_label": "Ehlers-Danlos syndrome, arthrochalasia type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1645042",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007525",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007525",
    "nando_id": "NANDO:1200650"
  },
  {
    "id": "C5671327",
    "id2": "MedGen UID:1812310",
    "medgen_label": "Dextro-looped transposition of the great arteries",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1812310",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019443",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019443",
    "nando_id": "NANDO:1200698"
  },
  {
    "id": "C0032339",
    "id2": "MedGen UID:10819",
    "medgen_label": "Rothmund-Thomson syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10819",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010002",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010002",
    "nando_id": "NANDO:1200671"
  },
  {
    "id": "C0032897",
    "id2": "MedGen UID:46057",
    "medgen_label": "Prader-Willi syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/46057",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008300",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008300",
    "nando_id": "NANDO:1200678"
  },
  {
    "id": "C0033847",
    "id2": "MedGen UID:18733",
    "medgen_label": "Pseudoxanthoma elasticum",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/18733",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0024308",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0024308",
    "nando_id": "NANDO:1200643"
  },
  {
    "id": "C0039685",
    "id2": "MedGen UID:21498",
    "medgen_label": "Tetralogy of Fallot",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21498",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008542",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008542",
    "nando_id": "NANDO:1200709"
  },
  {
    "id": "C0041207",
    "id2": "MedGen UID:52867",
    "medgen_label": "Persistent truncus arteriosus",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/52867",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018072",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018072",
    "nando_id": "NANDO:1200693"
  },
  {
    "id": "C0043119",
    "id2": "MedGen UID:12147",
    "medgen_label": "Werner syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/12147",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010196",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010196",
    "nando_id": "NANDO:1200676"
  },
  {
    "id": "C1956097",
    "id2": "MedGen UID:408255",
    "medgen_label": "4p partial monosomy syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/408255",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008684",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008684",
    "nando_id": "NANDO:1200683"
  },
  {
    "id": "C2700425",
    "id2": "MedGen UID:397792",
    "medgen_label": "Ehlers-Danlos syndrome, dermatosparaxis type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/397792",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009161",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009161",
    "nando_id": "NANDO:1200651"
  },
  {
    "id": "C0013069",
    "id2": "MedGen UID:41649",
    "medgen_label": "Double outlet right ventricle",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/41649",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018089",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018089",
    "nando_id": "NANDO:1200710"
  },
  {
    "id": "C0013481",
    "id2": "MedGen UID:4435",
    "medgen_label": "Ebstein anomaly",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/4435",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009144",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009144",
    "nando_id": "NANDO:1200711"
  },
  {
    "id": "C0013720",
    "id2": "MedGen UID:41720",
    "medgen_label": "Ehlers-Danlos syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/41720",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020066",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020066",
    "nando_id": "NANDO:1200645"
  },
  {
    "id": "C0016667",
    "id2": "MedGen UID:8912",
    "medgen_label": "Fragile X syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/8912",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010383",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010383",
    "nando_id": "NANDO:1200692"
  },
  {
    "id": "C0019202",
    "id2": "MedGen UID:42426",
    "medgen_label": "Wilson disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/42426",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010200",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010200",
    "nando_id": "NANDO:1200655"
  },
  {
    "id": "C0020630",
    "id2": "MedGen UID:43799",
    "medgen_label": "Hypophosphatasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/43799",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018570",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018570",
    "nando_id": "NANDO:1200656"
  },
  {
    "id": "C0243002",
    "id2": "MedGen UID:67034",
    "medgen_label": "Tricuspid atresia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/67034",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011514",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011514",
    "nando_id": "NANDO:1200706"
  },
  {
    "id": "C0265210",
    "id2": "MedGen UID:120511",
    "medgen_label": "Weaver syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120511",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010193",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010193",
    "nando_id": "NANDO:1200659"
  },
  {
    "id": "C0265234",
    "id2": "MedGen UID:82693",
    "medgen_label": "Melnick-Fraser syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82693",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007029",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007029",
    "nando_id": "NANDO:1200675"
  },
  {
    "id": "C0265252",
    "id2": "MedGen UID:75556",
    "medgen_label": "Coffin-Lowry syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75556",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010561",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010561",
    "nando_id": "NANDO:1200660"
  },
  {
    "id": "C0265338",
    "id2": "MedGen UID:75565",
    "medgen_label": "Coffin-Siris syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75565",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015452",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015452",
    "nando_id": "NANDO:1200670"
  },
  {
    "id": "C0795864",
    "id2": "MedGen UID:162881",
    "medgen_label": "Smith-Magenis syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/162881",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008434",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008434",
    "nando_id": "NANDO:1200687"
  },
  {
    "id": "C0795949",
    "id2": "MedGen UID:167086",
    "medgen_label": "Galloway-Mowat syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/167086",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009627",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009627",
    "nando_id": "NANDO:1200713"
  },
  {
    "id": "C0796004",
    "id2": "MedGen UID:162897",
    "medgen_label": "Kabuki syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/162897",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016512",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016512",
    "nando_id": "NANDO:1200672"
  },
  {
    "id": "C5679612",
    "id2": "MedGen UID:1826007",
    "medgen_label": "Joubert syndrome and related disorders",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1826007",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015369",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015369",
    "nando_id": "NANDO:1200661"
  },
  {
    "id": "C5680251",
    "id2": "MedGen UID:1843450",
    "medgen_label": "Paternal uniparental disomy of chromosome 14",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1843450",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011975",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011975",
    "nando_id": "NANDO:1200685"
  },
  {
    "id": "CN294181",
    "id2": "MedGen UID:977689",
    "medgen_label": "22q11.2 deletion syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/977689",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018923",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018923",
    "nando_id": "NANDO:1200688"
  },
  {
    "id": "C1847501",
    "id2": "MedGen UID:337833",
    "medgen_label": "GLUT1 deficiency syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/337833",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000188",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000188",
    "nando_id": "NANDO:1200799"
  },
  {
    "id": "C1848552",
    "id2": "MedGen UID:341253",
    "medgen_label": "Methylmalonic aciduria and homocystinuria type cblD",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/341253",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010185",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010185",
    "nando_id": "NANDO:1200797"
  },
  {
    "id": "C1849678",
    "id2": "MedGen UID:376636",
    "medgen_label": "Acyl-CoA oxidase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/376636",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009919",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009919",
    "nando_id": "NANDO:1200765"
  },
  {
    "id": "C1855102",
    "id2": "MedGen UID:344420",
    "medgen_label": "Methylmalonic aciduria, cblB type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/344420",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009614",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009614",
    "nando_id": "NANDO:1200796"
  },
  {
    "id": "C1855109",
    "id2": "MedGen UID:344422",
    "medgen_label": "Methylmalonic aciduria, cblA type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/344422",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009613",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009613",
    "nando_id": "NANDO:1200795"
  },
  {
    "id": "C1855114",
    "id2": "MedGen UID:344424",
    "medgen_label": "Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/344424",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009612",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009612",
    "nando_id": "NANDO:1200794"
  },
  {
    "id": "C0221757",
    "id2": "MedGen UID:67461",
    "medgen_label": "Alpha-1-antitrypsin deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/67461",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013282",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013282",
    "nando_id": "NANDO:1200755"
  },
  {
    "id": "C1970472",
    "id2": "MedGen UID:410079",
    "medgen_label": "Autoimmune pulmonary alveolar proteinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/410079",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012579",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012579",
    "nando_id": "NANDO:1200747"
  },
  {
    "id": "C1970472",
    "id2": "MedGen UID:410079",
    "medgen_label": "Autoimmune pulmonary alveolar proteinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/410079",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0012579",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012579",
    "nando_id": "NANDO:1200748"
  },
  {
    "id": "C3150990",
    "id2": "MedGen UID:462340",
    "medgen_label": "Sterol carrier protein 2 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/462340",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013391",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013391",
    "nando_id": "NANDO:1200767"
  },
  {
    "id": "C0024776",
    "id2": "MedGen UID:6217",
    "medgen_label": "Maple syrup urine disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6217",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009563",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009563",
    "nando_id": "NANDO:1200791"
  },
  {
    "id": "C0027721",
    "id2": "MedGen UID:10307",
    "medgen_label": "Lipoid nephrosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10307",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006835",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006835",
    "nando_id": "NANDO:1200720"
  },
  {
    "id": "C0031485",
    "id2": "MedGen UID:19244",
    "medgen_label": "Phenylketonuria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/19244",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009861",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009861",
    "nando_id": "NANDO:1200785"
  },
  {
    "id": "C0031485",
    "id2": "MedGen UID:19244",
    "medgen_label": "Phenylketonuria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/19244",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009861",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009861",
    "nando_id": "NANDO:1200784"
  },
  {
    "id": "C0031880",
    "id2": "MedGen UID:18472",
    "medgen_label": "Extreme obesity with alveolar hypoventilation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/18472",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009763",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009763",
    "nando_id": "NANDO:1200752"
  },
  {
    "id": "C0268164",
    "id2": "MedGen UID:75658",
    "medgen_label": "Primary hyperoxaluria, type I",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75658",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009823",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009823",
    "nando_id": "NANDO:1200773"
  },
  {
    "id": "C0268419",
    "id2": "MedGen UID:75679",
    "medgen_label": "Acatalasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75679",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013571",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013571",
    "nando_id": "NANDO:1200774"
  },
  {
    "id": "C0268487",
    "id2": "MedGen UID:75687",
    "medgen_label": "Tyrosinemia type II",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75687",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010160",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010160",
    "nando_id": "NANDO:1200789"
  },
  {
    "id": "C0268490",
    "id2": "MedGen UID:75688",
    "medgen_label": "Tyrosinemia type I",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75688",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010161",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010161",
    "nando_id": "NANDO:1200788"
  },
  {
    "id": "C0268575",
    "id2": "MedGen UID:82822",
    "medgen_label": "Isovaleryl-CoA dehydrogenase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82822",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009475",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009475",
    "nando_id": "NANDO:1200798"
  },
  {
    "id": "C0268579",
    "id2": "MedGen UID:75694",
    "medgen_label": "Propionic acidemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75694",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011628",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011628",
    "nando_id": "NANDO:1200792"
  },
  {
    "id": "C0268583",
    "id2": "MedGen UID:120654",
    "medgen_label": "Methylmalonic acidemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120654",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002012",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002012",
    "nando_id": "NANDO:1200793"
  },
  {
    "id": "C0268595",
    "id2": "MedGen UID:124337",
    "medgen_label": "Glutaric aciduria, type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/124337",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009281",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009281",
    "nando_id": "NANDO:1200800"
  },
  {
    "id": "C0268596",
    "id2": "MedGen UID:75696",
    "medgen_label": "Multiple acyl-CoA dehydrogenase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75696",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009282",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009282",
    "nando_id": "NANDO:1200801"
  },
  {
    "id": "C0268623",
    "id2": "MedGen UID:78694",
    "medgen_label": "Tyrosinemia type III",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78694",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010162",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010162",
    "nando_id": "NANDO:1200790"
  },
  {
    "id": "C0268689",
    "id2": "MedGen UID:124344",
    "medgen_label": "Vitamin D-dependent rickets, type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/124344",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009924",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009924",
    "nando_id": "NANDO:1200782"
  },
  {
    "id": "C0403416",
    "id2": "MedGen UID:96040",
    "medgen_label": "Crescentic glomerulonephritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/96040",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001645",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001645",
    "nando_id": "NANDO:1200723"
  },
  {
    "id": "C0403529",
    "id2": "MedGen UID:140788",
    "medgen_label": "Anti-glomerular basement membrane disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/140788",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009303",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009303",
    "nando_id": "NANDO:1200717"
  },
  {
    "id": "C0403529",
    "id2": "MedGen UID:140788",
    "medgen_label": "Anti-glomerular basement membrane disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/140788",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009303",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009303",
    "nando_id": "NANDO:1200718"
  },
  {
    "id": "C1857242",
    "id2": "MedGen UID:341734",
    "medgen_label": "Rhizomelic chondrodysplasia punctata type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/341734",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009112",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009112",
    "nando_id": "NANDO:1200771"
  },
  {
    "id": "C1859133",
    "id2": "MedGen UID:347072",
    "medgen_label": "Rhizomelic chondrodysplasia punctata type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/347072",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008972",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008972",
    "nando_id": "NANDO:1200763"
  },
  {
    "id": "C3280428",
    "id2": "MedGen UID:482058",
    "medgen_label": "Alpha-methylacyl-CoA racemase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/482058",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013681",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013681",
    "nando_id": "NANDO:1200768"
  },
  {
    "id": "C3554330",
    "id2": "MedGen UID:767244",
    "medgen_label": "Immunoglobulin-mediated membranoproliferative glomerulonephritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/767244",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014005",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014005",
    "nando_id": "NANDO:1200726"
  },
  {
    "id": "C3711368",
    "id2": "MedGen UID:777976",
    "medgen_label": "Hereditary pulmonary alveolar proteinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/777976",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0012580",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012580",
    "nando_id": "NANDO:1200746"
  },
  {
    "id": "C3711368",
    "id2": "MedGen UID:777976",
    "medgen_label": "Hereditary pulmonary alveolar proteinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/777976",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012580",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012580",
    "nando_id": "NANDO:1200750"
  },
  {
    "id": "C4082171",
    "id2": "MedGen UID:907954",
    "medgen_label": "Congenital hyperammonemia, type I",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/907954",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009376",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009376",
    "nando_id": "NANDO:1200803"
  },
  {
    "id": "C0154246",
    "id2": "MedGen UID:57586",
    "medgen_label": "Disorder of the urea cycle metabolism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/57586",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0004739",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004739",
    "nando_id": "NANDO:1200802"
  },
  {
    "id": "C0342870",
    "id2": "MedGen UID:137982",
    "medgen_label": "Bifunctional peroxisomal enzyme deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/137982",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009855",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009855",
    "nando_id": "NANDO:1200766"
  },
  {
    "id": "C0733682",
    "id2": "MedGen UID:196551",
    "medgen_label": "Familial X-linked hypophosphatemic vitamin D refractory rickets",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/196551",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0010619",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010619",
    "nando_id": "NANDO:1200779"
  },
  {
    "id": "C1838612",
    "id2": "MedGen UID:374012",
    "medgen_label": "Rhizomelic chondrodysplasia punctata type 3",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/374012",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010823",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010823",
    "nando_id": "NANDO:1200772"
  },
  {
    "id": "C4551966",
    "id2": "MedGen UID:1645412",
    "medgen_label": "Encephalopathy due to GLUT1 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1645412",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0011724",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011724",
    "nando_id": "NANDO:1200799"
  },
  {
    "id": "C0034960",
    "id2": "MedGen UID:11161",
    "medgen_label": "Phytanic acid storage disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/11161",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009958",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009958",
    "nando_id": "NANDO:1200769"
  },
  {
    "id": "C2748783",
    "id2": "MedGen UID:411667",
    "medgen_label": "Vitamin D-dependent rickets, type 2B",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/411667",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0010931",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010931",
    "nando_id": "NANDO:1200779"
  },
  {
    "id": "C5400698",
    "id2": "MedGen UID:1763046",
    "medgen_label": "Pulmonary alveolar proteinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1763046",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001437",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001437",
    "nando_id": "NANDO:1200746"
  },
  {
    "id": "C0017665",
    "id2": "MedGen UID:42231",
    "medgen_label": "Membranous nephropathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/42231",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005376",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005376",
    "nando_id": "NANDO:1200721"
  },
  {
    "id": "C0020626",
    "id2": "MedGen UID:6985",
    "medgen_label": "Hypoparathyroidism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6985",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001220",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001220",
    "nando_id": "NANDO:1200775"
  },
  {
    "id": "C0020807",
    "id2": "MedGen UID:9403",
    "medgen_label": "Idiopathic pulmonary hemosiderosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9403",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008346",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008346",
    "nando_id": "NANDO:1200751"
  },
  {
    "id": "C1332309",
    "id2": "MedGen UID:231383",
    "medgen_label": "Anti-basement membrane glomerulonephritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/231383",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0003136",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003136",
    "nando_id": "NANDO:1200717"
  },
  {
    "id": "CN327126",
    "id2": "MedGen UID:1008296",
    "medgen_label": "Inherited focal segmental glomerulosclerosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1008296",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005363",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005363",
    "nando_id": "NANDO:1200722"
  },
  {
    "id": "C1704375",
    "id2": "MedGen UID:309957",
    "medgen_label": "Hypophosphatemic rickets",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/309957",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0024300",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0024300",
    "nando_id": "NANDO:1200780"
  },
  {
    "id": "C1704375",
    "id2": "MedGen UID:309957",
    "medgen_label": "Hypophosphatemic rickets",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/309957",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0024300",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0024300",
    "nando_id": "NANDO:1200778"
  },
  {
    "id": "C1832200",
    "id2": "MedGen UID:330407",
    "medgen_label": "Peroxisome biogenesis disorder",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/330407",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019234",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019234",
    "nando_id": "NANDO:1200759"
  },
  {
    "id": "C0006272",
    "id2": "MedGen UID:665",
    "medgen_label": "Bronchiolitis obliterans with obstructive pulmonary disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/665",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015265",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015265",
    "nando_id": "NANDO:1200745"
  },
  {
    "id": "C0162283",
    "id2": "MedGen UID:57876",
    "medgen_label": "Nephrogenic diabetes insipidus",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/57876",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016383",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016383",
    "nando_id": "NANDO:1200742"
  },
  {
    "id": "C0221239",
    "id2": "MedGen UID:113155",
    "medgen_label": "Rapidly progressive glomerulonephritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/113155",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0017236",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017236",
    "nando_id": "NANDO:1200723"
  },
  {
    "id": "C0221468",
    "id2": "MedGen UID:526251",
    "medgen_label": "Vitamin D-dependent rickets",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/526251",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0024299",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0024299",
    "nando_id": "NANDO:1200781"
  },
  {
    "id": "C0406810",
    "id2": "MedGen UID:140810",
    "medgen_label": "Carney complex",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/140810",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015285",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015285",
    "nando_id": "NANDO:1200756"
  },
  {
    "id": "C0268743",
    "id2": "MedGen UID:124345",
    "medgen_label": "Mesangiocapillary glomerulonephritis, type II",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/124345",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019736",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019736",
    "nando_id": "NANDO:1200739"
  },
  {
    "id": "C3496337",
    "id2": "MedGen UID:501252",
    "medgen_label": "Idiopathic nephrotic syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/501252",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018170",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018170",
    "nando_id": "NANDO:1200719"
  },
  {
    "id": "C3536983",
    "id2": "MedGen UID:760752",
    "medgen_label": "Vitamin D-dependent rickets, type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/760752",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019642",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019642",
    "nando_id": "NANDO:1200783"
  },
  {
    "id": "C3873302",
    "id2": "MedGen UID:845105",
    "medgen_label": "Secondary pulmonary alveolar proteinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/845105",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018483",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018483",
    "nando_id": "NANDO:1200749"
  },
  {
    "id": "C0033806",
    "id2": "MedGen UID:46178",
    "medgen_label": "Pseudohypoparathyroidism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/46178",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019992",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019992",
    "nando_id": "NANDO:1200776"
  },
  {
    "id": "C0039445",
    "id2": "MedGen UID:52657",
    "medgen_label": "Hereditary hemorrhagic telangiectasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/52657",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019180",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019180",
    "nando_id": "NANDO:1200744"
  },
  {
    "id": "C0043207",
    "id2": "MedGen UID:21923",
    "medgen_label": "Wolfram syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21923",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018105",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018105",
    "nando_id": "NANDO:1200757"
  },
  {
    "id": "C0043459",
    "id2": "MedGen UID:21958",
    "medgen_label": "Zellweger spectrum disorders",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21958",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019609",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019609",
    "nando_id": "NANDO:1200760"
  },
  {
    "id": "C0282488",
    "id2": "MedGen UID:129176",
    "medgen_label": "Interstitial cystitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/129176",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018301",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018301",
    "nando_id": "NANDO:1200743"
  },
  {
    "id": "C0282528",
    "id2": "MedGen UID:129185",
    "medgen_label": "Peroxisomal disorder",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/129185",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019053",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019053",
    "nando_id": "NANDO:1200758"
  },
  {
    "id": "C0751436",
    "id2": "MedGen UID:199656",
    "medgen_label": "Hyperphenylalaninemia due to tetrahydrobiopterin deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/199656",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016543",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016543",
    "nando_id": "NANDO:1200786"
  },
  {
    "id": "C5681192",
    "id2": "MedGen UID:1842510",
    "medgen_label": "Disorder of plasmalogens biosynthesis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1842510",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017986",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017986",
    "nando_id": "NANDO:1200770"
  },
  {
    "id": "C5681280",
    "id2": "MedGen UID:1843097",
    "medgen_label": "Disorder of peroxisomal beta oxidation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1843097",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019233",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019233",
    "nando_id": "NANDO:1200764"
  },
  {
    "id": "CN304703",
    "id2": "MedGen UID:988496",
    "medgen_label": "Primary membranoproliferative glomerulonephritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/988496",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018904",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018904",
    "nando_id": "NANDO:1200725"
  },
  {
    "id": "C0000744",
    "id2": "MedGen UID:1253",
    "medgen_label": "Abetalipoproteinaemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1253",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008692",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008692",
    "nando_id": "NANDO:1200857"
  },
  {
    "id": "C0001080",
    "id2": "MedGen UID:1289",
    "medgen_label": "Achondroplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1289",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007037",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007037",
    "nando_id": "NANDO:1200877"
  },
  {
    "id": "C0162531",
    "id2": "MedGen UID:57931",
    "medgen_label": "Hereditary coproporphyria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/57931",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007369",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007369",
    "nando_id": "NANDO:1200813"
  },
  {
    "id": "C0162532",
    "id2": "MedGen UID:58118",
    "medgen_label": "Variegate porphyria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/58118",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008297",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008297",
    "nando_id": "NANDO:1200814"
  },
  {
    "id": "C0162565",
    "id2": "MedGen UID:56452",
    "medgen_label": "Acute intermittent porphyria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/56452",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008294",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008294",
    "nando_id": "NANDO:1200812"
  },
  {
    "id": "C0162568",
    "id2": "MedGen UID:56455",
    "medgen_label": "Erythropoietic protoporphyria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/56455",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001676",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001676",
    "nando_id": "NANDO:1200815"
  },
  {
    "id": "C0221032",
    "id2": "MedGen UID:67438",
    "medgen_label": "Congenital generalized lipodystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/67438",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006536",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006536",
    "nando_id": "NANDO:1200859"
  },
  {
    "id": "C0022739",
    "id2": "MedGen UID:9646",
    "medgen_label": "Angioosteohypertrophic syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9646",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007864",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007864",
    "nando_id": "NANDO:1200884"
  },
  {
    "id": "C0023787",
    "id2": "MedGen UID:6111",
    "medgen_label": "Lipodystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6111",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006573",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006573",
    "nando_id": "NANDO:1200858"
  },
  {
    "id": "C0027122",
    "id2": "MedGen UID:6503",
    "medgen_label": "Myositis ossificans",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6503",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0003964",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003964",
    "nando_id": "NANDO:1200871"
  },
  {
    "id": "C0029436",
    "id2": "MedGen UID:45247",
    "medgen_label": "Disappearing bone disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/45247",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0003157",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003157",
    "nando_id": "NANDO:1200878"
  },
  {
    "id": "C0029438",
    "id2": "MedGen UID:45248",
    "medgen_label": "Gorham-Stout disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/45248",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007414",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007414",
    "nando_id": "NANDO:1200878"
  },
  {
    "id": "C4692546",
    "id2": "MedGen UID:1643471",
    "medgen_label": "Protoporphyria, erythropoietic, 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1643471",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0008319",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008319",
    "nando_id": "NANDO:1200815"
  },
  {
    "id": "C5676874",
    "id2": "MedGen UID:1801596",
    "medgen_label": "Congenital dyserythropoietic anemia, type III",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1801596",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007109",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007109",
    "nando_id": "NANDO:1200888"
  },
  {
    "id": "C0038013",
    "id2": "MedGen UID:11561",
    "medgen_label": "Ankylosing spondylitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/11561",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005306",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005306",
    "nando_id": "NANDO:1200870"
  },
  {
    "id": "C1868678",
    "id2": "MedGen UID:358383",
    "medgen_label": "Thanatophoric dysplasia type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/358383",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008546",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008546",
    "nando_id": "NANDO:1200875"
  },
  {
    "id": "C0016037",
    "id2": "MedGen UID:4698",
    "medgen_label": "Progressive myositis ossificans",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/4698",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007606",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007606",
    "nando_id": "NANDO:1200871"
  },
  {
    "id": "C0017919",
    "id2": "MedGen UID:6639",
    "medgen_label": "Glycogen storage disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6639",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0002412",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002412",
    "nando_id": "NANDO:1200838"
  },
  {
    "id": "C0017920",
    "id2": "MedGen UID:6640",
    "medgen_label": "Glycogen storage disease, type I",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6640",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0002413",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002413",
    "nando_id": "NANDO:1200840"
  },
  {
    "id": "C1300257",
    "id2": "MedGen UID:226975",
    "medgen_label": "Thanatophoric dysplasia, type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/226975",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008547",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008547",
    "nando_id": "NANDO:1200876"
  },
  {
    "id": "C1850568",
    "id2": "MedGen UID:376827",
    "medgen_label": "Proteosome-associated autoinflammatory syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/376827",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009726",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009726",
    "nando_id": "NANDO:1200867"
  },
  {
    "id": "C0162530",
    "id2": "MedGen UID:102408",
    "medgen_label": "Cutaneous porphyria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/102408",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009902",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009902",
    "nando_id": "NANDO:1200817"
  },
  {
    "id": "C0220754",
    "id2": "MedGen UID:66323",
    "medgen_label": "Biotinidase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/66323",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009665",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009665",
    "nando_id": "NANDO:1200822"
  },
  {
    "id": "C0410422",
    "id2": "MedGen UID:140822",
    "medgen_label": "Chronic multifocal osteomyelitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/140822",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009813",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009813",
    "nando_id": "NANDO:1200869"
  },
  {
    "id": "C1970848",
    "id2": "MedGen UID:410166",
    "medgen_label": "Glycogen storage disease due to phosphoglycerate kinase 1 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/410166",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010392",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010392",
    "nando_id": "NANDO:1200831"
  },
  {
    "id": "C2677889",
    "id2": "MedGen UID:394385",
    "medgen_label": "X-linked erythropoietic protoporphyria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/394385",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010420",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010420",
    "nando_id": "NANDO:1200818"
  },
  {
    "id": "C0023195",
    "id2": "MedGen UID:9698",
    "medgen_label": "Norum disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9698",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009515",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009515",
    "nando_id": "NANDO:1200852"
  },
  {
    "id": "C0268146",
    "id2": "MedGen UID:78644",
    "medgen_label": "Glucose-6-phosphate transport defect",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78644",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009288",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009288",
    "nando_id": "NANDO:1200841"
  },
  {
    "id": "C0268149",
    "id2": "MedGen UID:120613",
    "medgen_label": "Glycogen storage disease type X",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120613",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009865",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009865",
    "nando_id": "NANDO:1200832"
  },
  {
    "id": "C0268151",
    "id2": "MedGen UID:82777",
    "medgen_label": "Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82777",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009258",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009258",
    "nando_id": "NANDO:1200851"
  },
  {
    "id": "C0268542",
    "id2": "MedGen UID:75692",
    "medgen_label": "Ornithine carbamoyltransferase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75692",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010703",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010703",
    "nando_id": "NANDO:1200804"
  },
  {
    "id": "C0268543",
    "id2": "MedGen UID:120649",
    "medgen_label": "Hyperammonemia, type III",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120649",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009377",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009377",
    "nando_id": "NANDO:1200808"
  },
  {
    "id": "C0268547",
    "id2": "MedGen UID:78687",
    "medgen_label": "Argininosuccinate lyase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78687",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008815",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008815",
    "nando_id": "NANDO:1200806"
  },
  {
    "id": "C0268548",
    "id2": "MedGen UID:78688",
    "medgen_label": "Arginase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78688",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008814",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008814",
    "nando_id": "NANDO:1200807"
  },
  {
    "id": "C0268581",
    "id2": "MedGen UID:120653",
    "medgen_label": "Holocarboxylase synthetase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120653",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009666",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009666",
    "nando_id": "NANDO:1200821"
  },
  {
    "id": "C0268647",
    "id2": "MedGen UID:75704",
    "medgen_label": "Lysinuric protein intolerance",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75704",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009109",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009109",
    "nando_id": "NANDO:1200809"
  },
  {
    "id": "C0398691",
    "id2": "MedGen UID:140768",
    "medgen_label": "Hyperimmunoglobulin D with periodic fever",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/140768",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009849",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009849",
    "nando_id": "NANDO:1200866"
  },
  {
    "id": "C0543514",
    "id2": "MedGen UID:107772",
    "medgen_label": "Glycogen storage disease IXb",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/107772",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009868",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009868",
    "nando_id": "NANDO:1200848"
  },
  {
    "id": "C1855861",
    "id2": "MedGen UID:343430",
    "medgen_label": "Glycogen storage disorder due to hepatic glycogen synthase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/343430",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009414",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009414",
    "nando_id": "NANDO:1200838"
  },
  {
    "id": "C1855861",
    "id2": "MedGen UID:343430",
    "medgen_label": "Glycogen storage disorder due to hepatic glycogen synthase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/343430",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009414",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009414",
    "nando_id": "NANDO:1200824"
  },
  {
    "id": "C1858361",
    "id2": "MedGen UID:346801",
    "medgen_label": "Pyogenic arthritis-pyoderma gangrenosum-acne syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/346801",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011462",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011462",
    "nando_id": "NANDO:1200868"
  },
  {
    "id": "C3694531",
    "id2": "MedGen UID:854172",
    "medgen_label": "Glycogen storage disease IXa1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/854172",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010598",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010598",
    "nando_id": "NANDO:1200847"
  },
  {
    "id": "C4721769",
    "id2": "MedGen UID:1648491",
    "medgen_label": "Citrullinemia type I",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1648491",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008988",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008988",
    "nando_id": "NANDO:1200805"
  },
  {
    "id": "C0342705",
    "id2": "MedGen UID:83348",
    "medgen_label": "Congenital defect of folate absorption",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/83348",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009238",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009238",
    "nando_id": "NANDO:1200810"
  },
  {
    "id": "C0342907",
    "id2": "MedGen UID:87466",
    "medgen_label": "Sitosterolemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/87466",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008863",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008863",
    "nando_id": "NANDO:1200853"
  },
  {
    "id": "C1845151",
    "id2": "MedGen UID:335112",
    "medgen_label": "Glycogen storage disease IXd",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/335112",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010362",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010362",
    "nando_id": "NANDO:1200830"
  },
  {
    "id": "C0039292",
    "id2": "MedGen UID:52644",
    "medgen_label": "Tangier disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/52644",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008783",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008783",
    "nando_id": "NANDO:1200854"
  },
  {
    "id": "C0017921",
    "id2": "MedGen UID:5340",
    "medgen_label": "Glycogen storage disease, type II",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5340",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009290",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009290",
    "nando_id": "NANDO:1200825"
  },
  {
    "id": "C0017922",
    "id2": "MedGen UID:6641",
    "medgen_label": "Glycogen storage disease type III",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6641",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009291",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009291",
    "nando_id": "NANDO:1200844"
  },
  {
    "id": "C0017922",
    "id2": "MedGen UID:6641",
    "medgen_label": "Glycogen storage disease type III",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6641",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009291",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009291",
    "nando_id": "NANDO:1200826"
  },
  {
    "id": "C0017923",
    "id2": "MedGen UID:6642",
    "medgen_label": "Glycogen storage disease, type IV",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6642",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009292",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009292",
    "nando_id": "NANDO:1200850"
  },
  {
    "id": "C0017923",
    "id2": "MedGen UID:6642",
    "medgen_label": "Glycogen storage disease, type IV",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6642",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009292",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009292",
    "nando_id": "NANDO:1200827"
  },
  {
    "id": "C0017924",
    "id2": "MedGen UID:5341",
    "medgen_label": "Glycogen storage disease, type V",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5341",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009293",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009293",
    "nando_id": "NANDO:1200828"
  },
  {
    "id": "C0017925",
    "id2": "MedGen UID:6643",
    "medgen_label": "Glycogen storage disease, type VI",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6643",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009294",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009294",
    "nando_id": "NANDO:1200846"
  },
  {
    "id": "C0017926",
    "id2": "MedGen UID:5342",
    "medgen_label": "Glycogen storage disease, type VII",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5342",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009295",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009295",
    "nando_id": "NANDO:1200829"
  },
  {
    "id": "C0017926",
    "id2": "MedGen UID:5342",
    "medgen_label": "Glycogen storage disease, type VII",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5342",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009295",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009295",
    "nando_id": "NANDO:1200823"
  },
  {
    "id": "C0238052",
    "id2": "MedGen UID:116041",
    "medgen_label": "Cholestanol storage disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/116041",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008948",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008948",
    "nando_id": "NANDO:1200856"
  },
  {
    "id": "C1306589",
    "id2": "MedGen UID:266296",
    "medgen_label": "Congenital dyserythropoietic anemia, type II",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/266296",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009134",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009134",
    "nando_id": "NANDO:1200887"
  },
  {
    "id": "CN293506",
    "id2": "MedGen UID:976601",
    "medgen_label": "Autosomal recessive familial Mediterranean fever",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/976601",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009572",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009572",
    "nando_id": "NANDO:1200864"
  },
  {
    "id": "C0002876",
    "id2": "MedGen UID:8064",
    "medgen_label": "Congenital dyserythropoietic anemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/8064",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019403",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019403",
    "nando_id": "NANDO:1200885"
  },
  {
    "id": "C0162566",
    "id2": "MedGen UID:56453",
    "medgen_label": "Porphyria cutanea tarda",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/56453",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015104",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015104",
    "nando_id": "NANDO:1200816"
  },
  {
    "id": "C0162569",
    "id2": "MedGen UID:57940",
    "medgen_label": "Hepatoerythropoietic porphyria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/57940",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019799",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019799",
    "nando_id": "NANDO:1200819"
  },
  {
    "id": "C0205828",
    "id2": "MedGen UID:104729",
    "medgen_label": "Cavernous lymphangioma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/104729",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0019328",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019328",
    "nando_id": "NANDO:1200881"
  },
  {
    "id": "C0220989",
    "id2": "MedGen UID:66352",
    "medgen_label": "Acquired partial lipodystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/66352",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012104",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012104",
    "nando_id": "NANDO:1200862"
  },
  {
    "id": "C2931345",
    "id2": "MedGen UID:419390",
    "medgen_label": "Glycogen storage disease type 1 due to SLC37A4 mutation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/419390",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0023258",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0023258",
    "nando_id": "NANDO:1200841"
  },
  {
    "id": "C2931743",
    "id2": "MedGen UID:419152",
    "medgen_label": "Glycogen storage disease due to lactate dehydrogenase M-subunit deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/419152",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013047",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013047",
    "nando_id": "NANDO:1200833"
  },
  {
    "id": "C3150754",
    "id2": "MedGen UID:462104",
    "medgen_label": "Glycogen storage disease XV",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/462104",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013291",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013291",
    "nando_id": "NANDO:1200837"
  },
  {
    "id": "C5779633",
    "id2": "MedGen UID:1830326",
    "medgen_label": "LCAT deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1830326",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018999",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018999",
    "nando_id": "NANDO:1200852"
  },
  {
    "id": "C5848305",
    "id2": "MedGen UID:1844832",
    "medgen_label": "Porphyria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1844832",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0037939",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0037939",
    "nando_id": "NANDO:1200811"
  },
  {
    "id": "C0026755",
    "id2": "MedGen UID:10119",
    "medgen_label": "Multiple carboxylase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10119",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015454",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015454",
    "nando_id": "NANDO:1200820"
  },
  {
    "id": "C0029434",
    "id2": "MedGen UID:45246",
    "medgen_label": "Osteogenesis imperfecta",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/45246",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019019",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019019",
    "nando_id": "NANDO:1200873"
  },
  {
    "id": "C0031069",
    "id2": "MedGen UID:45811",
    "medgen_label": "Familial Mediterranean fever",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/45811",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018088",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018088",
    "nando_id": "NANDO:1200863"
  },
  {
    "id": "C0039743",
    "id2": "MedGen UID:21124",
    "medgen_label": "Thanatophoric dysplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21124",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017042",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017042",
    "nando_id": "NANDO:1200874"
  },
  {
    "id": "C0271693",
    "id2": "MedGen UID:543499",
    "medgen_label": "Acquired generalized lipodystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/543499",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019193",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019193",
    "nando_id": "NANDO:1200860"
  },
  {
    "id": "C0271694",
    "id2": "MedGen UID:124408",
    "medgen_label": "Familial partial lipodystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/124408",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020088",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020088",
    "nando_id": "NANDO:1200861"
  },
  {
    "id": "C0271933",
    "id2": "MedGen UID:82891",
    "medgen_label": "Congenital dyserythropoietic anemia, type I",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82891",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020337",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020337",
    "nando_id": "NANDO:1200886"
  },
  {
    "id": "C0272066",
    "id2": "MedGen UID:82895",
    "medgen_label": "HNSHA due to aldolase A deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82895",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012747",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012747",
    "nando_id": "NANDO:1200834"
  },
  {
    "id": "C1959626",
    "id2": "MedGen UID:368373",
    "medgen_label": "Mevalonic aciduria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/368373",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0012481",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012481",
    "nando_id": "NANDO:1200866"
  },
  {
    "id": "C2751643",
    "id2": "MedGen UID:442778",
    "medgen_label": "Glycogen storage disease IXc",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/442778",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013091",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013091",
    "nando_id": "NANDO:1200849"
  },
  {
    "id": "C2752015",
    "id2": "MedGen UID:414536",
    "medgen_label": "PGM1-congenital disorder of glycosylation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/414536",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013968",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013968",
    "nando_id": "NANDO:1200836"
  },
  {
    "id": "C2752027",
    "id2": "MedGen UID:442873",
    "medgen_label": "Glycogen storage disease due to muscle beta-enolase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/442873",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013046",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013046",
    "nando_id": "NANDO:1200835"
  },
  {
    "id": "CN262437",
    "id2": "MedGen UID:945467",
    "medgen_label": "Berardinelli-Seip congenital lipodystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/945467",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018883",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018883",
    "nando_id": "NANDO:1200859"
  },
  {
    "id": "CN283243",
    "id2": "MedGen UID:966646",
    "medgen_label": "Autosomal erythropoietic protoporphyria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/966646",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0019263",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019263",
    "nando_id": "NANDO:1200815"
  },
  {
    "id": "C0001169",
    "id2": "MedGen UID:98",
    "medgen_label": "Acquired coagulation factor deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/98",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020599",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020599",
    "nando_id": "NANDO:1200896"
  },
  {
    "id": "C0005411",
    "id2": "MedGen UID:14117",
    "medgen_label": "Biliary atresia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/14117",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008867",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008867",
    "nando_id": "NANDO:1200913"
  },
  {
    "id": "C0010674",
    "id2": "MedGen UID:41393",
    "medgen_label": "Cystic fibrosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/41393",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009061",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009061",
    "nando_id": "NANDO:1200922"
  },
  {
    "id": "C0221018",
    "id2": "MedGen UID:65119",
    "medgen_label": "Hereditary sideroblastic anemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/65119",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020099",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020099",
    "nando_id": "NANDO:1200892"
  },
  {
    "id": "C2609129",
    "id2": "MedGen UID:750633",
    "medgen_label": "Autoimmune pancreatitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/750633",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015175",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015175",
    "nando_id": "NANDO:1200925"
  },
  {
    "id": "C5392056",
    "id2": "MedGen UID:1708840",
    "medgen_label": "IgG4-related kidney disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1708840",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018671",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018671",
    "nando_id": "NANDO:1200930"
  },
  {
    "id": "C0026103",
    "id2": "MedGen UID:6399",
    "medgen_label": "IgG4-related dacryoadenitis and sialadenitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6399",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019191",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019191",
    "nando_id": "NANDO:1200929"
  },
  {
    "id": "C0265836",
    "id2": "MedGen UID:539527",
    "medgen_label": "Congenital tricuspid stenosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/539527",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0019813",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019813",
    "nando_id": "NANDO:1200962"
  },
  {
    "id": "C1096116",
    "id2": "MedGen UID:204253",
    "medgen_label": "Acquired hemophilia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/204253",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019139",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019139",
    "nando_id": "NANDO:1200898"
  },
  {
    "id": "C1260899",
    "id2": "MedGen UID:266045",
    "medgen_label": "Diamond-Blackfan anemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/266045",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015253",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015253",
    "nando_id": "NANDO:1200890"
  },
  {
    "id": "C3203653",
    "id2": "MedGen UID:473761",
    "medgen_label": "IgG4-related disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/473761",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0017287",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017287",
    "nando_id": "NANDO:1200924"
  },
  {
    "id": "C3203653",
    "id2": "MedGen UID:473761",
    "medgen_label": "IgG4-related disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/473761",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017287",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017287",
    "nando_id": "NANDO:1200923"
  },
  {
    "id": "C4302109",
    "id2": "MedGen UID:927778",
    "medgen_label": "IgG4-related sclerosing cholangitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/927778",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018645",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018645",
    "nando_id": "NANDO:1200928"
  },
  {
    "id": "C4707560",
    "id2": "MedGen UID:1647585",
    "medgen_label": "Adult pure red cell aplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1647585",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020338",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020338",
    "nando_id": "NANDO:1200889"
  },
  {
    "id": "C0085280",
    "id2": "MedGen UID:39014",
    "medgen_label": "Arteriohepatic dysplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/39014",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007318",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007318",
    "nando_id": "NANDO:1200918"
  },
  {
    "id": "C0085280",
    "id2": "MedGen UID:39014",
    "medgen_label": "Arteriohepatic dysplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/39014",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0007318",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007318",
    "nando_id": "NANDO:1200919"
  },
  {
    "id": "C0339427",
    "id2": "MedGen UID:573145",
    "medgen_label": "Partial central choroid dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/573145",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0004890",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004890",
    "nando_id": "NANDO:1200939"
  },
  {
    "id": "C0339508",
    "id2": "MedGen UID:137919",
    "medgen_label": "Hereditary macular dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/137919",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020242",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020242",
    "nando_id": "NANDO:1200931"
  },
  {
    "id": "C0345217",
    "id2": "MedGen UID:83377",
    "medgen_label": "Cloacal exstrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/83377",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009774",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009774",
    "nando_id": "NANDO:1200910"
  },
  {
    "id": "C0345217",
    "id2": "MedGen UID:83377",
    "medgen_label": "Cloacal exstrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/83377",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009774",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009774",
    "nando_id": "NANDO:1200909"
  },
  {
    "id": "C0272362",
    "id2": "MedGen UID:543999",
    "medgen_label": "Acquired von willebrand syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/543999",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020460",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020460",
    "nando_id": "NANDO:1200899"
  },
  {
    "id": "C0282207",
    "id2": "MedGen UID:129128",
    "medgen_label": "Cronkhite-Canada syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/129128",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008283",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008283",
    "nando_id": "NANDO:1200901"
  },
  {
    "id": "C0015625",
    "id2": "MedGen UID:41967",
    "medgen_label": "Fanconi anemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/41967",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019391",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019391",
    "nando_id": "NANDO:1200891"
  },
  {
    "id": "C0019569",
    "id2": "MedGen UID:5559",
    "medgen_label": "Aganglionic megacolon",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5559",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018309",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018309",
    "nando_id": "NANDO:1200903"
  },
  {
    "id": "C0235833",
    "id2": "MedGen UID:68625",
    "medgen_label": "Congenital diaphragmatic hernia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/68625",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005711",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005711",
    "nando_id": "NANDO:1200911"
  },
  {
    "id": "C0238120",
    "id2": "MedGen UID:1393253",
    "medgen_label": "Acquired factor XIII deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1393253",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0021133",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0021133",
    "nando_id": "NANDO:1200897"
  },
  {
    "id": "C0238339",
    "id2": "MedGen UID:116056",
    "medgen_label": "Hereditary pancreatitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/116056",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008185",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008185",
    "nando_id": "NANDO:1200921"
  },
  {
    "id": "C0243002",
    "id2": "MedGen UID:67034",
    "medgen_label": "Tricuspid atresia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/67034",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0011514",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011514",
    "nando_id": "NANDO:1200962"
  },
  {
    "id": "C1568247",
    "id2": "MedGen UID:292820",
    "medgen_label": "Usher syndrome type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/292820",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010168",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010168",
    "nando_id": "NANDO:1200942"
  },
  {
    "id": "C1568248",
    "id2": "MedGen UID:339336",
    "medgen_label": "Usher syndrome type 3",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/339336",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016485",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016485",
    "nando_id": "NANDO:1200944"
  },
  {
    "id": "C1829703",
    "id2": "MedGen UID:316820",
    "medgen_label": "Carnitine palmitoyl transferase 1A deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/316820",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009705",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009705",
    "nando_id": "NANDO:1200970"
  },
  {
    "id": "C0158618",
    "id2": "MedGen UID:57857",
    "medgen_label": "Congenital mitral stenosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/57857",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020398",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020398",
    "nando_id": "NANDO:1200963"
  },
  {
    "id": "C0175694",
    "id2": "MedGen UID:61231",
    "medgen_label": "Smith-Lemli-Opitz syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/61231",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010035",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010035",
    "nando_id": "NANDO:1200961"
  },
  {
    "id": "C0206307",
    "id2": "MedGen UID:61565",
    "medgen_label": "Spongy degeneration of central nervous system",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/61565",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010079",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010079",
    "nando_id": "NANDO:1200948"
  },
  {
    "id": "C3150833",
    "id2": "MedGen UID:462183",
    "medgen_label": "Occult macular dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/462183",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013316",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013316",
    "nando_id": "NANDO:1200934"
  },
  {
    "id": "C0026269",
    "id2": "MedGen UID:44466",
    "medgen_label": "Mitral stenosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44466",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005852",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005852",
    "nando_id": "NANDO:1200963"
  },
  {
    "id": "C0027341",
    "id2": "MedGen UID:10257",
    "medgen_label": "Nail-patella syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10257",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008061",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008061",
    "nando_id": "NANDO:1200967"
  },
  {
    "id": "C0270972",
    "id2": "MedGen UID:78752",
    "medgen_label": "De Lange syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78752",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016033",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016033",
    "nando_id": "NANDO:1200960"
  },
  {
    "id": "C0271093",
    "id2": "MedGen UID:75734",
    "medgen_label": "Stargardt disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75734",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019353",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019353",
    "nando_id": "NANDO:1200933"
  },
  {
    "id": "C0271097",
    "id2": "MedGen UID:78754",
    "medgen_label": "Usher syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78754",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019501",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019501",
    "nando_id": "NANDO:1200941"
  },
  {
    "id": "C0917796",
    "id2": "MedGen UID:182973",
    "medgen_label": "Leber optic atrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/182973",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010788",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010788",
    "nando_id": "NANDO:1200940"
  },
  {
    "id": "C1858854",
    "id2": "MedGen UID:347006",
    "medgen_label": "Megalencephalic leukoencephalopathy with subcortical cysts",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/347006",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011391",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011391",
    "nando_id": "NANDO:1200950"
  },
  {
    "id": "C3714753",
    "id2": "MedGen UID:811458",
    "medgen_label": "Juvenile retinoschisis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/811458",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010725",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010725",
    "nando_id": "NANDO:1200938"
  },
  {
    "id": "C4085590",
    "id2": "MedGen UID:896366",
    "medgen_label": "Cone-rod dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/896366",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015993",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015993",
    "nando_id": "NANDO:1200937"
  },
  {
    "id": "C4273988",
    "id2": "MedGen UID:908684",
    "medgen_label": "Benign adult familial myoclonic epilepsy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/908684",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019448",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019448",
    "nando_id": "NANDO:1200956"
  },
  {
    "id": "C4708598",
    "id2": "MedGen UID:1642329",
    "medgen_label": "Partial duplication of the long arm of chromosome 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1642329",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016952",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016952",
    "nando_id": "NANDO:1200958"
  },
  {
    "id": "C0339510",
    "id2": "MedGen UID:137920",
    "medgen_label": "Vitelliform macular dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/137920",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000390",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000390",
    "nando_id": "NANDO:1200932"
  },
  {
    "id": "C0339534",
    "id2": "MedGen UID:83288",
    "medgen_label": "Usher syndrome type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/83288",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016484",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016484",
    "nando_id": "NANDO:1200943"
  },
  {
    "id": "C0342790",
    "id2": "MedGen UID:137978",
    "medgen_label": "Carnitine palmitoyltransferase II deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/137978",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015515",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015515",
    "nando_id": "NANDO:1200971"
  },
  {
    "id": "C0730290",
    "id2": "MedGen UID:676499",
    "medgen_label": "Cone dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/676499",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000455",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000455",
    "nando_id": "NANDO:1200936"
  },
  {
    "id": "C4014588",
    "id2": "MedGen UID:863025",
    "medgen_label": "Leukoencephalopathy, progressive, with ovarian failure",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/863025",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014387",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014387",
    "nando_id": "NANDO:1200952"
  },
  {
    "id": "C4551771",
    "id2": "MedGen UID:1684615",
    "medgen_label": "Kleefstra syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1684615",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012455",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012455",
    "nando_id": "NANDO:1200959"
  },
  {
    "id": "C0751778",
    "id2": "MedGen UID:199732",
    "medgen_label": "Progressive myoclonic epilepsy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/199732",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020074",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020074",
    "nando_id": "NANDO:1200953"
  },
  {
    "id": "C0751783",
    "id2": "MedGen UID:155631",
    "medgen_label": "Lafora disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155631",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009697",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009697",
    "nando_id": "NANDO:1200955"
  },
  {
    "id": "C0751785",
    "id2": "MedGen UID:155923",
    "medgen_label": "Unverricht-Lundborg syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155923",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009698",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009698",
    "nando_id": "NANDO:1200954"
  },
  {
    "id": "C1536451",
    "id2": "MedGen UID:283932",
    "medgen_label": "Central areolar choroidal dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/283932",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008982",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008982",
    "nando_id": "NANDO:1200939"
  },
  {
    "id": "C5680865",
    "id2": "MedGen UID:1826176",
    "medgen_label": "Congenital pulmonary veins atresia or stenosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1826176",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017864",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017864",
    "nando_id": "NANDO:1200964"
  },
  {
    "id": "C5681080",
    "id2": "MedGen UID:1842227",
    "medgen_label": "Disorder of carnitine cycle and carnitine transport",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1842227",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017716",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017716",
    "nando_id": "NANDO:1200969"
  },
  {
    "id": "C1622345",
    "id2": "MedGen UID:301243",
    "medgen_label": "Finnish type amyloidosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/301243",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007097",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007097",
    "nando_id": "NANDO:1201063"
  },
  {
    "id": "C1848561",
    "id2": "MedGen UID:341256",
    "medgen_label": "Cobalamin C disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/341256",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010184",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010184",
    "nando_id": "NANDO:1201040"
  },
  {
    "id": "C1849453",
    "id2": "MedGen UID:336602",
    "medgen_label": "Rapadilino syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/336602",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009955",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009955",
    "nando_id": "NANDO:1201058"
  },
  {
    "id": "C1853942",
    "id2": "MedGen UID:340091",
    "medgen_label": "Neonatal intrahepatic cholestasis due to citrin deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/340091",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011601",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011601",
    "nando_id": "NANDO:1200979"
  },
  {
    "id": "C0003076",
    "id2": "MedGen UID:1941",
    "medgen_label": "Congenital aniridia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1941",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019172",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019172",
    "nando_id": "NANDO:1201001"
  },
  {
    "id": "C0010674",
    "id2": "MedGen UID:41393",
    "medgen_label": "Cystic fibrosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/41393",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009061",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009061",
    "nando_id": "NANDO:1201021"
  },
  {
    "id": "C0206138",
    "id2": "MedGen UID:60083",
    "medgen_label": "CREST syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/60083",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0019563",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019563",
    "nando_id": "NANDO:1201011"
  },
  {
    "id": "C0206245",
    "id2": "MedGen UID:104815",
    "medgen_label": "Familial amyloid neuropathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/104815",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0007100",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007100",
    "nando_id": "NANDO:1201060"
  },
  {
    "id": "C1997910",
    "id2": "MedGen UID:372684",
    "medgen_label": "Citrin deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/372684",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016602",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016602",
    "nando_id": "NANDO:1200978"
  },
  {
    "id": "C2675179",
    "id2": "MedGen UID:436367",
    "medgen_label": "Arginine:glycine amidinotransferase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/436367",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012996",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012996",
    "nando_id": "NANDO:1201033"
  },
  {
    "id": "C5244016",
    "id2": "MedGen UID:1826001",
    "medgen_label": "Cerebral creatine deficiency syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1826001",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000456",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000456",
    "nando_id": "NANDO:1201032"
  },
  {
    "id": "C0029294",
    "id2": "MedGen UID:14518",
    "medgen_label": "Orofaciodigital syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/14518",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015375",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015375",
    "nando_id": "NANDO:1201051"
  },
  {
    "id": "C0029454",
    "id2": "MedGen UID:18223",
    "medgen_label": "Osteopetrosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/18223",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017198",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017198",
    "nando_id": "NANDO:1200998"
  },
  {
    "id": "C0268312",
    "id2": "MedGen UID:75668",
    "medgen_label": "Progressive familial intrahepatic cholestasis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75668",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015762",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015762",
    "nando_id": "NANDO:1201042"
  },
  {
    "id": "C0268468",
    "id2": "MedGen UID:120642",
    "medgen_label": "Dopa-responsive dystonia due to sepiapterin reductase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120642",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012994",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012994",
    "nando_id": "NANDO:1200982"
  },
  {
    "id": "C0393591",
    "id2": "MedGen UID:97953",
    "medgen_label": "Aicardi Goutieres syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/97953",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018866",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018866",
    "nando_id": "NANDO:1200996"
  },
  {
    "id": "C0393929",
    "id2": "MedGen UID:140751",
    "medgen_label": "Familial infantile myasthenia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/140751",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009689",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009689",
    "nando_id": "NANDO:1201057"
  },
  {
    "id": "C0396051",
    "id2": "MedGen UID:97973",
    "medgen_label": "Congenital subglottic stenosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/97973",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015395",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015395",
    "nando_id": "NANDO:1201004"
  },
  {
    "id": "C0403553",
    "id2": "MedGen UID:96045",
    "medgen_label": "Renal dysplasia and retinal aplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/96045",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017842",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017842",
    "nando_id": "NANDO:1201049"
  },
  {
    "id": "C1855681",
    "id2": "MedGen UID:343406",
    "medgen_label": "Nephronophthisis 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/343406",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009728",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009728",
    "nando_id": "NANDO:1201036"
  },
  {
    "id": "C1856061",
    "id2": "MedGen UID:343470",
    "medgen_label": "Homocystinuria due to methylene tetrahydrofolate reductase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/343470",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009353",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009353",
    "nando_id": "NANDO:1201041"
  },
  {
    "id": "C1862839",
    "id2": "MedGen UID:350766",
    "medgen_label": "Anterior segment dysgenesis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/350766",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019503",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019503",
    "nando_id": "NANDO:1201000"
  },
  {
    "id": "C3489789",
    "id2": "MedGen UID:483742",
    "medgen_label": "Progressive familial intrahepatic cholestasis type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/483742",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011156",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011156",
    "nando_id": "NANDO:1201044"
  },
  {
    "id": "C3495801",
    "id2": "MedGen UID:811223",
    "medgen_label": "Granulomatosis with polyangiitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/811223",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0012105",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012105",
    "nando_id": "NANDO:1201009"
  },
  {
    "id": "C3696376",
    "id2": "MedGen UID:777186",
    "medgen_label": "3-Methylglutaconic aciduria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/777186",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017359",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017359",
    "nando_id": "NANDO:1200989"
  },
  {
    "id": "C5201145",
    "id2": "MedGen UID:1684821",
    "medgen_label": "Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1684821",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012465",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012465",
    "nando_id": "NANDO:1200983"
  },
  {
    "id": "C0339273",
    "id2": "MedGen UID:90939",
    "medgen_label": "Gelatinous droplike corneal dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/90939",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008777",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008777",
    "nando_id": "NANDO:1201006"
  },
  {
    "id": "C0342727",
    "id2": "MedGen UID:90994",
    "medgen_label": "3-methylglutaconic aciduria type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/90994",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009610",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009610",
    "nando_id": "NANDO:1200990"
  },
  {
    "id": "C0342788",
    "id2": "MedGen UID:90999",
    "medgen_label": "Renal carnitine transport defect",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/90999",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008919",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008919",
    "nando_id": "NANDO:1200973"
  },
  {
    "id": "C0342791",
    "id2": "MedGen UID:91000",
    "medgen_label": "Carnitine acylcarnitine translocase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/91000",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008918",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008918",
    "nando_id": "NANDO:1200972"
  },
  {
    "id": "C0687120",
    "id2": "MedGen UID:146912",
    "medgen_label": "Nephronophthisis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/146912",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019005",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019005",
    "nando_id": "NANDO:1201036"
  },
  {
    "id": "C0748540",
    "id2": "MedGen UID:148187",
    "medgen_label": "Limited cutaneous systemic sclerosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/148187",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016358",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016358",
    "nando_id": "NANDO:1201011"
  },
  {
    "id": "C1845862",
    "id2": "MedGen UID:337451",
    "medgen_label": "Creatine transporter deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/337451",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010305",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010305",
    "nando_id": "NANDO:1201035"
  },
  {
    "id": "C3887654",
    "id2": "MedGen UID:854497",
    "medgen_label": "Vasculitis due to ADA2 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/854497",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014306",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014306",
    "nando_id": "NANDO:1200995"
  },
  {
    "id": "C4015067",
    "id2": "MedGen UID:863504",
    "medgen_label": "Periodic fever-infantile enterocolitis-autoinflammatory syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/863504",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014472",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014472",
    "nando_id": "NANDO:1200994"
  },
  {
    "id": "C4551990",
    "id2": "MedGen UID:1639219",
    "medgen_label": "Familial hypobetalipoproteinemia 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1639219",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014252",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014252",
    "nando_id": "NANDO:1201037"
  },
  {
    "id": "C5548200",
    "id2": "MedGen UID:1785446",
    "medgen_label": "Neonatal glycine encephalopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1785446",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017353",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017353",
    "nando_id": "NANDO:1200985"
  },
  {
    "id": "C5548209",
    "id2": "MedGen UID:1781124",
    "medgen_label": "Infantile glycine encephalopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1781124",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017354",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017354",
    "nando_id": "NANDO:1200986"
  },
  {
    "id": "C0033300",
    "id2": "MedGen UID:46123",
    "medgen_label": "Hutchinson-Gilford syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/46123",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008310",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008310",
    "nando_id": "NANDO:1201007"
  },
  {
    "id": "C0272328",
    "id2": "MedGen UID:543977",
    "medgen_label": "Acquired factor X deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/543977",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0021134",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0021134",
    "nando_id": "NANDO:1201048"
  },
  {
    "id": "C1863844",
    "id2": "MedGen UID:350276",
    "medgen_label": "Citrullinemia type II",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/350276",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016603",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016603",
    "nando_id": "NANDO:1200980"
  },
  {
    "id": "C1864233",
    "id2": "MedGen UID:400481",
    "medgen_label": "Congenital myasthenic syndrome 5",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/400481",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011281",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011281",
    "nando_id": "NANDO:1201056"
  },
  {
    "id": "C1865643",
    "id2": "MedGen UID:356333",
    "medgen_label": "Progressive familial intrahepatic cholestasis type 3",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/356333",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011214",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011214",
    "nando_id": "NANDO:1201045"
  },
  {
    "id": "C1969443",
    "id2": "MedGen UID:370665",
    "medgen_label": "Mitochondrial trifunctional protein deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/370665",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012172",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012172",
    "nando_id": "NANDO:1200974"
  },
  {
    "id": "C2931067",
    "id2": "MedGen UID:418976",
    "medgen_label": "Cholestasis, progressive familial intrahepatic, 4",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/418976",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014381",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014381",
    "nando_id": "NANDO:1201046"
  },
  {
    "id": "C4310747",
    "id2": "MedGen UID:934714",
    "medgen_label": "Cholestasis, progressive familial intrahepatic, 5",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/934714",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014884",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014884",
    "nando_id": "NANDO:1201047"
  },
  {
    "id": "C0017920",
    "id2": "MedGen UID:6640",
    "medgen_label": "Glycogen storage disease, type I",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6640",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002413",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002413",
    "nando_id": "NANDO:1201018"
  },
  {
    "id": "C0017922",
    "id2": "MedGen UID:6641",
    "medgen_label": "Glycogen storage disease type III",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6641",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009291",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009291",
    "nando_id": "NANDO:1201019"
  },
  {
    "id": "C0019880",
    "id2": "MedGen UID:42485",
    "medgen_label": "Homocystinuria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/42485",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0004737",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004737",
    "nando_id": "NANDO:1201038"
  },
  {
    "id": "C0265308",
    "id2": "MedGen UID:120532",
    "medgen_label": "Baller-Gerold syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120532",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009039",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009039",
    "nando_id": "NANDO:1201059"
  },
  {
    "id": "C0265767",
    "id2": "MedGen UID:120556",
    "medgen_label": "Congenital tracheal stenosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120556",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011340",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011340",
    "nando_id": "NANDO:1201003"
  },
  {
    "id": "C0574080",
    "id2": "MedGen UID:154356",
    "medgen_label": "Deficiency of guanidinoacetate methyltransferase",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/154356",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012999",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012999",
    "nando_id": "NANDO:1201034"
  },
  {
    "id": "C0574083",
    "id2": "MedGen UID:107893",
    "medgen_label": "3-Methylglutaconic aciduria type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/107893",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010543",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010543",
    "nando_id": "NANDO:1200991"
  },
  {
    "id": "C0574084",
    "id2": "MedGen UID:108273",
    "medgen_label": "3-Methylglutaconic aciduria type 3",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/108273",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009787",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009787",
    "nando_id": "NANDO:1200992"
  },
  {
    "id": "C0751202",
    "id2": "MedGen UID:199606",
    "medgen_label": "Classic homocystinuria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/199606",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009352",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009352",
    "nando_id": "NANDO:1201039"
  },
  {
    "id": "C0751748",
    "id2": "MedGen UID:155625",
    "medgen_label": "Non-ketotic hyperglycinemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155625",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011612",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011612",
    "nando_id": "NANDO:1200984"
  },
  {
    "id": "C1291564",
    "id2": "MedGen UID:220945",
    "medgen_label": "Deficiency of aromatic-L-amino-acid decarboxylase",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/220945",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012084",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012084",
    "nando_id": "NANDO:1200988"
  },
  {
    "id": "C1536500",
    "id2": "MedGen UID:280689",
    "medgen_label": "Deficiency of acetyl-CoA acetyltransferase",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/280689",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008760",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008760",
    "nando_id": "NANDO:1200987"
  },
  {
    "id": "C5680269",
    "id2": "MedGen UID:1842920",
    "medgen_label": "AApoAI amyloidosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1842920",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019731",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019731",
    "nando_id": "NANDO:1201062"
  },
  {
    "id": "CN282059",
    "id2": "MedGen UID:965566",
    "medgen_label": "Diffuse cutaneous systemic sclerosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/965566",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016356",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016356",
    "nando_id": "NANDO:1201010"
  },
  {
    "id": "CN294825",
    "id2": "MedGen UID:978099",
    "medgen_label": "A20 haploinsufficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/978099",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0100222",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0100222",
    "nando_id": "NANDO:1200997"
  },
  {
    "id": "CN295299",
    "id2": "MedGen UID:976464",
    "medgen_label": "Citrullinemia, type II, adult-onset",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/976464",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0011326",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011326",
    "nando_id": "NANDO:1200980"
  },
  {
    "id": "C2932717",
    "id2": "MedGen UID:444371",
    "medgen_label": "Pseudohypoparathyroidism type II",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/444371",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008749",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008749",
    "nando_id": "NANDO:1201078"
  },
  {
    "id": "C3159322",
    "id2": "MedGen UID:463613",
    "medgen_label": "Spondyloepimetaphyseal dysplasia, Maroteaux type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/463613",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008473",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008473",
    "nando_id": "NANDO:1201100"
  },
  {
    "id": "CN030853",
    "id2": "MedGen UID:1841549",
    "medgen_label": "Ehlers-Danlos syndrome progeroid type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1841549",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007526",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007526",
    "nando_id": "NANDO:1201088"
  },
  {
    "id": "C0023418",
    "id2": "MedGen UID:9725",
    "medgen_label": "Leukemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9725",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005059",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005059",
    "nando_id": "NANDO:2100002"
  },
  {
    "id": "C0024299",
    "id2": "MedGen UID:44223",
    "medgen_label": "Lymphoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44223",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005062",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005062",
    "nando_id": "NANDO:2100004"
  },
  {
    "id": "C0027726",
    "id2": "MedGen UID:10308",
    "medgen_label": "Nephrotic syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10308",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005377",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005377",
    "nando_id": "NANDO:2100009"
  },
  {
    "id": "C0266464",
    "id2": "MedGen UID:78605",
    "medgen_label": "Polymicrogyria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78605",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000087",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000087",
    "nando_id": "NANDO:1201071"
  },
  {
    "id": "C0268347",
    "id2": "MedGen UID:82791",
    "medgen_label": "Ehlers-Danlos syndrome, periodontitis type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82791",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007527",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007527",
    "nando_id": "NANDO:1201091"
  },
  {
    "id": "C0348374",
    "id2": "MedGen UID:87593",
    "medgen_label": "Malignant neoplasm of the central nervous system",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/87593",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002714",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002714",
    "nando_id": "NANDO:2100007"
  },
  {
    "id": "C0432227",
    "id2": "MedGen UID:96583",
    "medgen_label": "Brachyrachia (short spine dysplasia)",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/96583",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0007232",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007232",
    "nando_id": "NANDO:1201102"
  },
  {
    "id": "C3494506",
    "id2": "MedGen UID:488447",
    "medgen_label": "Pseudohypoparathyroidism type I A",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/488447",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007078",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007078",
    "nando_id": "NANDO:1201075"
  },
  {
    "id": "C0042514",
    "id2": "MedGen UID:12068",
    "medgen_label": "Ventricular tachycardia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/12068",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005477",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005477",
    "nando_id": "NANDO:2100049"
  },
  {
    "id": "C4303789",
    "id2": "MedGen UID:929458",
    "medgen_label": "Ehlers-Danlos syndrome, cardiac valvular type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/929458",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009159",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009159",
    "nando_id": "NANDO:1201086"
  },
  {
    "id": "C0019618",
    "id2": "MedGen UID:6845",
    "medgen_label": "Histiocytosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6845",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002637",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002637",
    "nando_id": "NANDO:2100005"
  },
  {
    "id": "C0242666",
    "id2": "MedGen UID:69229",
    "medgen_label": "Protein S deficiency disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/69229",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002304",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002304",
    "nando_id": "NANDO:1201081"
  },
  {
    "id": "C0265280",
    "id2": "MedGen UID:82698",
    "medgen_label": "Spondylometaphyseal dysplasia, Kozlowski type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82698",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008477",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008477",
    "nando_id": "NANDO:1201101"
  },
  {
    "id": "C0265281",
    "id2": "MedGen UID:82699",
    "medgen_label": "Metatropic dysplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82699",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007986",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007986",
    "nando_id": "NANDO:1201099"
  },
  {
    "id": "C1332206",
    "id2": "MedGen UID:233965",
    "medgen_label": "Adult lymphoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/233965",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0003660",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003660",
    "nando_id": "NANDO:2100004"
  },
  {
    "id": "C1332977",
    "id2": "MedGen UID:234132",
    "medgen_label": "Childhood leukemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/234132",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0004355",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004355",
    "nando_id": "NANDO:2100002"
  },
  {
    "id": "C1332979",
    "id2": "MedGen UID:232062",
    "medgen_label": "Pediatric lymphoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/232062",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0003659",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003659",
    "nando_id": "NANDO:2100004"
  },
  {
    "id": "C1846058",
    "id2": "MedGen UID:337496",
    "medgen_label": "Syndromic X-linked intellectual disability Lubs type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/337496",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0010283",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010283",
    "nando_id": "NANDO:1201095"
  },
  {
    "id": "C1847406",
    "id2": "MedGen UID:335678",
    "medgen_label": "Familial digital arthropathy-brachydactyly",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/335678",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011732",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011732",
    "nando_id": "NANDO:1201103"
  },
  {
    "id": "C1848201",
    "id2": "MedGen UID:336288",
    "medgen_label": "Subcortical band heterotopia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/336288",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020491",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020491",
    "nando_id": "NANDO:1201070"
  },
  {
    "id": "C0008780",
    "id2": "MedGen UID:3467",
    "medgen_label": "Primary ciliary dyskinesia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/3467",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0016575",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016575",
    "nando_id": "NANDO:1201097"
  },
  {
    "id": "C0008780",
    "id2": "MedGen UID:3467",
    "medgen_label": "Primary ciliary dyskinesia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/3467",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016575",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016575",
    "nando_id": "NANDO:1201096"
  },
  {
    "id": "C0431375",
    "id2": "MedGen UID:98463",
    "medgen_label": "Classic lissencephaly",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/98463",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0015146",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015146",
    "nando_id": "NANDO:1201068"
  },
  {
    "id": "C0431375",
    "id2": "MedGen UID:98463",
    "medgen_label": "Classic lissencephaly",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/98463",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0015146",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015146",
    "nando_id": "NANDO:1201069"
  },
  {
    "id": "C0431376",
    "id2": "MedGen UID:96562",
    "medgen_label": "Cobblestone lissencephaly",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/96562",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018869",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018869",
    "nando_id": "NANDO:1201072"
  },
  {
    "id": "C2932716",
    "id2": "MedGen UID:420958",
    "medgen_label": "Pseudohypoparathyroidism type 1C",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/420958",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012911",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012911",
    "nando_id": "NANDO:1201077"
  },
  {
    "id": "C5243927",
    "id2": "MedGen UID:1800807",
    "medgen_label": "Acid sphingomyelinase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1800807",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0100464",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0100464",
    "nando_id": "NANDO:1201084"
  },
  {
    "id": "C0022661",
    "id2": "MedGen UID:9637",
    "medgen_label": "Chronic renal failure syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9637",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0024327",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0024327",
    "nando_id": "NANDO:2100023"
  },
  {
    "id": "C0266484",
    "id2": "MedGen UID:78606",
    "medgen_label": "Schizencephaly",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78606",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010011",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010011",
    "nando_id": "NANDO:1201073"
  },
  {
    "id": "C0268374",
    "id2": "MedGen UID:82798",
    "medgen_label": "Junctional epidermolysis bullosa, non-Herlitz type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82798",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009180",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009180",
    "nando_id": "NANDO:1201066"
  },
  {
    "id": "C4082173",
    "id2": "MedGen UID:901502",
    "medgen_label": "Porencephaly",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/901502",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017410",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017410",
    "nando_id": "NANDO:1201074"
  },
  {
    "id": "C4225313",
    "id2": "MedGen UID:907426",
    "medgen_label": "Bethlem myopathy 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/907426",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0034022",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0034022",
    "nando_id": "NANDO:1201090"
  },
  {
    "id": "C4693870",
    "id2": "MedGen UID:1632001",
    "medgen_label": "Ehlers-Danlos syndrome, classic-like, 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1632001",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0054813",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0054813",
    "nando_id": "NANDO:1201085"
  },
  {
    "id": "C0079683",
    "id2": "MedGen UID:36328",
    "medgen_label": "Junctional epidermolysis bullosa gravis of Herlitz",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/36328",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009182",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009182",
    "nando_id": "NANDO:1201065"
  },
  {
    "id": "C0598221",
    "id2": "MedGen UID:671121",
    "medgen_label": "Hereditary thrombophilia due to congenital protein C deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/671121",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019145",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019145",
    "nando_id": "NANDO:1201080"
  },
  {
    "id": "C1838657",
    "id2": "MedGen UID:374020",
    "medgen_label": "Vitamin D hydroxylation-deficient rickets, type 1B",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/374020",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010810",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010810",
    "nando_id": "NANDO:1201093"
  },
  {
    "id": "C1864100",
    "id2": "MedGen UID:350343",
    "medgen_label": "Pseudohypoparathyroidism type 1B",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/350343",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011301",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011301",
    "nando_id": "NANDO:1201076"
  },
  {
    "id": "C1866294",
    "id2": "MedGen UID:356497",
    "medgen_label": "Ehlers-Danlos syndrome, musculocontractural type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/356497",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011142",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011142",
    "nando_id": "NANDO:1201089"
  },
  {
    "id": "C1868720",
    "id2": "MedGen UID:358387",
    "medgen_label": "Periventricular nodular heterotopia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/358387",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020341",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020341",
    "nando_id": "NANDO:1201079"
  },
  {
    "id": "C5436733",
    "id2": "MedGen UID:1725534",
    "medgen_label": "Vitamin D-dependent rickets, type 3",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1725534",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0033640",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0033640",
    "nando_id": "NANDO:1201094"
  },
  {
    "id": "C0022541",
    "id2": "MedGen UID:9618",
    "medgen_label": "Kearns-Sayre syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9618",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010787",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010787",
    "nando_id": "NANDO:1201064"
  },
  {
    "id": "C0265219",
    "id2": "MedGen UID:78538",
    "medgen_label": "Miller Dieker syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78538",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009532",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009532",
    "nando_id": "NANDO:1201083"
  },
  {
    "id": "C5680977",
    "id2": "MedGen UID:1842686",
    "medgen_label": "TRPV4-related bone disorder",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1842686",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018240",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018240",
    "nando_id": "NANDO:1201098"
  },
  {
    "id": "CN263128",
    "id2": "MedGen UID:946156",
    "medgen_label": "Brittle cornea syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/946156",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009242",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009242",
    "nando_id": "NANDO:1201087"
  },
  {
    "id": "CN283242",
    "id2": "MedGen UID:968221",
    "medgen_label": "Vitamin D-dependent rickets, type 1A",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/968221",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020723",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020723",
    "nando_id": "NANDO:1201092"
  },
  {
    "id": "C0002880",
    "id2": "MedGen UID:1918",
    "medgen_label": "Autoimmune hemolytic anemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1918",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020108",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020108",
    "nando_id": "NANDO:2100181"
  },
  {
    "id": "C0002881",
    "id2": "MedGen UID:1919",
    "medgen_label": "Familial hemolytic anemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1919",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0003689",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003689",
    "nando_id": "NANDO:2100183"
  },
  {
    "id": "C0007001",
    "id2": "MedGen UID:2825",
    "medgen_label": "Inborn carbohydrate metabolic disorder",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/2825",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019214",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019214",
    "nando_id": "NANDO:2100164"
  },
  {
    "id": "C0009326",
    "id2": "MedGen UID:3157",
    "medgen_label": "Rheumatic disorder",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/3157",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005554",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005554",
    "nando_id": "NANDO:2100151"
  },
  {
    "id": "C0009782",
    "id2": "MedGen UID:1098",
    "medgen_label": "Connective tissue disorder",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1098",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0003900",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003900",
    "nando_id": "NANDO:2100172"
  },
  {
    "id": "C0011848",
    "id2": "MedGen UID:8349",
    "medgen_label": "Diabetes insipidus",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/8349",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0004782",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004782",
    "nando_id": "NANDO:2100117"
  },
  {
    "id": "C0011849",
    "id2": "MedGen UID:8350",
    "medgen_label": "Diabetes mellitus",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/8350",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005015",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005015",
    "nando_id": "NANDO:2100157"
  },
  {
    "id": "C0025521",
    "id2": "MedGen UID:6323",
    "medgen_label": "Inborn errors of metabolism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6323",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019052",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019052",
    "nando_id": "NANDO:2100159"
  },
  {
    "id": "C0027662",
    "id2": "MedGen UID:45036",
    "medgen_label": "Multiple endocrine neoplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/45036",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017169",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017169",
    "nando_id": "NANDO:2100148"
  },
  {
    "id": "C0027868",
    "id2": "MedGen UID:10323",
    "medgen_label": "Neuromuscular disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10323",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019056",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019056",
    "nando_id": "NANDO:2100214"
  },
  {
    "id": "C0268634",
    "id2": "MedGen UID:468968",
    "medgen_label": "Disorder of fatty acid metabolism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/468968",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0037858",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0037858",
    "nando_id": "NANDO:2100162"
  },
  {
    "id": "C0398686",
    "id2": "MedGen UID:585013",
    "medgen_label": "Inborn error of immunity",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/585013",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0003778",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003778",
    "nando_id": "NANDO:2100204"
  },
  {
    "id": "C1263739",
    "id2": "MedGen UID:468982",
    "medgen_label": "Disorder of organic acid metabolism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/468982",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0045022",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0045022",
    "nando_id": "NANDO:2100161"
  },
  {
    "id": "C0085078",
    "id2": "MedGen UID:43098",
    "medgen_label": "Lysosomal storage disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/43098",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002561",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002561",
    "nando_id": "NANDO:2100165"
  },
  {
    "id": "C0085215",
    "id2": "MedGen UID:38820",
    "medgen_label": "Premature ovarian failure",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/38820",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005387",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005387",
    "nando_id": "NANDO:2100139"
  },
  {
    "id": "C0085409",
    "id2": "MedGen UID:39042",
    "medgen_label": "Autoimmune polyendocrinopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/39042",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017278",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017278",
    "nando_id": "NANDO:2100125"
  },
  {
    "id": "C0149670",
    "id2": "MedGen UID:472889",
    "medgen_label": "Carbohydrate metabolism disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/472889",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0037792",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0037792",
    "nando_id": "NANDO:2100164"
  },
  {
    "id": "C3890737",
    "id2": "MedGen UID:855741",
    "medgen_label": "Autoinflammatory syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/855741",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019751",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019751",
    "nando_id": "NANDO:2100156"
  },
  {
    "id": "C0034013",
    "id2": "MedGen UID:18752",
    "medgen_label": "Precocious puberty",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/18752",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000088",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000088",
    "nando_id": "NANDO:2100135"
  },
  {
    "id": "C0034902",
    "id2": "MedGen UID:11154",
    "medgen_label": "Pure red-cell aplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/11154",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001705",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001705",
    "nando_id": "NANDO:2100177"
  },
  {
    "id": "C0282528",
    "id2": "MedGen UID:129185",
    "medgen_label": "Peroxisomal disorder",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/129185",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019053",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019053",
    "nando_id": "NANDO:2100166"
  },
  {
    "id": "C2711630",
    "id2": "MedGen UID:751396",
    "medgen_label": "Combined immunodeficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/751396",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015131",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015131",
    "nando_id": "NANDO:2100203"
  },
  {
    "id": "C2930619",
    "id2": "MedGen UID:415936",
    "medgen_label": "Disorder of sexual differentiation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/415936",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002145",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002145",
    "nando_id": "NANDO:2100140"
  },
  {
    "id": "C0014130",
    "id2": "MedGen UID:4043",
    "medgen_label": "Disorder of endocrine system",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/4043",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005151",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005151",
    "nando_id": "NANDO:2100109"
  },
  {
    "id": "C0018817",
    "id2": "MedGen UID:6753",
    "medgen_label": "Atrial septal defect",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6753",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006664",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006664",
    "nando_id": "NANDO:2100085"
  },
  {
    "id": "C0018824",
    "id2": "MedGen UID:5463",
    "medgen_label": "cardiac valvular disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5463",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002869",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002869",
    "nando_id": "NANDO:2100105"
  },
  {
    "id": "C0018939",
    "id2": "MedGen UID:5483",
    "medgen_label": "Hematologic disorder",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5483",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005570",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005570",
    "nando_id": "NANDO:2100175"
  },
  {
    "id": "C0020635",
    "id2": "MedGen UID:9386",
    "medgen_label": "Hypopituitarism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9386",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005152",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005152",
    "nando_id": "NANDO:2100110"
  },
  {
    "id": "C0020676",
    "id2": "MedGen UID:6991",
    "medgen_label": "Hypothyroidism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6991",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005420",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005420",
    "nando_id": "NANDO:2100120"
  },
  {
    "id": "C0021051",
    "id2": "MedGen UID:7034",
    "medgen_label": "Immunodeficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7034",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0021094",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0021094",
    "nando_id": "NANDO:2100204"
  },
  {
    "id": "C0021053",
    "id2": "MedGen UID:5759",
    "medgen_label": "Immune system disorder",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5759",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005046",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005046",
    "nando_id": "NANDO:2100202"
  },
  {
    "id": "C0265316",
    "id2": "MedGen UID:82706",
    "medgen_label": "Neurocutaneous syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82706",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0042983",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0042983",
    "nando_id": "NANDO:2100220"
  },
  {
    "id": "C0751651",
    "id2": "MedGen UID:155901",
    "medgen_label": "Mitochondrial disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155901",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0044970",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0044970",
    "nando_id": "NANDO:2100163"
  },
  {
    "id": "C0857305",
    "id2": "MedGen UID:208992",
    "medgen_label": "Thrombocytopenic purpura",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/208992",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0043768",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0043768",
    "nando_id": "NANDO:2100188"
  },
  {
    "id": "C0857899",
    "id2": "MedGen UID:208996",
    "medgen_label": "Decreased circulating aldosterone concentration",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/208996",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015900",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015900",
    "nando_id": "NANDO:2100132"
  },
  {
    "id": "C1456275",
    "id2": "MedGen UID:1778113",
    "medgen_label": "Inborn mitochondrial metabolism disorder",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1778113",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0004069",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004069",
    "nando_id": "NANDO:2100163"
  },
  {
    "id": "CN199363",
    "id2": "MedGen UID:799481",
    "medgen_label": "Progeroid syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/799481",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015333",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015333",
    "nando_id": "NANDO:2100221"
  },
  {
    "id": "CN377664",
    "id2": "MedGen UID:1052972",
    "medgen_label": "Amino acid metabolism disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1052972",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0037871",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0037871",
    "nando_id": "NANDO:2100160"
  },
  {
    "id": "C0005940",
    "id2": "MedGen UID:14182",
    "medgen_label": "Disorder of bone",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/14182",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005381",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005381",
    "nando_id": "NANDO:2100291"
  },
  {
    "id": "C0008626",
    "id2": "MedGen UID:3441",
    "medgen_label": "Congenital chromosomal disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/3441",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019040",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019040",
    "nando_id": "NANDO:2100279"
  },
  {
    "id": "C0010278",
    "id2": "MedGen UID:1163",
    "medgen_label": "Craniosynostosis syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1163",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015469",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015469",
    "nando_id": "NANDO:2100227"
  },
  {
    "id": "C2931845",
    "id2": "MedGen UID:444156",
    "medgen_label": "Neurodegeneration with brain iron accumulation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/444156",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018307",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018307",
    "nando_id": "NANDO:2100241"
  },
  {
    "id": "C0023440",
    "id2": "MedGen UID:7316",
    "medgen_label": "Acute myeloid leukemia, M6 type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7316",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017858",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017858",
    "nando_id": "NANDO:2200010"
  },
  {
    "id": "C0023462",
    "id2": "MedGen UID:44124",
    "medgen_label": "Acute megakaryoblastic leukemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44124",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018872",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018872",
    "nando_id": "NANDO:2200011"
  },
  {
    "id": "C0023465",
    "id2": "MedGen UID:7319",
    "medgen_label": "Acute monocytic leukemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7319",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007896",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007896",
    "nando_id": "NANDO:2200009"
  },
  {
    "id": "C0023465",
    "id2": "MedGen UID:7319",
    "medgen_label": "Acute monocytic leukemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7319",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0007896",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007896",
    "nando_id": "NANDO:2200008"
  },
  {
    "id": "C0023487",
    "id2": "MedGen UID:44127",
    "medgen_label": "Acute promyelocytic leukemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44127",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012883",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012883",
    "nando_id": "NANDO:2200007"
  },
  {
    "id": "C0026998",
    "id2": "MedGen UID:10232",
    "medgen_label": "Acute myeloblastic leukemia without maturation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10232",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005224",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005224",
    "nando_id": "NANDO:2200005"
  },
  {
    "id": "C0349639",
    "id2": "MedGen UID:138109",
    "medgen_label": "Juvenile myelomonocytic leukemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/138109",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011908",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011908",
    "nando_id": "NANDO:2200015"
  },
  {
    "id": "C0349639",
    "id2": "MedGen UID:138109",
    "medgen_label": "Juvenile myelomonocytic leukemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/138109",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0011908",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011908",
    "nando_id": "NANDO:2200014"
  },
  {
    "id": "C0522631",
    "id2": "MedGen UID:101100",
    "medgen_label": "Acute myeloid leukemia with minimal differentiation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/101100",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005223",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005223",
    "nando_id": "NANDO:2200004"
  },
  {
    "id": "C1260325",
    "id2": "MedGen UID:220355",
    "medgen_label": "Follicular dendritic cell sarcoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/220355",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005764",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005764",
    "nando_id": "NANDO:2200034"
  },
  {
    "id": "C1260326",
    "id2": "MedGen UID:266040",
    "medgen_label": "Interdigitating dendritic cell sarcoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/266040",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005813",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005813",
    "nando_id": "NANDO:2200035"
  },
  {
    "id": "C3463824",
    "id2": "MedGen UID:483005",
    "medgen_label": "Myelodysplastic syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/483005",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018881",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018881",
    "nando_id": "NANDO:2200019"
  },
  {
    "id": "C3887558",
    "id2": "MedGen UID:854411",
    "medgen_label": "Hemophagocytic syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/854411",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015540",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015540",
    "nando_id": "NANDO:2200032"
  },
  {
    "id": "C3899655",
    "id2": "MedGen UID:859249",
    "medgen_label": "Langerhans cell histiocytosis specific to childhood",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/859249",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0017025",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017025",
    "nando_id": "NANDO:2200031"
  },
  {
    "id": "C3900100",
    "id2": "MedGen UID:859694",
    "medgen_label": "Langerhans cell histiocytosis specific to adulthood",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/859694",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0017029",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017029",
    "nando_id": "NANDO:2200031"
  },
  {
    "id": "C0037274",
    "id2": "MedGen UID:20777",
    "medgen_label": "Skin disorder",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/20777",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005093",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005093",
    "nando_id": "NANDO:2100281"
  },
  {
    "id": "C0042373",
    "id2": "MedGen UID:22621",
    "medgen_label": "Vascular disorder",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/22621",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005385",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005385",
    "nando_id": "NANDO:2100294"
  },
  {
    "id": "C0279543",
    "id2": "MedGen UID:75993",
    "medgen_label": "Chronic myelogenous leukemia, BCR-ABL1 positive",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75993",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011996",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011996",
    "nando_id": "NANDO:2200013"
  },
  {
    "id": "C0279584",
    "id2": "MedGen UID:83526",
    "medgen_label": "B-cell childhood acute lymphoblastic leukemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/83526",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000872",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000872",
    "nando_id": "NANDO:2200002"
  },
  {
    "id": "C0280634",
    "id2": "MedGen UID:128856",
    "medgen_label": "Adult acute monocytic leukemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/128856",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0000875",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000875",
    "nando_id": "NANDO:2200009"
  },
  {
    "id": "C0280634",
    "id2": "MedGen UID:128856",
    "medgen_label": "Adult acute monocytic leukemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/128856",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0000875",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000875",
    "nando_id": "NANDO:2200008"
  },
  {
    "id": "C0334108",
    "id2": "MedGen UID:137722",
    "medgen_label": "Polyposis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/137722",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000147",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000147",
    "nando_id": "NANDO:2100257"
  },
  {
    "id": "C1961099",
    "id2": "MedGen UID:368378",
    "medgen_label": "T-cell acute lymphoblastic leukemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/368378",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0004963",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004963",
    "nando_id": "NANDO:2200003"
  },
  {
    "id": "C0019621",
    "id2": "MedGen UID:5568",
    "medgen_label": "Langerhans cell histiocytosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5568",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018310",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018310",
    "nando_id": "NANDO:2200031"
  },
  {
    "id": "C0020981",
    "id2": "MedGen UID:7025",
    "medgen_label": "Angioimmunoblastic T-cell lymphoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7025",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0004977",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004977",
    "nando_id": "NANDO:2200029"
  },
  {
    "id": "C0021390",
    "id2": "MedGen UID:43877",
    "medgen_label": "Inflammatory bowel disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/43877",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005265",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005265",
    "nando_id": "NANDO:2100259"
  },
  {
    "id": "C0856562",
    "id2": "MedGen UID:797407",
    "medgen_label": "Inherited ichthyosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/797407",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015947",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015947",
    "nando_id": "NANDO:2100283"
  },
  {
    "id": "C1292777",
    "id2": "MedGen UID:266235",
    "medgen_label": "Aggressive NK-cell leukemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/266235",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019470",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019470",
    "nando_id": "NANDO:2200012"
  },
  {
    "id": "C1301357",
    "id2": "MedGen UID:226983",
    "medgen_label": "Acute leukemia of ambiguous lineage",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/226983",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0019460",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019460",
    "nando_id": "NANDO:2200017"
  },
  {
    "id": "C1301357",
    "id2": "MedGen UID:226983",
    "medgen_label": "Acute leukemia of ambiguous lineage",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/226983",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0019460",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019460",
    "nando_id": "NANDO:2200018"
  },
  {
    "id": "CN228979",
    "id2": "MedGen UID:833238",
    "medgen_label": "B-cell non-Hodgkin lymphoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/833238",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015759",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015759",
    "nando_id": "NANDO:2200020"
  },
  {
    "id": "CN294497",
    "id2": "MedGen UID:978369",
    "medgen_label": "Hodgkins lymphoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/978369",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0004952",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004952",
    "nando_id": "NANDO:2200024"
  },
  {
    "id": "CN377655",
    "id2": "MedGen UID:1052483",
    "medgen_label": "Peripheral T-cell lymphoma, not otherwise specified",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1052483",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0004964",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004964",
    "nando_id": "NANDO:2200028"
  },
  {
    "id": "C0158570",
    "id2": "MedGen UID:56387",
    "medgen_label": "Vascular malformation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/56387",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0024291",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0024291",
    "nando_id": "NANDO:2100295"
  },
  {
    "id": "C0206180",
    "id2": "MedGen UID:61533",
    "medgen_label": "Anaplastic large cell lymphoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/61533",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020325",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020325",
    "nando_id": "NANDO:2200021"
  },
  {
    "id": "C2347761",
    "id2": "MedGen UID:389541",
    "medgen_label": "Childhood myelodysplastic syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/389541",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0044873",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0044873",
    "nando_id": "NANDO:2200019"
  },
  {
    "id": "C0023480",
    "id2": "MedGen UID:44125",
    "medgen_label": "Chronic myelomonocytic leukemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44125",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020311",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020311",
    "nando_id": "NANDO:2200014"
  },
  {
    "id": "C0026850",
    "id2": "MedGen UID:44527",
    "medgen_label": "Muscular dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44527",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020121",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020121",
    "nando_id": "NANDO:2100233"
  },
  {
    "id": "C0270960",
    "id2": "MedGen UID:124381",
    "medgen_label": "Congenital myopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/124381",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019952",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019952",
    "nando_id": "NANDO:2100234"
  },
  {
    "id": "C0349636",
    "id2": "MedGen UID:83896",
    "medgen_label": "Precursor B-cell acute lymphoblastic leukemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/83896",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0020511",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020511",
    "nando_id": "NANDO:2200022"
  },
  {
    "id": "C0349636",
    "id2": "MedGen UID:83896",
    "medgen_label": "Precursor B-cell acute lymphoblastic leukemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/83896",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020511",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020511",
    "nando_id": "NANDO:2200001"
  },
  {
    "id": "C0392788",
    "id2": "MedGen UID:140278",
    "medgen_label": "Extranodal nasal NK/T cell lymphoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/140278",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019472",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019472",
    "nando_id": "NANDO:2200027"
  },
  {
    "id": "C0522624",
    "id2": "MedGen UID:99306",
    "medgen_label": "Subcutaneous panniculitis-like T-cell lymphoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/99306",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019475",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019475",
    "nando_id": "NANDO:2200030"
  },
  {
    "id": "C0342844",
    "id2": "MedGen UID:575248",
    "medgen_label": "Glycoprotein metabolism disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/575248",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0045010",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0045010",
    "nando_id": "NANDO:2100301"
  },
  {
    "id": "C0280141",
    "id2": "MedGen UID:79081",
    "medgen_label": "Acute undifferentiated leukemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/79081",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020321",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020321",
    "nando_id": "NANDO:2200017"
  },
  {
    "id": "C1879321",
    "id2": "MedGen UID:361829",
    "medgen_label": "Acute myeloblastic leukemia with maturation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/361829",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020320",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020320",
    "nando_id": "NANDO:2200006"
  },
  {
    "id": "C2826025",
    "id2": "MedGen UID:417342",
    "medgen_label": "Mixed phenotype acute leukemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/417342",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020743",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020743",
    "nando_id": "NANDO:2200018"
  },
  {
    "id": "C0751778",
    "id2": "MedGen UID:199732",
    "medgen_label": "Progressive myoclonic epilepsy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/199732",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020074",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020074",
    "nando_id": "NANDO:2100237"
  },
  {
    "id": "C1292758",
    "id2": "MedGen UID:266232",
    "medgen_label": "T-lymphoblastic lymphoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/266232",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0044917",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0044917",
    "nando_id": "NANDO:2200023"
  },
  {
    "id": "C0006264",
    "id2": "MedGen UID:2735",
    "medgen_label": "Bronchial neoplasm",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/2735",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002807",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002807",
    "nando_id": "NANDO:2200081"
  },
  {
    "id": "C0007115",
    "id2": "MedGen UID:2869",
    "medgen_label": "Malignant tumor of thyroid gland",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/2869",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002108",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002108",
    "nando_id": "NANDO:2200074"
  },
  {
    "id": "C0206651",
    "id2": "MedGen UID:104909",
    "medgen_label": "Clear cell sarcoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/104909",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002926",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002926",
    "nando_id": "NANDO:2200062"
  },
  {
    "id": "C0206743",
    "id2": "MedGen UID:64646",
    "medgen_label": "Rhabdoid tumor",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/64646",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002728",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002728",
    "nando_id": "NANDO:2200057"
  },
  {
    "id": "C0221238",
    "id2": "MedGen UID:66364",
    "medgen_label": "Mesangial proliferative glomerulonephritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/66364",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0003139",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003139",
    "nando_id": "NANDO:2200122"
  },
  {
    "id": "C0027809",
    "id2": "MedGen UID:45053",
    "medgen_label": "Schwannoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/45053",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002546",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002546",
    "nando_id": "NANDO:2200103"
  },
  {
    "id": "C0948750",
    "id2": "MedGen UID:215302",
    "medgen_label": "Salivary gland carcinoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/215302",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000521",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000521",
    "nando_id": "NANDO:2200076"
  },
  {
    "id": "C1368910",
    "id2": "MedGen UID:277967",
    "medgen_label": "Mature teratoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/277967",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0003517",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003517",
    "nando_id": "NANDO:2200105"
  },
  {
    "id": "C3887678",
    "id2": "MedGen UID:854517",
    "medgen_label": "Central primitive neuroectodermal tumor",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/854517",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000640",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000640",
    "nando_id": "NANDO:2200099"
  },
  {
    "id": "C0278510",
    "id2": "MedGen UID:75829",
    "medgen_label": "Childhood medulloblastoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75829",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0002797",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002797",
    "nando_id": "NANDO:2200090"
  },
  {
    "id": "C0278595",
    "id2": "MedGen UID:75840",
    "medgen_label": "Adult fibrosarcoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75840",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0002676",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002676",
    "nando_id": "NANDO:2200060"
  },
  {
    "id": "C0278608",
    "id2": "MedGen UID:75842",
    "medgen_label": "Adult liposarcoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75842",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0003585",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003585",
    "nando_id": "NANDO:2200065"
  },
  {
    "id": "C0278876",
    "id2": "MedGen UID:78898",
    "medgen_label": "Adult medulloblastoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78898",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0002794",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002794",
    "nando_id": "NANDO:2200090"
  },
  {
    "id": "C0279070",
    "id2": "MedGen UID:75924",
    "medgen_label": "Adult oligodendroglioma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75924",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0002543",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002543",
    "nando_id": "NANDO:2200089"
  },
  {
    "id": "C0279981",
    "id2": "MedGen UID:124685",
    "medgen_label": "Pediatric fibrosarcoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/124685",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0002678",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002678",
    "nando_id": "NANDO:2200060"
  },
  {
    "id": "C0280475",
    "id2": "MedGen UID:76116",
    "medgen_label": "Childhood oligodendroglioma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/76116",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0002540",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002540",
    "nando_id": "NANDO:2200089"
  },
  {
    "id": "C0280656",
    "id2": "MedGen UID:79156",
    "medgen_label": "Pediatric meningioma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/79156",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0003057",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003057",
    "nando_id": "NANDO:2200094"
  },
  {
    "id": "C0013377",
    "id2": "MedGen UID:41680",
    "medgen_label": "Dysgerminoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/41680",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0003002",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003002",
    "nando_id": "NANDO:2200066"
  },
  {
    "id": "C0017662",
    "id2": "MedGen UID:9033",
    "medgen_label": "Mesangiocapillary glomerulonephritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9033",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002461",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002461",
    "nando_id": "NANDO:2200123"
  },
  {
    "id": "C1332895",
    "id2": "MedGen UID:234105",
    "medgen_label": "Central nervous system teratoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/234105",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002718",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002718",
    "nando_id": "NANDO:2200104"
  },
  {
    "id": "C1332986",
    "id2": "MedGen UID:272464",
    "medgen_label": "Pediatric osteosarcoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/272464",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0002623",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002623",
    "nando_id": "NANDO:2200048"
  },
  {
    "id": "C0007134",
    "id2": "MedGen UID:766",
    "medgen_label": "Renal cell carcinoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/766",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005086",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005086",
    "nando_id": "NANDO:2200045"
  },
  {
    "id": "C0008441",
    "id2": "MedGen UID:40270",
    "medgen_label": "Chondroblastoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/40270",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0004997",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004997",
    "nando_id": "NANDO:2200051"
  },
  {
    "id": "C0008479",
    "id2": "MedGen UID:3054",
    "medgen_label": "Chondrosarcoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/3054",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008977",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008977",
    "nando_id": "NANDO:2200050"
  },
  {
    "id": "C0008487",
    "id2": "MedGen UID:40277",
    "medgen_label": "Chordoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/40277",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008978",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008978",
    "nando_id": "NANDO:2200098"
  },
  {
    "id": "C0008497",
    "id2": "MedGen UID:40278",
    "medgen_label": "Choriocarcinoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/40278",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005207",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005207",
    "nando_id": "NANDO:2200070"
  },
  {
    "id": "C0010276",
    "id2": "MedGen UID:41339",
    "medgen_label": "Craniopharyngioma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/41339",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018907",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018907",
    "nando_id": "NANDO:2200091"
  },
  {
    "id": "C0205770",
    "id2": "MedGen UID:64439",
    "medgen_label": "Choroid plexus papilloma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/64439",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009837",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009837",
    "nando_id": "NANDO:2200093"
  },
  {
    "id": "C0205969",
    "id2": "MedGen UID:60049",
    "medgen_label": "Thymic carcinoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/60049",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006451",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006451",
    "nando_id": "NANDO:2200079"
  },
  {
    "id": "C0206624",
    "id2": "MedGen UID:61644",
    "medgen_label": "Hepatoblastoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/61644",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018666",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018666",
    "nando_id": "NANDO:2200046"
  },
  {
    "id": "C0206657",
    "id2": "MedGen UID:61652",
    "medgen_label": "Alveolar soft part sarcoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/61652",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011655",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011655",
    "nando_id": "NANDO:2200063"
  },
  {
    "id": "C0206659",
    "id2": "MedGen UID:61653",
    "medgen_label": "Embryonal carcinoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/61653",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005440",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005440",
    "nando_id": "NANDO:2200067"
  },
  {
    "id": "C0206686",
    "id2": "MedGen UID:104917",
    "medgen_label": "Adrenal cortex carcinoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/104917",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006639",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006639",
    "nando_id": "NANDO:2200073"
  },
  {
    "id": "C0206716",
    "id2": "MedGen UID:60216",
    "medgen_label": "Ganglioglioma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/60216",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016733",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016733",
    "nando_id": "NANDO:2200096"
  },
  {
    "id": "C0206718",
    "id2": "MedGen UID:60218",
    "medgen_label": "Ganglioneuroblastoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/60218",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005035",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005035",
    "nando_id": "NANDO:2200041"
  },
  {
    "id": "C0206724",
    "id2": "MedGen UID:104926",
    "medgen_label": "Sex cord-stromal tumor",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/104926",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006055",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006055",
    "nando_id": "NANDO:2200072"
  },
  {
    "id": "C2239176",
    "id2": "MedGen UID:389187",
    "medgen_label": "Hepatocellular carcinoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/389187",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007256",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007256",
    "nando_id": "NANDO:2200047"
  },
  {
    "id": "C5779630",
    "id2": "MedGen UID:1830324",
    "medgen_label": "Gangliocytoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1830324",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016730",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016730",
    "nando_id": "NANDO:2200097"
  },
  {
    "id": "C0023269",
    "id2": "MedGen UID:9711",
    "medgen_label": "Leiomyosarcoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9711",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005058",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005058",
    "nando_id": "NANDO:2200064"
  },
  {
    "id": "C0023827",
    "id2": "MedGen UID:44177",
    "medgen_label": "Liposarcoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44177",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005060",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005060",
    "nando_id": "NANDO:2200065"
  },
  {
    "id": "C0025149",
    "id2": "MedGen UID:7517",
    "medgen_label": "Medulloblastoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7517",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007959",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007959",
    "nando_id": "NANDO:2200090"
  },
  {
    "id": "C0025202",
    "id2": "MedGen UID:9944",
    "medgen_label": "Melanoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9944",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005105",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005105",
    "nando_id": "NANDO:2200077"
  },
  {
    "id": "C0025286",
    "id2": "MedGen UID:7532",
    "medgen_label": "Meningioma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7532",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016642",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016642",
    "nando_id": "NANDO:2200094"
  },
  {
    "id": "C0027721",
    "id2": "MedGen UID:10307",
    "medgen_label": "Lipoid nephrosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10307",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006835",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006835",
    "nando_id": "NANDO:2200112"
  },
  {
    "id": "C0027819",
    "id2": "MedGen UID:18012",
    "medgen_label": "Neuroblastoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/18012",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005072",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005072",
    "nando_id": "NANDO:2200040"
  },
  {
    "id": "C0028945",
    "id2": "MedGen UID:45190",
    "medgen_label": "Oligodendroglioma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/45190",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016695",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016695",
    "nando_id": "NANDO:2200089"
  },
  {
    "id": "C0029463",
    "id2": "MedGen UID:10501",
    "medgen_label": "Osteosarcoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10501",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009807",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009807",
    "nando_id": "NANDO:2200048"
  },
  {
    "id": "C0403399",
    "id2": "MedGen UID:98011",
    "medgen_label": "Finnish congenital nephrotic syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/98011",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009732",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009732",
    "nando_id": "NANDO:2200110"
  },
  {
    "id": "C0549473",
    "id2": "MedGen UID:107811",
    "medgen_label": "Thyroid gland carcinoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/107811",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0015075",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015075",
    "nando_id": "NANDO:2200074"
  },
  {
    "id": "C0553580",
    "id2": "MedGen UID:107816",
    "medgen_label": "Ewing sarcoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/107816",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012817",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012817",
    "nando_id": "NANDO:2200053"
  },
  {
    "id": "C0917890",
    "id2": "MedGen UID:183004",
    "medgen_label": "Pineocytoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/183004",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016723",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016723",
    "nando_id": "NANDO:2200092"
  },
  {
    "id": "C0950121",
    "id2": "MedGen UID:181980",
    "medgen_label": "Drash syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/181980",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008682",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008682",
    "nando_id": "NANDO:2200116"
  },
  {
    "id": "C1260327",
    "id2": "MedGen UID:266041",
    "medgen_label": "Langerhans cell sarcoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/266041",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019480",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019480",
    "nando_id": "NANDO:2200036"
  },
  {
    "id": "C1266144",
    "id2": "MedGen UID:266105",
    "medgen_label": "Pleuropulmonary blastoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/266105",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011014",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011014",
    "nando_id": "NANDO:2200080"
  },
  {
    "id": "C1266184",
    "id2": "MedGen UID:226853",
    "medgen_label": "Atypical teratoid rhabdoid tumor",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/226853",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020560",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020560",
    "nando_id": "NANDO:2200101"
  },
  {
    "id": "C0334488",
    "id2": "MedGen UID:90791",
    "medgen_label": "Clear cell sarcoma of kidney",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/90791",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005006",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005006",
    "nando_id": "NANDO:2200044"
  },
  {
    "id": "C0334489",
    "id2": "MedGen UID:87250",
    "medgen_label": "Pancreatoblastoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/87250",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019035",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019035",
    "nando_id": "NANDO:2200082"
  },
  {
    "id": "C0334518",
    "id2": "MedGen UID:83160",
    "medgen_label": "Polyembryoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/83160",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015863",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015863",
    "nando_id": "NANDO:2200068"
  },
  {
    "id": "C0334520",
    "id2": "MedGen UID:90798",
    "medgen_label": "Immature teratoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/90798",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0024746",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0024746",
    "nando_id": "NANDO:2200106"
  },
  {
    "id": "C0334523",
    "id2": "MedGen UID:87256",
    "medgen_label": "Teratoma with malignant transformation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/87256",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006444",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006444",
    "nando_id": "NANDO:2200107"
  },
  {
    "id": "C0334524",
    "id2": "MedGen UID:87257",
    "medgen_label": "Mixed germ cell tumor",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/87257",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015864",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015864",
    "nando_id": "NANDO:2200071"
  },
  {
    "id": "C0334552",
    "id2": "MedGen UID:87263",
    "medgen_label": "Malignancy in giant cell tumor of bone",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/87263",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006287",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006287",
    "nando_id": "NANDO:2200052"
  },
  {
    "id": "C0334579",
    "id2": "MedGen UID:137784",
    "medgen_label": "Astrocytoma, anaplastic",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/137784",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016684",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016684",
    "nando_id": "NANDO:2200086"
  },
  {
    "id": "C0334583",
    "id2": "MedGen UID:87271",
    "medgen_label": "Pilocytic astrocytoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/87271",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016691",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016691",
    "nando_id": "NANDO:2200084"
  },
  {
    "id": "C0684337",
    "id2": "MedGen UID:151926",
    "medgen_label": "Peripheral primitive neuroectodermal tumor",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/151926",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018271",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018271",
    "nando_id": "NANDO:2200054"
  },
  {
    "id": "C0684337",
    "id2": "MedGen UID:151926",
    "medgen_label": "Peripheral primitive neuroectodermal tumor",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/151926",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018271",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018271",
    "nando_id": "NANDO:2200055"
  },
  {
    "id": "C1377598",
    "id2": "MedGen UID:277987",
    "medgen_label": "Childhood germ cell brain tumor",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/277987",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0004218",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004218",
    "nando_id": "NANDO:2200108"
  },
  {
    "id": "C1836876",
    "id2": "MedGen UID:373199",
    "medgen_label": "Pierson syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/373199",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012184",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012184",
    "nando_id": "NANDO:2200117"
  },
  {
    "id": "C1839543",
    "id2": "MedGen UID:374250",
    "medgen_label": "Central nervous system malformation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/374250",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020022",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020022",
    "nando_id": "NANDO:2200118"
  },
  {
    "id": "C4551683",
    "id2": "MedGen UID:1636437",
    "medgen_label": "Adrenal pheochromocytoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1636437",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0004974",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004974",
    "nando_id": "NANDO:2200078"
  },
  {
    "id": "C0032000",
    "id2": "MedGen UID:45933",
    "medgen_label": "Pituitary adenoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/45933",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006373",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006373",
    "nando_id": "NANDO:2200095"
  },
  {
    "id": "C0035335",
    "id2": "MedGen UID:20552",
    "medgen_label": "Retinoblastoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/20552",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008380",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008380",
    "nando_id": "NANDO:2200042"
  },
  {
    "id": "C0035412",
    "id2": "MedGen UID:20561",
    "medgen_label": "Rhabdomyosarcoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/20561",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005212",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005212",
    "nando_id": "NANDO:2200056"
  },
  {
    "id": "C0039101",
    "id2": "MedGen UID:21050",
    "medgen_label": "Synovial sarcoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21050",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010434",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010434",
    "nando_id": "NANDO:2200061"
  },
  {
    "id": "C0043324",
    "id2": "MedGen UID:12179",
    "medgen_label": "Juvenile xanthogranuloma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/12179",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015534",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015534",
    "nando_id": "NANDO:2200037"
  },
  {
    "id": "C0278878",
    "id2": "MedGen UID:124527",
    "medgen_label": "Adult glioblastoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/124527",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0020690",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020690",
    "nando_id": "NANDO:2200087"
  },
  {
    "id": "C0279984",
    "id2": "MedGen UID:83580",
    "medgen_label": "Pediatric liposarcoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/83580",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0003587",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003587",
    "nando_id": "NANDO:2200065"
  },
  {
    "id": "C0280785",
    "id2": "MedGen UID:83708",
    "medgen_label": "Diffuse astrocytoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/83708",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016686",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016686",
    "nando_id": "NANDO:2200085"
  },
  {
    "id": "C0281508",
    "id2": "MedGen UID:83833",
    "medgen_label": "Desmoplastic small round cell tumor",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/83833",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019373",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019373",
    "nando_id": "NANDO:2200059"
  },
  {
    "id": "C0014084",
    "id2": "MedGen UID:41775",
    "medgen_label": "Enchondromatosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/41775",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0008145",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008145",
    "nando_id": "NANDO:2200049"
  },
  {
    "id": "C0014145",
    "id2": "MedGen UID:41782",
    "medgen_label": "Yolk sac tumor",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/41782",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005744",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005744",
    "nando_id": "NANDO:2200069"
  },
  {
    "id": "C0014474",
    "id2": "MedGen UID:41825",
    "medgen_label": "Ependymoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/41825",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016698",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016698",
    "nando_id": "NANDO:2200088"
  },
  {
    "id": "C0015306",
    "id2": "MedGen UID:4612",
    "medgen_label": "Multiple congenital exostosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/4612",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0005508",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005508",
    "nando_id": "NANDO:2200049"
  },
  {
    "id": "C0016057",
    "id2": "MedGen UID:5178",
    "medgen_label": "Fibrosarcoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5178",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005164",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005164",
    "nando_id": "NANDO:2200060"
  },
  {
    "id": "C0017636",
    "id2": "MedGen UID:42228",
    "medgen_label": "Glioblastoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/42228",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018177",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018177",
    "nando_id": "NANDO:2200087"
  },
  {
    "id": "C0017661",
    "id2": "MedGen UID:9032",
    "medgen_label": "IgA glomerulonephritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9032",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005342",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005342",
    "nando_id": "NANDO:2200121"
  },
  {
    "id": "C0017665",
    "id2": "MedGen UID:42231",
    "medgen_label": "Membranous nephropathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/42231",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005376",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005376",
    "nando_id": "NANDO:2200114"
  },
  {
    "id": "C0019625",
    "id2": "MedGen UID:9266",
    "medgen_label": "Sinus histiocytosis with massive lymphadenopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9266",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006412",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006412",
    "nando_id": "NANDO:2200039"
  },
  {
    "id": "C0751690",
    "id2": "MedGen UID:155614",
    "medgen_label": "Malignant peripheral nerve sheath tumor",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155614",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017827",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017827",
    "nando_id": "NANDO:2200102"
  },
  {
    "id": "C0855073",
    "id2": "MedGen UID:163512",
    "medgen_label": "Undifferentiated (embryonal) sarcoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/163512",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005102",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005102",
    "nando_id": "NANDO:2200058"
  },
  {
    "id": "C0878675",
    "id2": "MedGen UID:163902",
    "medgen_label": "Erdheim-Chester disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/163902",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018153",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018153",
    "nando_id": "NANDO:2200038"
  },
  {
    "id": "C1332993",
    "id2": "MedGen UID:234136",
    "medgen_label": "Childhood ovarian yolk sac tumor",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/234136",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0003759",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003759",
    "nando_id": "NANDO:2200069"
  },
  {
    "id": "C1332995",
    "id2": "MedGen UID:232355",
    "medgen_label": "Childhood pilocytic astrocytoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/232355",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0004000",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004000",
    "nando_id": "NANDO:2200084"
  },
  {
    "id": "CN304703",
    "id2": "MedGen UID:988496",
    "medgen_label": "Primary membranoproliferative glomerulonephritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/988496",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018904",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018904",
    "nando_id": "NANDO:2200123"
  },
  {
    "id": "CN305775",
    "id2": "MedGen UID:989515",
    "medgen_label": "Kidney Wilms tumor",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/989515",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019004",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019004",
    "nando_id": "NANDO:2200043"
  },
  {
    "id": "CN327126",
    "id2": "MedGen UID:1008296",
    "medgen_label": "Inherited focal segmental glomerulosclerosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1008296",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005363",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005363",
    "nando_id": "NANDO:2200113"
  },
  {
    "id": "CN375949",
    "id2": "MedGen UID:1052115",
    "medgen_label": "Renal cell adenocarcinoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1052115",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0005549",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005549",
    "nando_id": "NANDO:2200045"
  },
  {
    "id": "C1567741",
    "id2": "MedGen UID:339209",
    "medgen_label": "Alport syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/339209",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018965",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018965",
    "nando_id": "NANDO:2200126"
  },
  {
    "id": "C0001126",
    "id2": "MedGen UID:90",
    "medgen_label": "Renal tubular acidosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/90",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001909",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001909",
    "nando_id": "NANDO:2200144"
  },
  {
    "id": "C0002726",
    "id2": "MedGen UID:272",
    "medgen_label": "Amyloidosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/272",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0019065",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019065",
    "nando_id": "NANDO:2200138"
  },
  {
    "id": "C0004775",
    "id2": "MedGen UID:2172",
    "medgen_label": "Bartter syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/2172",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015231",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015231",
    "nando_id": "NANDO:2200146"
  },
  {
    "id": "C0008780",
    "id2": "MedGen UID:3467",
    "medgen_label": "Primary ciliary dyskinesia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/3467",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0016575",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016575",
    "nando_id": "NANDO:2200204"
  },
  {
    "id": "C2673196",
    "id2": "MedGen UID:382034",
    "medgen_label": "Lipoprotein glomerulopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/382034",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012725",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012725",
    "nando_id": "NANDO:2200134"
  },
  {
    "id": "C2931788",
    "id2": "MedGen UID:444141",
    "medgen_label": "Atypical hemolytic-uremic syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/444141",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016244",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016244",
    "nando_id": "NANDO:2200131"
  },
  {
    "id": "C0022680",
    "id2": "MedGen UID:9639",
    "medgen_label": "Polycystic kidney disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9639",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020642",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020642",
    "nando_id": "NANDO:2200152"
  },
  {
    "id": "C0024143",
    "id2": "MedGen UID:6147",
    "medgen_label": "Lupus nephritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6147",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005556",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005556",
    "nando_id": "NANDO:2200128"
  },
  {
    "id": "C0027341",
    "id2": "MedGen UID:10257",
    "medgen_label": "Nail-patella syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10257",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008061",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008061",
    "nando_id": "NANDO:2200132"
  },
  {
    "id": "C0266295",
    "id2": "MedGen UID:120571",
    "medgen_label": "Renal hypoplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120571",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019637",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019637",
    "nando_id": "NANDO:2200155"
  },
  {
    "id": "C0268113",
    "id2": "MedGen UID:75651",
    "medgen_label": "Familial juvenile gout",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75651",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000608",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000608",
    "nando_id": "NANDO:2200139"
  },
  {
    "id": "C0268389",
    "id2": "MedGen UID:82799",
    "medgen_label": "Familial visceral amyloidosis, Ostertag type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82799",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0007099",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007099",
    "nando_id": "NANDO:2200138"
  },
  {
    "id": "C0268450",
    "id2": "MedGen UID:75681",
    "medgen_label": "Familial hypokalemia-hypomagnesemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75681",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009904",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009904",
    "nando_id": "NANDO:2200145"
  },
  {
    "id": "C0396051",
    "id2": "MedGen UID:97973",
    "medgen_label": "Congenital subglottic stenosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/97973",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0015395",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015395",
    "nando_id": "NANDO:2200190"
  },
  {
    "id": "C0403529",
    "id2": "MedGen UID:140788",
    "medgen_label": "Anti-glomerular basement membrane disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/140788",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009303",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009303",
    "nando_id": "NANDO:2200125"
  },
  {
    "id": "C1855681",
    "id2": "MedGen UID:343406",
    "medgen_label": "Nephronophthisis 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/343406",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009728",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009728",
    "nando_id": "NANDO:2200140"
  },
  {
    "id": "C0085413",
    "id2": "MedGen UID:88404",
    "medgen_label": "Autosomal dominant polycystic kidney disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/88404",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0004691",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004691",
    "nando_id": "NANDO:2200153"
  },
  {
    "id": "C0085548",
    "id2": "MedGen UID:39076",
    "medgen_label": "Autosomal recessive polycystic kidney disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/39076",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009889",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009889",
    "nando_id": "NANDO:2200154"
  },
  {
    "id": "C0085697",
    "id2": "MedGen UID:39090",
    "medgen_label": "Chronic pyelonephritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/39090",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001110",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001110",
    "nando_id": "NANDO:2200137"
  },
  {
    "id": "C0687120",
    "id2": "MedGen UID:146912",
    "medgen_label": "Nephronophthisis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/146912",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019005",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019005",
    "nando_id": "NANDO:2200140"
  },
  {
    "id": "C0687120",
    "id2": "MedGen UID:146912",
    "medgen_label": "Nephronophthisis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/146912",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0019005",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019005",
    "nando_id": "NANDO:2200170"
  },
  {
    "id": "C3888104",
    "id2": "MedGen UID:854773",
    "medgen_label": "Fibronectin glomerulopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/854773",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007671",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007671",
    "nando_id": "NANDO:2200133"
  },
  {
    "id": "C0041349",
    "id2": "MedGen UID:11952",
    "medgen_label": "Interstitial nephritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/11952",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001085",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001085",
    "nando_id": "NANDO:2200136"
  },
  {
    "id": "C0020544",
    "id2": "MedGen UID:5700",
    "medgen_label": "Renal hypertension",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5700",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0001105",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001105",
    "nando_id": "NANDO:2200141"
  },
  {
    "id": "C0020545",
    "id2": "MedGen UID:43786",
    "medgen_label": "Renovascular hypertension",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/43786",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006947",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006947",
    "nando_id": "NANDO:2200141"
  },
  {
    "id": "C0265756",
    "id2": "MedGen UID:78572",
    "medgen_label": "Laryngeal atresia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78572",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0007879",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007879",
    "nando_id": "NANDO:2200190"
  },
  {
    "id": "C0006267",
    "id2": "MedGen UID:14234",
    "medgen_label": "Bronchiectasis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/14234",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0004822",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004822",
    "nando_id": "NANDO:2200206"
  },
  {
    "id": "C0006272",
    "id2": "MedGen UID:665",
    "medgen_label": "Bronchiolitis obliterans with obstructive pulmonary disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/665",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015265",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015265",
    "nando_id": "NANDO:2200209"
  },
  {
    "id": "C0008780",
    "id2": "MedGen UID:3467",
    "medgen_label": "Primary ciliary dyskinesia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/3467",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016575",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016575",
    "nando_id": "NANDO:2200203"
  },
  {
    "id": "C0010674",
    "id2": "MedGen UID:41393",
    "medgen_label": "Cystic fibrosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/41393",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009061",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009061",
    "nando_id": "NANDO:2200205"
  },
  {
    "id": "C0155700",
    "id2": "MedGen UID:102340",
    "medgen_label": "Mobitz II atrioventricular block",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/102340",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001261",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001261",
    "nando_id": "NANDO:2200213"
  },
  {
    "id": "C0155912",
    "id2": "MedGen UID:56374",
    "medgen_label": "PULMONARY ALVEOLAR MICROLITHIASIS",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/56374",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009928",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009928",
    "nando_id": "NANDO:2200202"
  },
  {
    "id": "C0178426",
    "id2": "MedGen UID:472617",
    "medgen_label": "Potter sequence",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/472617",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001558",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001558",
    "nando_id": "NANDO:2200157"
  },
  {
    "id": "C0178879",
    "id2": "MedGen UID:64247",
    "medgen_label": "Urinary tract obstruction",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/64247",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0003330",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003330",
    "nando_id": "NANDO:2200178"
  },
  {
    "id": "C2350236",
    "id2": "MedGen UID:389939",
    "medgen_label": "Idiopathic interstitial pneumonia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/389939",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002429",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002429",
    "nando_id": "NANDO:2200199"
  },
  {
    "id": "C0022681",
    "id2": "MedGen UID:5970",
    "medgen_label": "Medullary sponge kidney",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5970",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015268",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015268",
    "nando_id": "NANDO:2200173"
  },
  {
    "id": "C0028860",
    "id2": "MedGen UID:18145",
    "medgen_label": "Lowe syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/18145",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010645",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010645",
    "nando_id": "NANDO:2200188"
  },
  {
    "id": "C0266316",
    "id2": "MedGen UID:78594",
    "medgen_label": "Congenital hydronephrosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78594",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007741",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007741",
    "nando_id": "NANDO:2200176"
  },
  {
    "id": "C0431694",
    "id2": "MedGen UID:609100",
    "medgen_label": "Oligomeganephronia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/609100",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016407",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016407",
    "nando_id": "NANDO:2200159"
  },
  {
    "id": "C0431719",
    "id2": "MedGen UID:609113",
    "medgen_label": "Multiloculated renal cyst",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/609113",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019983",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019983",
    "nando_id": "NANDO:2200171"
  },
  {
    "id": "C0542519",
    "id2": "MedGen UID:154237",
    "medgen_label": "Renal agenesis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/154237",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018470",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018470",
    "nando_id": "NANDO:2200156"
  },
  {
    "id": "C0948187",
    "id2": "MedGen UID:215296",
    "medgen_label": "Tracheomalacia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/215296",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019804",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019804",
    "nando_id": "NANDO:2200195"
  },
  {
    "id": "C3536714",
    "id2": "MedGen UID:760690",
    "medgen_label": "Renal dysplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/760690",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019638",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019638",
    "nando_id": "NANDO:2200161"
  },
  {
    "id": "C3711368",
    "id2": "MedGen UID:777976",
    "medgen_label": "Hereditary pulmonary alveolar proteinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/777976",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012580",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012580",
    "nando_id": "NANDO:2200200"
  },
  {
    "id": "C3714581",
    "id2": "MedGen UID:811388",
    "medgen_label": "Multicystic kidney dysplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/811388",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015988",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015988",
    "nando_id": "NANDO:2200158"
  },
  {
    "id": "C4273898",
    "id2": "MedGen UID:903364",
    "medgen_label": "Congenital primary megaureter",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/903364",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018960",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018960",
    "nando_id": "NANDO:2200184"
  },
  {
    "id": "C3887499",
    "id2": "MedGen UID:854361",
    "medgen_label": "Renal cyst",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/854361",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002473",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002473",
    "nando_id": "NANDO:2200172"
  },
  {
    "id": "C0033770",
    "id2": "MedGen UID:18718",
    "medgen_label": "Prune belly syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/18718",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007032",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007032",
    "nando_id": "NANDO:2200185"
  },
  {
    "id": "C0037052",
    "id2": "MedGen UID:20749",
    "medgen_label": "Sick sinus syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/20749",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001823",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001823",
    "nando_id": "NANDO:2200212"
  },
  {
    "id": "C0040583",
    "id2": "MedGen UID:21227",
    "medgen_label": "Tracheal stenosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21227",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002568",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002568",
    "nando_id": "NANDO:2200194"
  },
  {
    "id": "C0041960",
    "id2": "MedGen UID:21778",
    "medgen_label": "Ureterocele",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21778",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008628",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008628",
    "nando_id": "NANDO:2200183"
  },
  {
    "id": "C0042580",
    "id2": "MedGen UID:21852",
    "medgen_label": "Vesicoureteral reflux",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21852",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006007",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006007",
    "nando_id": "NANDO:2200179"
  },
  {
    "id": "C1869116",
    "id2": "MedGen UID:358271",
    "medgen_label": "Inherited susceptibility to asthma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/358271",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010940",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010940",
    "nando_id": "NANDO:2200197"
  },
  {
    "id": "C5545379",
    "id2": "MedGen UID:1782490",
    "medgen_label": "Congenital megacalycosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1782490",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019639",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019639",
    "nando_id": "NANDO:2200177"
  },
  {
    "id": "C0015624",
    "id2": "MedGen UID:4653",
    "medgen_label": "Fanconi syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/4653",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001083",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001083",
    "nando_id": "NANDO:2200187"
  },
  {
    "id": "C0020807",
    "id2": "MedGen UID:9403",
    "medgen_label": "Idiopathic pulmonary hemosiderosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9403",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008346",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008346",
    "nando_id": "NANDO:2200207"
  },
  {
    "id": "C0235833",
    "id2": "MedGen UID:68625",
    "medgen_label": "Congenital diaphragmatic hernia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/68625",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005711",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005711",
    "nando_id": "NANDO:2200210"
  },
  {
    "id": "C1735886",
    "id2": "MedGen UID:760471",
    "medgen_label": "Anomalous origin of left coronary artery from the pulmonary artery",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/760471",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000811",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000811",
    "nando_id": "NANDO:2200242"
  },
  {
    "id": "C0003486",
    "id2": "MedGen UID:362",
    "medgen_label": "Aortic aneurysm",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/362",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005160",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005160",
    "nando_id": "NANDO:2200294"
  },
  {
    "id": "C0003492",
    "id2": "MedGen UID:1617",
    "medgen_label": "Coarctation of aorta",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1617",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0007345",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007345",
    "nando_id": "NANDO:2200284"
  },
  {
    "id": "C0003492",
    "id2": "MedGen UID:1617",
    "medgen_label": "Coarctation of aorta",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1617",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007345",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007345",
    "nando_id": "NANDO:2200283"
  },
  {
    "id": "C0003499",
    "id2": "MedGen UID:2001",
    "medgen_label": "Supravalvar aortic stenosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/2001",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008504",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008504",
    "nando_id": "NANDO:2200285"
  },
  {
    "id": "C0004238",
    "id2": "MedGen UID:445",
    "medgen_label": "Atrial fibrillation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/445",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0004981",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004981",
    "nando_id": "NANDO:2200226"
  },
  {
    "id": "C0004239",
    "id2": "MedGen UID:13955",
    "medgen_label": "Atrial flutter",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/13955",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0005310",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005310",
    "nando_id": "NANDO:2200218"
  },
  {
    "id": "C0004239",
    "id2": "MedGen UID:13955",
    "medgen_label": "Atrial flutter",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/13955",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005310",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005310",
    "nando_id": "NANDO:2200225"
  },
  {
    "id": "C0007193",
    "id2": "MedGen UID:2880",
    "medgen_label": "Primary dilated cardiomyopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/2880",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005021",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005021",
    "nando_id": "NANDO:2200232"
  },
  {
    "id": "C0007194",
    "id2": "MedGen UID:2881",
    "medgen_label": "Hypertrophic cardiomyopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/2881",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005045",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005045",
    "nando_id": "NANDO:2200229"
  },
  {
    "id": "C0007196",
    "id2": "MedGen UID:40111",
    "medgen_label": "Restrictive cardiomyopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/40111",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005201",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005201",
    "nando_id": "NANDO:2200233"
  },
  {
    "id": "C0175702",
    "id2": "MedGen UID:59799",
    "medgen_label": "Williams syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/59799",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008678",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008678",
    "nando_id": "NANDO:2200286"
  },
  {
    "id": "C0023976",
    "id2": "MedGen UID:44193",
    "medgen_label": "Long QT syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44193",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002442",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002442",
    "nando_id": "NANDO:2200228"
  },
  {
    "id": "C0027051",
    "id2": "MedGen UID:10150",
    "medgen_label": "Myocardial infarction",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10150",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005068",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005068",
    "nando_id": "NANDO:2200248"
  },
  {
    "id": "C0031048",
    "id2": "MedGen UID:18378",
    "medgen_label": "Constrictive pericarditis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/18378",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006711",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006711",
    "nando_id": "NANDO:2200239"
  },
  {
    "id": "C0546959",
    "id2": "MedGen UID:107485",
    "medgen_label": "atrial tachycardia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/107485",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0005479",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005479",
    "nando_id": "NANDO:2200218"
  },
  {
    "id": "C0151517",
    "id2": "MedGen UID:56230",
    "medgen_label": "Third degree atrioventricular block",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/56230",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000468",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000468",
    "nando_id": "NANDO:2200214"
  },
  {
    "id": "C0152101",
    "id2": "MedGen UID:57746",
    "medgen_label": "Hypoplastic left heart syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/57746",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0004933",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004933",
    "nando_id": "NANDO:2200249"
  },
  {
    "id": "C0340375",
    "id2": "MedGen UID:90950",
    "medgen_label": "Subvalvular aortic stenosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/90950",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006987",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006987",
    "nando_id": "NANDO:2200277"
  },
  {
    "id": "C0344976",
    "id2": "MedGen UID:87492",
    "medgen_label": "Pulmonary atresia with ventricular septal defect",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/87492",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008343",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008343",
    "nando_id": "NANDO:2200252"
  },
  {
    "id": "C4551903",
    "id2": "MedGen UID:1648157",
    "medgen_label": "Congenital total pulmonary venous return anomaly",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1648157",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007130",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007130",
    "nando_id": "NANDO:2200271"
  },
  {
    "id": "C0034084",
    "id2": "MedGen UID:11030",
    "medgen_label": "Pulmonary subvalvular stenosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/11030",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006935",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006935",
    "nando_id": "NANDO:2200276"
  },
  {
    "id": "C0039685",
    "id2": "MedGen UID:21498",
    "medgen_label": "Tetralogy of Fallot",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21498",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008542",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008542",
    "nando_id": "NANDO:2200254"
  },
  {
    "id": "C0040761",
    "id2": "MedGen UID:21245",
    "medgen_label": "Transposition of the great arteries",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21245",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000153",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000153",
    "nando_id": "NANDO:2200258"
  },
  {
    "id": "C0040961",
    "id2": "MedGen UID:11911",
    "medgen_label": "Tricuspid regurgitation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/11911",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002870",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002870",
    "nando_id": "NANDO:2200301"
  },
  {
    "id": "C0040963",
    "id2": "MedGen UID:21678",
    "medgen_label": "Tricuspid stenosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21678",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005997",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005997",
    "nando_id": "NANDO:2200300"
  },
  {
    "id": "C0042510",
    "id2": "MedGen UID:21844",
    "medgen_label": "Ventricular fibrillation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21844",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000190",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000190",
    "nando_id": "NANDO:2200227"
  },
  {
    "id": "C0043202",
    "id2": "MedGen UID:12162",
    "medgen_label": "Wolff-Parkinson-White pattern",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/12162",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008685",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008685",
    "nando_id": "NANDO:2200217"
  },
  {
    "id": "C0018789",
    "id2": "MedGen UID:42360",
    "medgen_label": "Heart aneurysm",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/42360",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006779",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006779",
    "nando_id": "NANDO:2200234"
  },
  {
    "id": "C0018818",
    "id2": "MedGen UID:42366",
    "medgen_label": "Ventricular septal defect",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/42366",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002070",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002070",
    "nando_id": "NANDO:2200270"
  },
  {
    "id": "C0238074",
    "id2": "MedGen UID:116042",
    "medgen_label": "Chronic pulmonary heart disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/116042",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001493",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001493",
    "nando_id": "NANDO:2200299"
  },
  {
    "id": "C0242231",
    "id2": "MedGen UID:66859",
    "medgen_label": "Coronary artery stenosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/66859",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006715",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006715",
    "nando_id": "NANDO:2200246"
  },
  {
    "id": "C0003516",
    "id2": "MedGen UID:365",
    "medgen_label": "Aortopulmonary window",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/365",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0021902",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0021902",
    "nando_id": "NANDO:2200262"
  },
  {
    "id": "C0009995",
    "id2": "MedGen UID:3238",
    "medgen_label": "Triatrial heart",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/3238",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015450",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015450",
    "nando_id": "NANDO:2200263"
  },
  {
    "id": "C0158634",
    "id2": "MedGen UID:450995",
    "medgen_label": "Partial anomalous pulmonary venous return",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/450995",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020453",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020453",
    "nando_id": "NANDO:2200272"
  },
  {
    "id": "C0221215",
    "id2": "MedGen UID:65132",
    "medgen_label": "Complete atrioventricular canal",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/65132",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015273",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015273",
    "nando_id": "NANDO:2200269"
  },
  {
    "id": "C2239253",
    "id2": "MedGen UID:853730",
    "medgen_label": "Aneurysm of sinus of Valsalva",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/853730",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015197",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015197",
    "nando_id": "NANDO:2200293"
  },
  {
    "id": "C2973725",
    "id2": "MedGen UID:425404",
    "medgen_label": "Pulmonary arterial hypertension",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/425404",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015924",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015924",
    "nando_id": "NANDO:2200298"
  },
  {
    "id": "C0265809",
    "id2": "MedGen UID:120558",
    "medgen_label": "Double outlet left ventricle",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120558",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018090",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018090",
    "nando_id": "NANDO:2200257"
  },
  {
    "id": "C0265898",
    "id2": "MedGen UID:488822",
    "medgen_label": "Coronary artery fistula",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/488822",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016081",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016081",
    "nando_id": "NANDO:2200296"
  },
  {
    "id": "C0265905",
    "id2": "MedGen UID:120560",
    "medgen_label": "Absent pulmonary artery",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120560",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020007",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020007",
    "nando_id": "NANDO:2200282"
  },
  {
    "id": "C0349788",
    "id2": "MedGen UID:87618",
    "medgen_label": "Arrhythmogenic right ventricular cardiomyopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/87618",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016587",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016587",
    "nando_id": "NANDO:2200230"
  },
  {
    "id": "C0546315",
    "id2": "MedGen UID:903640",
    "medgen_label": "Cardiac diverticulum",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/903640",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0015677",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015677",
    "nando_id": "NANDO:2200234"
  },
  {
    "id": "C1141890",
    "id2": "MedGen UID:685787",
    "medgen_label": "Congenital long QT syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/685787",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0019171",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019171",
    "nando_id": "NANDO:2200228"
  },
  {
    "id": "C1857586",
    "id2": "MedGen UID:341803",
    "medgen_label": "Conotruncal heart malformations",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/341803",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016581",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016581",
    "nando_id": "NANDO:2200275"
  },
  {
    "id": "C3280212",
    "id2": "MedGen UID:481842",
    "medgen_label": "Supravalvular pulmonary stenosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/481842",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017870",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017870",
    "nando_id": "NANDO:2200278"
  },
  {
    "id": "C3496579",
    "id2": "MedGen UID:758831",
    "medgen_label": "Atypical coarctation of aorta",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/758831",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0015446",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015446",
    "nando_id": "NANDO:2200284"
  },
  {
    "id": "C0149530",
    "id2": "MedGen UID:57432",
    "medgen_label": "Congenital heart block",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/57432",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009326",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009326",
    "nando_id": "NANDO:2200214"
  },
  {
    "id": "C0152419",
    "id2": "MedGen UID:57773",
    "medgen_label": "Aortic arch interruption",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/57773",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009010",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009010",
    "nando_id": "NANDO:2200288"
  },
  {
    "id": "C0344616",
    "id2": "MedGen UID:87489",
    "medgen_label": "Congenitally corrected transposition of the great arteries",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/87489",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016301",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016301",
    "nando_id": "NANDO:2200259"
  },
  {
    "id": "C0344622",
    "id2": "MedGen UID:488862",
    "medgen_label": "Double inlet left ventricle",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/488862",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015451",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015451",
    "nando_id": "NANDO:2200250"
  },
  {
    "id": "C0344724",
    "id2": "MedGen UID:91034",
    "medgen_label": "Atrial septal defect, ostium secundum type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/91034",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020434",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020434",
    "nando_id": "NANDO:2200266"
  },
  {
    "id": "C0344730",
    "id2": "MedGen UID:138011",
    "medgen_label": "Sinus venosus atrial septal defect",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/138011",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020436",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020436",
    "nando_id": "NANDO:2200267"
  },
  {
    "id": "C0344947",
    "id2": "MedGen UID:576645",
    "medgen_label": "Congenital Gerbode defect",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/576645",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020428",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020428",
    "nando_id": "NANDO:2200274"
  },
  {
    "id": "C0344975",
    "id2": "MedGen UID:87491",
    "medgen_label": "Pulmonary atresia with intact ventricular septum",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/87491",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009931",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009931",
    "nando_id": "NANDO:2200253"
  },
  {
    "id": "C0344983",
    "id2": "MedGen UID:576671",
    "medgen_label": "Pulmonary valve agenesis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/576671",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020064",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020064",
    "nando_id": "NANDO:2200280"
  },
  {
    "id": "C3838927",
    "id2": "MedGen UID:824773",
    "medgen_label": "Pulmonary artery coming from the aorta",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/824773",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020391",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020391",
    "nando_id": "NANDO:2200281"
  },
  {
    "id": "C5574922",
    "id2": "MedGen UID:1803763",
    "medgen_label": "Catecholaminergic polymorphic ventricular tachycardia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1803763",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017990",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017990",
    "nando_id": "NANDO:2200221"
  },
  {
    "id": "C5574922",
    "id2": "MedGen UID:1803763",
    "medgen_label": "Catecholaminergic polymorphic ventricular tachycardia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1803763",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0017990",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017990",
    "nando_id": "NANDO:2200216"
  },
  {
    "id": "C0041207",
    "id2": "MedGen UID:52867",
    "medgen_label": "Persistent truncus arteriosus",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/52867",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018072",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018072",
    "nando_id": "NANDO:2200261"
  },
  {
    "id": "C1960469",
    "id2": "MedGen UID:450531",
    "medgen_label": "Left ventricular noncompaction",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/450531",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018901",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018901",
    "nando_id": "NANDO:2200231"
  },
  {
    "id": "C0013069",
    "id2": "MedGen UID:41649",
    "medgen_label": "Double outlet right ventricle",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/41649",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018089",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018089",
    "nando_id": "NANDO:2200256"
  },
  {
    "id": "C0013274",
    "id2": "MedGen UID:4415",
    "medgen_label": "Patent ductus arteriosus",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/4415",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011827",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011827",
    "nando_id": "NANDO:2200264"
  },
  {
    "id": "C0013481",
    "id2": "MedGen UID:4435",
    "medgen_label": "Ebstein anomaly",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/4435",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009144",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009144",
    "nando_id": "NANDO:2200260"
  },
  {
    "id": "C0014117",
    "id2": "MedGen UID:4041",
    "medgen_label": "Endocardial fibroelastosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/4041",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009169",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009169",
    "nando_id": "NANDO:2200235"
  },
  {
    "id": "C0016522",
    "id2": "MedGen UID:8891",
    "medgen_label": "Patent foramen ovale",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/8891",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0020439",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020439",
    "nando_id": "NANDO:2200266"
  },
  {
    "id": "C0018809",
    "id2": "MedGen UID:9172",
    "medgen_label": "Neoplasm of the heart",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9172",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0021209",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0021209",
    "nando_id": "NANDO:2200236"
  },
  {
    "id": "C0243002",
    "id2": "MedGen UID:67034",
    "medgen_label": "Tricuspid atresia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/67034",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011514",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011514",
    "nando_id": "NANDO:2200251"
  },
  {
    "id": "C4023290",
    "id2": "MedGen UID:868879",
    "medgen_label": "Partial atrioventricular canal",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/868879",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015275",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015275",
    "nando_id": "NANDO:2200268"
  },
  {
    "id": "C5680865",
    "id2": "MedGen UID:1826176",
    "medgen_label": "Congenital pulmonary veins atresia or stenosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1826176",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017864",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017864",
    "nando_id": "NANDO:2200273"
  },
  {
    "id": "C1849157",
    "id2": "MedGen UID:338622",
    "medgen_label": "Growth delay due to insulin-like growth factor I resistance",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/338622",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010038",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010038",
    "nando_id": "NANDO:2200320"
  },
  {
    "id": "C0001206",
    "id2": "MedGen UID:1304",
    "medgen_label": "Acromegaly",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1304",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019933",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019933",
    "nando_id": "NANDO:2200315"
  },
  {
    "id": "C0001231",
    "id2": "MedGen UID:103",
    "medgen_label": "Ectopic ACTH secretion syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/103",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0043472",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0043472",
    "nando_id": "NANDO:2200351"
  },
  {
    "id": "C0001403",
    "id2": "MedGen UID:1324",
    "medgen_label": "Primary adrenocortical insufficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1324",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0015129",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015129",
    "nando_id": "NANDO:2200359"
  },
  {
    "id": "C0001403",
    "id2": "MedGen UID:1324",
    "medgen_label": "Primary adrenocortical insufficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1324",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015129",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015129",
    "nando_id": "NANDO:2200360"
  },
  {
    "id": "C0001627",
    "id2": "MedGen UID:7900",
    "medgen_label": "Congenital adrenal hyperplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7900",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018479",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018479",
    "nando_id": "NANDO:2200370"
  },
  {
    "id": "C0003504",
    "id2": "MedGen UID:8153",
    "medgen_label": "Aortic regurgitation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/8153",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005648",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005648",
    "nando_id": "NANDO:2200307"
  },
  {
    "id": "C0003507",
    "id2": "MedGen UID:1621",
    "medgen_label": "Aortic valve stenosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1621",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0042981",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0042981",
    "nando_id": "NANDO:2200306"
  },
  {
    "id": "C0010308",
    "id2": "MedGen UID:41344",
    "medgen_label": "Congenital hypothyroidism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/41344",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018612",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018612",
    "nando_id": "NANDO:2200333"
  },
  {
    "id": "C0158619",
    "id2": "MedGen UID:510600",
    "medgen_label": "Congenital mitral valve insufficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/510600",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001298",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001298",
    "nando_id": "NANDO:2200303"
  },
  {
    "id": "C0162283",
    "id2": "MedGen UID:57876",
    "medgen_label": "Nephrogenic diabetes insipidus",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/57876",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016383",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016383",
    "nando_id": "NANDO:2200326"
  },
  {
    "id": "C0162809",
    "id2": "MedGen UID:102469",
    "medgen_label": "Hypogonadism with anosmia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/102469",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018800",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018800",
    "nando_id": "NANDO:2200381"
  },
  {
    "id": "C0206667",
    "id2": "MedGen UID:61654",
    "medgen_label": "Adrenocortical adenoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/61654",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0003924",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003924",
    "nando_id": "NANDO:2200352"
  },
  {
    "id": "C0221043",
    "id2": "MedGen UID:67439",
    "medgen_label": "Liddle syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/67439",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008323",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008323",
    "nando_id": "NANDO:2200363"
  },
  {
    "id": "C0221406",
    "id2": "MedGen UID:66381",
    "medgen_label": "Pituitary dependent hypercortisolism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/66381",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009050",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009050",
    "nando_id": "NANDO:2200350"
  },
  {
    "id": "C2062388",
    "id2": "MedGen UID:923388",
    "medgen_label": "Cushing syndrome due to macronodular adrenal hyperplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/923388",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009049",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009049",
    "nando_id": "NANDO:2200353"
  },
  {
    "id": "C2936858",
    "id2": "MedGen UID:424833",
    "medgen_label": "Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/424833",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008728",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008728",
    "nando_id": "NANDO:2200374"
  },
  {
    "id": "C2940786",
    "id2": "MedGen UID:424854",
    "medgen_label": "Thyroid hormone resistance syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/424854",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001328",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001328",
    "nando_id": "NANDO:2200341"
  },
  {
    "id": "C0022735",
    "id2": "MedGen UID:44033",
    "medgen_label": "Klinefelter syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44033",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006823",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006823",
    "nando_id": "NANDO:2200386"
  },
  {
    "id": "C0026269",
    "id2": "MedGen UID:44466",
    "medgen_label": "Mitral stenosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44466",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005852",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005852",
    "nando_id": "NANDO:2200302"
  },
  {
    "id": "C0265851",
    "id2": "MedGen UID:539536",
    "medgen_label": "Congenital supravalvular mitral ring",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/539536",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020400",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020400",
    "nando_id": "NANDO:2200308"
  },
  {
    "id": "C0266283",
    "id2": "MedGen UID:78591",
    "medgen_label": "Ectopic thyroid",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78591",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019854",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019854",
    "nando_id": "NANDO:2200330"
  },
  {
    "id": "C0268285",
    "id2": "MedGen UID:82782",
    "medgen_label": "Deficiency of steroid 17-alpha-monooxygenase",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82782",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008730",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008730",
    "nando_id": "NANDO:2200373"
  },
  {
    "id": "C0268292",
    "id2": "MedGen UID:82783",
    "medgen_label": "Deficiency of steroid 11-beta-monooxygenase",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82783",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008729",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008729",
    "nando_id": "NANDO:2200372"
  },
  {
    "id": "C0268436",
    "id2": "MedGen UID:82805",
    "medgen_label": "Pseudohypoaldosteronism type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82805",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019161",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019161",
    "nando_id": "NANDO:2200368"
  },
  {
    "id": "C1860042",
    "id2": "MedGen UID:348008",
    "medgen_label": "Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/348008",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013310",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013310",
    "nando_id": "NANDO:2200375"
  },
  {
    "id": "C3489796",
    "id2": "MedGen UID:483749",
    "medgen_label": "Thyroid hormone resistance, generalized, autosomal recessive",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/483749",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0010131",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010131",
    "nando_id": "NANDO:2200341"
  },
  {
    "id": "C4302200",
    "id2": "MedGen UID:927869",
    "medgen_label": "Congenital central hypothyroidism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/927869",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0016410",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016410",
    "nando_id": "NANDO:2200340"
  },
  {
    "id": "C4302200",
    "id2": "MedGen UID:927869",
    "medgen_label": "Congenital central hypothyroidism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/927869",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016410",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016410",
    "nando_id": "NANDO:2200332"
  },
  {
    "id": "C4751433",
    "id2": "MedGen UID:1651973",
    "medgen_label": "Late-onset isolated ACTH deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1651973",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016042",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016042",
    "nando_id": "NANDO:2200355"
  },
  {
    "id": "C0085859",
    "id2": "MedGen UID:39125",
    "medgen_label": "Polyglandular autoimmune syndrome, type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/39125",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009411",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009411",
    "nando_id": "NANDO:2200346"
  },
  {
    "id": "C0085860",
    "id2": "MedGen UID:39126",
    "medgen_label": "Polyglandular autoimmune syndrome, type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/39126",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010012",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010012",
    "nando_id": "NANDO:2200347"
  },
  {
    "id": "C0342471",
    "id2": "MedGen UID:452446",
    "medgen_label": "3 beta-Hydroxysteroid dehydrogenase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/452446",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008727",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008727",
    "nando_id": "NANDO:2200371"
  },
  {
    "id": "C0342482",
    "id2": "MedGen UID:87442",
    "medgen_label": "Congenital adrenal hypoplasia, X-linked",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/87442",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0010264",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010264",
    "nando_id": "NANDO:2200357"
  },
  {
    "id": "C0342488",
    "id2": "MedGen UID:90983",
    "medgen_label": "Apparent mineralocorticoid excess",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/90983",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009025",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009025",
    "nando_id": "NANDO:2200362"
  },
  {
    "id": "C0342543",
    "id2": "MedGen UID:90985",
    "medgen_label": "Central precocious puberty",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/90985",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019165",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019165",
    "nando_id": "NANDO:2200377"
  },
  {
    "id": "C0677607",
    "id2": "MedGen UID:151769",
    "medgen_label": "Hashimoto thyroiditis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/151769",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007699",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007699",
    "nando_id": "NANDO:2200335"
  },
  {
    "id": "C0685837",
    "id2": "MedGen UID:146899",
    "medgen_label": "46 XX gonadal dysgenesis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/146899",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009299",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009299",
    "nando_id": "NANDO:2200384"
  },
  {
    "id": "C0687720",
    "id2": "MedGen UID:146919",
    "medgen_label": "Central diabetes insipidus",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/146919",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015790",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015790",
    "nando_id": "NANDO:2200324"
  },
  {
    "id": "C0749420",
    "id2": "MedGen UID:155447",
    "medgen_label": "Thyroid agenesis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155447",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019855",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019855",
    "nando_id": "NANDO:2200331"
  },
  {
    "id": "C1384514",
    "id2": "MedGen UID:278002",
    "medgen_label": "Primary aldosteronism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/278002",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001422",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001422",
    "nando_id": "NANDO:2200361"
  },
  {
    "id": "C1841972",
    "id2": "MedGen UID:333960",
    "medgen_label": "Glucocorticoid resistance",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/333960",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014421",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014421",
    "nando_id": "NANDO:2200358"
  },
  {
    "id": "C0033805",
    "id2": "MedGen UID:18721",
    "medgen_label": "Pseudohypoaldosteronism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/18721",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018638",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018638",
    "nando_id": "NANDO:2200367"
  },
  {
    "id": "C0033806",
    "id2": "MedGen UID:46178",
    "medgen_label": "Pseudohypoparathyroidism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/46178",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019992",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019992",
    "nando_id": "NANDO:2200349"
  },
  {
    "id": "C0033835",
    "id2": "MedGen UID:10995",
    "medgen_label": "Pseudopseudohypoparathyroidism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10995",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012912",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012912",
    "nando_id": "NANDO:2200348"
  },
  {
    "id": "C0034088",
    "id2": "MedGen UID:11031",
    "medgen_label": "Pulmonary valve insufficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/11031",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001927",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001927",
    "nando_id": "NANDO:2200305"
  },
  {
    "id": "C0034089",
    "id2": "MedGen UID:18768",
    "medgen_label": "Pulmonary valve stenosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/18768",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006936",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006936",
    "nando_id": "NANDO:2200304"
  },
  {
    "id": "C0271623",
    "id2": "MedGen UID:82883",
    "medgen_label": "Hypogonadotropic hypogonadism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82883",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018555",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018555",
    "nando_id": "NANDO:2200382"
  },
  {
    "id": "C2919755",
    "id2": "MedGen UID:754060",
    "medgen_label": "Testicular dysgenesis syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/754060",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005437",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005437",
    "nando_id": "NANDO:2200383"
  },
  {
    "id": "C4318479",
    "id2": "MedGen UID:1384226",
    "medgen_label": "Growth hormone insensitivity syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1384226",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015892",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015892",
    "nando_id": "NANDO:2200321"
  },
  {
    "id": "C0017547",
    "id2": "MedGen UID:6602",
    "medgen_label": "Gigantism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6602",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020479",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020479",
    "nando_id": "NANDO:2200314"
  },
  {
    "id": "C0018213",
    "id2": "MedGen UID:6677",
    "medgen_label": "Graves disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6677",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005364",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005364",
    "nando_id": "NANDO:2200328"
  },
  {
    "id": "C0020502",
    "id2": "MedGen UID:6967",
    "medgen_label": "Hyperparathyroidism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6967",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001741",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001741",
    "nando_id": "NANDO:2200343"
  },
  {
    "id": "C0020514",
    "id2": "MedGen UID:5698",
    "medgen_label": "Hyperprolactinemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5698",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005804",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005804",
    "nando_id": "NANDO:2200322"
  },
  {
    "id": "C0020550",
    "id2": "MedGen UID:6972",
    "medgen_label": "Hyperthyroidism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6972",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0004425",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004425",
    "nando_id": "NANDO:2200329"
  },
  {
    "id": "C0020626",
    "id2": "MedGen UID:6985",
    "medgen_label": "Hypoparathyroidism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6985",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001220",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001220",
    "nando_id": "NANDO:2200345"
  },
  {
    "id": "C0021141",
    "id2": "MedGen UID:5772",
    "medgen_label": "Inappropriate antidiuretic hormone secretion",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5772",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006802",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006802",
    "nando_id": "NANDO:2200323"
  },
  {
    "id": "C0238183",
    "id2": "MedGen UID:536775",
    "medgen_label": "Atrophic thyroiditis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/536775",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005624",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005624",
    "nando_id": "NANDO:2200336"
  },
  {
    "id": "C1449844",
    "id2": "MedGen UID:259599",
    "medgen_label": "Pseudohypoaldosteronism, type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/259599",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019162",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019162",
    "nando_id": "NANDO:2200369"
  },
  {
    "id": "C5679572",
    "id2": "MedGen UID:1843308",
    "medgen_label": "Isolated congenital growth hormone deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1843308",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000050",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000050",
    "nando_id": "NANDO:2200317"
  },
  {
    "id": "C5679613",
    "id2": "MedGen UID:1814438",
    "medgen_label": "46,XX ovotesticular disorder of sex development",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1814438",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016281",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016281",
    "nando_id": "NANDO:2200387"
  },
  {
    "id": "C5680091",
    "id2": "MedGen UID:1842250",
    "medgen_label": "Non-acquired combined pituitary hormone deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1842250",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018762",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018762",
    "nando_id": "NANDO:2200312"
  },
  {
    "id": "C5680513",
    "id2": "MedGen UID:1842596",
    "medgen_label": "Peripheral precocious puberty",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1842596",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015791",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015791",
    "nando_id": "NANDO:2200378"
  },
  {
    "id": "C5681569",
    "id2": "MedGen UID:1843262",
    "medgen_label": "Acquired pituitary hormone deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1843262",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019832",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019832",
    "nando_id": "NANDO:2200313"
  },
  {
    "id": "C1850568",
    "id2": "MedGen UID:376827",
    "medgen_label": "Proteosome-associated autoinflammatory syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/376827",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009726",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009726",
    "nando_id": "NANDO:2200435"
  },
  {
    "id": "C1852093",
    "id2": "MedGen UID:377589",
    "medgen_label": "Maturity-onset diabetes of the young type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/377589",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0007452",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007452",
    "nando_id": "NANDO:2200461"
  },
  {
    "id": "C0003509",
    "id2": "MedGen UID:8154",
    "medgen_label": "Aortitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/8154",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0006656",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006656",
    "nando_id": "NANDO:2200423"
  },
  {
    "id": "C0004943",
    "id2": "MedGen UID:2568",
    "medgen_label": "Behcet disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/2568",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007191",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007191",
    "nando_id": "NANDO:2200422"
  },
  {
    "id": "C0007095",
    "id2": "MedGen UID:2838",
    "medgen_label": "Carcinoid tumor",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/2838",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0005369",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005369",
    "nando_id": "NANDO:2200396"
  },
  {
    "id": "C0008029",
    "id2": "MedGen UID:40219",
    "medgen_label": "Fibrous dysplasia of jaw",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/40219",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007315",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007315",
    "nando_id": "NANDO:2200444"
  },
  {
    "id": "C0008728",
    "id2": "MedGen UID:3088",
    "medgen_label": "Eosinophilic granulomatosis with polyangiitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/3088",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015943",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015943",
    "nando_id": "NANDO:2200427"
  },
  {
    "id": "C0410422",
    "id2": "MedGen UID:140822",
    "medgen_label": "Chronic multifocal osteomyelitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/140822",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009813",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009813",
    "nando_id": "NANDO:2200438"
  },
  {
    "id": "C2673198",
    "id2": "MedGen UID:435869",
    "medgen_label": "Familial cold autoinflammatory syndrome 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/435869",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012724",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012724",
    "nando_id": "NANDO:2200449"
  },
  {
    "id": "C2675508",
    "id2": "MedGen UID:393403",
    "medgen_label": "Inflammatory bowel disease 25",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/393403",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012941",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012941",
    "nando_id": "NANDO:2200448"
  },
  {
    "id": "C0023787",
    "id2": "MedGen UID:6111",
    "medgen_label": "Lipodystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6111",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006573",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006573",
    "nando_id": "NANDO:2200404"
  },
  {
    "id": "C0024141",
    "id2": "MedGen UID:6146",
    "medgen_label": "Systemic lupus erythematosus",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6146",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007915",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007915",
    "nando_id": "NANDO:2200416"
  },
  {
    "id": "C0025267",
    "id2": "MedGen UID:9957",
    "medgen_label": "Multiple endocrine neoplasia, type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9957",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007540",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007540",
    "nando_id": "NANDO:2200405"
  },
  {
    "id": "C0025268",
    "id2": "MedGen UID:9958",
    "medgen_label": "Multiple endocrine neoplasia type 2A",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9958",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0008234",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008234",
    "nando_id": "NANDO:2200406"
  },
  {
    "id": "C0026272",
    "id2": "MedGen UID:10069",
    "medgen_label": "Mixed connective tissue disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10069",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005854",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005854",
    "nando_id": "NANDO:2200430"
  },
  {
    "id": "C0268296",
    "id2": "MedGen UID:120626",
    "medgen_label": "Testosterone 17-beta-dehydrogenase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120626",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009916",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009916",
    "nando_id": "NANDO:2200390"
  },
  {
    "id": "C0268297",
    "id2": "MedGen UID:75667",
    "medgen_label": "3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75667",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009923",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009923",
    "nando_id": "NANDO:2200389"
  },
  {
    "id": "C0392439",
    "id2": "MedGen UID:581114",
    "medgen_label": "Acrodermatitis continua suppurativa of Hallopeau",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/581114",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013626",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013626",
    "nando_id": "NANDO:2200452"
  },
  {
    "id": "C0398691",
    "id2": "MedGen UID:140768",
    "medgen_label": "Hyperimmunoglobulin D with periodic fever",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/140768",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009849",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009849",
    "nando_id": "NANDO:2200436"
  },
  {
    "id": "C1275126",
    "id2": "MedGen UID:226899",
    "medgen_label": "TNF receptor-associated periodic fever syndrome (TRAPS)",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/226899",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007727",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007727",
    "nando_id": "NANDO:2200433"
  },
  {
    "id": "C1858361",
    "id2": "MedGen UID:346801",
    "medgen_label": "Pyogenic arthritis-pyoderma gangrenosum-acne syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/346801",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011462",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011462",
    "nando_id": "NANDO:2200437"
  },
  {
    "id": "C3280914",
    "id2": "MedGen UID:482544",
    "medgen_label": "Familial cold autoinflammatory syndrome 3",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/482544",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013766",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013766",
    "nando_id": "NANDO:2200455"
  },
  {
    "id": "C3495559",
    "id2": "MedGen UID:760659",
    "medgen_label": "Juvenile idiopathic arthritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/760659",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011429",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011429",
    "nando_id": "NANDO:2200415"
  },
  {
    "id": "C3495801",
    "id2": "MedGen UID:811223",
    "medgen_label": "Granulomatosis with polyangiitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/811223",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012105",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012105",
    "nando_id": "NANDO:2200424"
  },
  {
    "id": "C3553961",
    "id2": "MedGen UID:766875",
    "medgen_label": "Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/766875",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013944",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013944",
    "nando_id": "NANDO:2200442"
  },
  {
    "id": "C3553961",
    "id2": "MedGen UID:766875",
    "medgen_label": "Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/766875",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0013944",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013944",
    "nando_id": "NANDO:2200451"
  },
  {
    "id": "C5201146",
    "id2": "MedGen UID:1684759",
    "medgen_label": "Blau syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1684759",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008523",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008523",
    "nando_id": "NANDO:2200434"
  },
  {
    "id": "C3887654",
    "id2": "MedGen UID:854497",
    "medgen_label": "Vasculitis due to ADA2 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/854497",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0014306",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014306",
    "nando_id": "NANDO:2200450"
  },
  {
    "id": "C3887654",
    "id2": "MedGen UID:854497",
    "medgen_label": "Vasculitis due to ADA2 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/854497",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014306",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014306",
    "nando_id": "NANDO:2200441"
  },
  {
    "id": "C0032460",
    "id2": "MedGen UID:10836",
    "medgen_label": "Polycystic ovaries",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10836",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008487",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008487",
    "nando_id": "NANDO:2200409"
  },
  {
    "id": "C0032897",
    "id2": "MedGen UID:46057",
    "medgen_label": "Prader-Willi syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/46057",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008300",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008300",
    "nando_id": "NANDO:2200411"
  },
  {
    "id": "C0036421",
    "id2": "MedGen UID:19897",
    "medgen_label": "Systemic sclerosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/19897",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005100",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005100",
    "nando_id": "NANDO:2200429"
  },
  {
    "id": "C1864445",
    "id2": "MedGen UID:400532",
    "medgen_label": "H syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/400532",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011273",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011273",
    "nando_id": "NANDO:2200457"
  },
  {
    "id": "C1864497",
    "id2": "MedGen UID:351141",
    "medgen_label": "Psoriasis 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/351141",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011269",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011269",
    "nando_id": "NANDO:2200443"
  },
  {
    "id": "C1864903",
    "id2": "MedGen UID:351247",
    "medgen_label": "Hyperinsulinemic hypoglycemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/351247",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005803",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005803",
    "nando_id": "NANDO:2200399"
  },
  {
    "id": "C1864997",
    "id2": "MedGen UID:351273",
    "medgen_label": "Majeed syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/351273",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012316",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012316",
    "nando_id": "NANDO:2200453"
  },
  {
    "id": "C2748507",
    "id2": "MedGen UID:411230",
    "medgen_label": "Sterile multifocal osteomyelitis with periostitis and pustulosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/411230",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013021",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013021",
    "nando_id": "NANDO:2200439"
  },
  {
    "id": "C2751053",
    "id2": "MedGen UID:442630",
    "medgen_label": "Inflammatory bowel disease 28",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/442630",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013153",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013153",
    "nando_id": "NANDO:2200447"
  },
  {
    "id": "C0017150",
    "id2": "MedGen UID:6551",
    "medgen_label": "Gastrin-producing neuroendocrine tumor",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6551",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0003523",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003523",
    "nando_id": "NANDO:2200395"
  },
  {
    "id": "C0018055",
    "id2": "MedGen UID:6654",
    "medgen_label": "Mixed gonadal dysgenesis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6654",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001969",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001969",
    "nando_id": "NANDO:2200388"
  },
  {
    "id": "C0263666",
    "id2": "MedGen UID:120486",
    "medgen_label": "Childhood type dermatomyositis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120486",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008054",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008054",
    "nando_id": "NANDO:2200418"
  },
  {
    "id": "C0752166",
    "id2": "MedGen UID:156019",
    "medgen_label": "Bardet-Biedl syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/156019",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015229",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015229",
    "nando_id": "NANDO:2200414"
  },
  {
    "id": "C1527336",
    "id2": "MedGen UID:282890",
    "medgen_label": "Sjogren syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/282890",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010030",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010030",
    "nando_id": "NANDO:2200420"
  },
  {
    "id": "CN279762",
    "id2": "MedGen UID:963057",
    "medgen_label": "45,X/46,XY mixed gonadal dysgenesis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/963057",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0015779",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015779",
    "nando_id": "NANDO:2200388"
  },
  {
    "id": "C1704375",
    "id2": "MedGen UID:309957",
    "medgen_label": "Hypophosphatemic rickets",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/309957",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0024300",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0024300",
    "nando_id": "NANDO:2200402"
  },
  {
    "id": "C1704375",
    "id2": "MedGen UID:309957",
    "medgen_label": "Hypophosphatemic rickets",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/309957",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0024300",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0024300",
    "nando_id": "NANDO:2200403"
  },
  {
    "id": "C0011993",
    "id2": "MedGen UID:41532",
    "medgen_label": "VIPoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/41532",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019960",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019960",
    "nando_id": "NANDO:2200394"
  },
  {
    "id": "C0221468",
    "id2": "MedGen UID:526251",
    "medgen_label": "Vitamin D-dependent rickets",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/526251",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0024299",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0024299",
    "nando_id": "NANDO:2200401"
  },
  {
    "id": "C2316212",
    "id2": "MedGen UID:412215",
    "medgen_label": "Cryopyrin associated periodic syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/412215",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016168",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016168",
    "nando_id": "NANDO:2200432"
  },
  {
    "id": "C2347126",
    "id2": "MedGen UID:389393",
    "medgen_label": "Microscopic polyangiitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/389393",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019124",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019124",
    "nando_id": "NANDO:2200426"
  },
  {
    "id": "C0028326",
    "id2": "MedGen UID:18073",
    "medgen_label": "Noonan syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/18073",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018997",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018997",
    "nando_id": "NANDO:2200413"
  },
  {
    "id": "C0031036",
    "id2": "MedGen UID:14681",
    "medgen_label": "Polyarteritis nodosa",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/14681",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019170",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019170",
    "nando_id": "NANDO:2200425"
  },
  {
    "id": "C0031069",
    "id2": "MedGen UID:45811",
    "medgen_label": "Familial Mediterranean fever",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/45811",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018088",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018088",
    "nando_id": "NANDO:2200431"
  },
  {
    "id": "C3826988",
    "id2": "MedGen UID:819736",
    "medgen_label": "Juvenile polymyositis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/819736",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019734",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019734",
    "nando_id": "NANDO:2200419"
  },
  {
    "id": "C4749850",
    "id2": "MedGen UID:1661450",
    "medgen_label": "Immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1661450",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016542",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016542",
    "nando_id": "NANDO:2200446"
  },
  {
    "id": "C0342731",
    "id2": "MedGen UID:87453",
    "medgen_label": "Deficiency of mevalonate kinase",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/87453",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017708",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017708",
    "nando_id": "NANDO:2200436"
  },
  {
    "id": "C0343068",
    "id2": "MedGen UID:137986",
    "medgen_label": "Familial cold autoinflammatory syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/137986",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018768",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018768",
    "nando_id": "NANDO:2200449"
  },
  {
    "id": "C3888018",
    "id2": "MedGen UID:854723",
    "medgen_label": "Familial hyperinsulinism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/854723",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0017182",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017182",
    "nando_id": "NANDO:2200399"
  },
  {
    "id": "C0032453",
    "id2": "MedGen UID:45995",
    "medgen_label": "Relapsing polychondritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/45995",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019125",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019125",
    "nando_id": "NANDO:2200428"
  },
  {
    "id": "C0039263",
    "id2": "MedGen UID:21458",
    "medgen_label": "Takayasu arteritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21458",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017991",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017991",
    "nando_id": "NANDO:2200423"
  },
  {
    "id": "C0039585",
    "id2": "MedGen UID:21102",
    "medgen_label": "Androgen resistance syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21102",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019154",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019154",
    "nando_id": "NANDO:2200391"
  },
  {
    "id": "C0041408",
    "id2": "MedGen UID:21734",
    "medgen_label": "Turner syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21734",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019499",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019499",
    "nando_id": "NANDO:2200410"
  },
  {
    "id": "C2751824",
    "id2": "MedGen UID:414114",
    "medgen_label": "46,XY disorder of sex development",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/414114",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020040",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020040",
    "nando_id": "NANDO:2200393"
  },
  {
    "id": "C0017689",
    "id2": "MedGen UID:4908",
    "medgen_label": "Glucagonoma syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/4908",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019959",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019959",
    "nando_id": "NANDO:2200397"
  },
  {
    "id": "C0021670",
    "id2": "MedGen UID:43907",
    "medgen_label": "Pancreatic insulinoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/43907",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0024677",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0024677",
    "nando_id": "NANDO:2200398"
  },
  {
    "id": "C0242292",
    "id2": "MedGen UID:69164",
    "medgen_label": "McCune-Albright syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/69164",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018919",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018919",
    "nando_id": "NANDO:2200412"
  },
  {
    "id": "C4048306",
    "id2": "MedGen UID:887211",
    "medgen_label": "Multiple endocrine neoplasia, type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/887211",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019003",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019003",
    "nando_id": "NANDO:2200406"
  },
  {
    "id": "CN262437",
    "id2": "MedGen UID:945467",
    "medgen_label": "Berardinelli-Seip congenital lipodystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/945467",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018883",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018883",
    "nando_id": "NANDO:2200465"
  },
  {
    "id": "CN294825",
    "id2": "MedGen UID:978099",
    "medgen_label": "A20 haploinsufficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/978099",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0100222",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0100222",
    "nando_id": "NANDO:2200458"
  },
  {
    "id": "C0011854",
    "id2": "MedGen UID:41522",
    "medgen_label": "Diabetes mellitus type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/41522",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005147",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005147",
    "nando_id": "NANDO:2200460"
  },
  {
    "id": "C0011859",
    "id2": "MedGen UID:4256",
    "medgen_label": "Lipoatrophic diabetes",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/4256",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005827",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005827",
    "nando_id": "NANDO:2200465"
  },
  {
    "id": "C0011860",
    "id2": "MedGen UID:41523",
    "medgen_label": "Type 2 diabetes mellitus",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/41523",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005148",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005148",
    "nando_id": "NANDO:2200461"
  },
  {
    "id": "C0158981",
    "id2": "MedGen UID:57645",
    "medgen_label": "Neonatal diabetes mellitus",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/57645",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016391",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016391",
    "nando_id": "NANDO:2200463"
  },
  {
    "id": "C0031485",
    "id2": "MedGen UID:19244",
    "medgen_label": "Phenylketonuria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/19244",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009861",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009861",
    "nando_id": "NANDO:2200467"
  },
  {
    "id": "C0268490",
    "id2": "MedGen UID:75688",
    "medgen_label": "Tyrosinemia type I",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75688",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010161",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010161",
    "nando_id": "NANDO:2200468"
  },
  {
    "id": "C0342276",
    "id2": "MedGen UID:87433",
    "medgen_label": "Maturity onset diabetes mellitus in young",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/87433",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018911",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018911",
    "nando_id": "NANDO:2200462"
  },
  {
    "id": "C4015067",
    "id2": "MedGen UID:863504",
    "medgen_label": "Periodic fever-infantile enterocolitis-autoinflammatory syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/863504",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014472",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014472",
    "nando_id": "NANDO:2200459"
  },
  {
    "id": "C0002066",
    "id2": "MedGen UID:1413",
    "medgen_label": "Alkaptonuria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1413",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008753",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008753",
    "nando_id": "NANDO:2200504"
  },
  {
    "id": "C0010691",
    "id2": "MedGen UID:8226",
    "medgen_label": "Cystinuria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/8226",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009067",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009067",
    "nando_id": "NANDO:2200489"
  },
  {
    "id": "C0220710",
    "id2": "MedGen UID:65086",
    "medgen_label": "Medium-chain acyl-coenzyme A dehydrogenase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/65086",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008721",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008721",
    "nando_id": "NANDO:2200513"
  },
  {
    "id": "C0023786",
    "id2": "MedGen UID:44171",
    "medgen_label": "Mucopolysaccharidosis type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44171",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001586",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001586",
    "nando_id": "NANDO:2200547"
  },
  {
    "id": "C0268532",
    "id2": "MedGen UID:120647",
    "medgen_label": "Prolidase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120647",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008221",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008221",
    "nando_id": "NANDO:2200472"
  },
  {
    "id": "C0268547",
    "id2": "MedGen UID:78687",
    "medgen_label": "Argininosuccinate lyase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78687",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008815",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008815",
    "nando_id": "NANDO:2200481"
  },
  {
    "id": "C0268548",
    "id2": "MedGen UID:78688",
    "medgen_label": "Arginase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78688",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008814",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008814",
    "nando_id": "NANDO:2200482"
  },
  {
    "id": "C0268583",
    "id2": "MedGen UID:120654",
    "medgen_label": "Methylmalonic acidemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120654",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002012",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002012",
    "nando_id": "NANDO:2200491"
  },
  {
    "id": "C0268647",
    "id2": "MedGen UID:75704",
    "medgen_label": "Lysinuric protein intolerance",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75704",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009109",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009109",
    "nando_id": "NANDO:2200488"
  },
  {
    "id": "C4721769",
    "id2": "MedGen UID:1648491",
    "medgen_label": "Citrullinemia type I",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1648491",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008988",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008988",
    "nando_id": "NANDO:2200480"
  },
  {
    "id": "C0342783",
    "id2": "MedGen UID:90998",
    "medgen_label": "Deficiency of butyryl-CoA dehydrogenase",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/90998",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008722",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008722",
    "nando_id": "NANDO:2200514"
  },
  {
    "id": "C0342788",
    "id2": "MedGen UID:90999",
    "medgen_label": "Renal carnitine transport defect",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/90999",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008919",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008919",
    "nando_id": "NANDO:2200508"
  },
  {
    "id": "C0342791",
    "id2": "MedGen UID:91000",
    "medgen_label": "Carnitine acylcarnitine translocase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/91000",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008918",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008918",
    "nando_id": "NANDO:2200511"
  },
  {
    "id": "C3887523",
    "id2": "MedGen UID:854382",
    "medgen_label": "Very long chain acyl-CoA dehydrogenase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/854382",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008723",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008723",
    "nando_id": "NANDO:2200512"
  },
  {
    "id": "C0016751",
    "id2": "MedGen UID:42105",
    "medgen_label": "Hereditary fructosuria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/42105",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009249",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009249",
    "nando_id": "NANDO:2200531"
  },
  {
    "id": "C0017920",
    "id2": "MedGen UID:6640",
    "medgen_label": "Glycogen storage disease, type I",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6640",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002413",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002413",
    "nando_id": "NANDO:2200538"
  },
  {
    "id": "C0019880",
    "id2": "MedGen UID:42485",
    "medgen_label": "Homocystinuria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/42485",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0004737",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0004737",
    "nando_id": "NANDO:2200474"
  },
  {
    "id": "C0020501",
    "id2": "MedGen UID:5697",
    "medgen_label": "Primary hyperoxaluria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5697",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002474",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002474",
    "nando_id": "NANDO:2200503"
  },
  {
    "id": "C1536500",
    "id2": "MedGen UID:280689",
    "medgen_label": "Deficiency of acetyl-CoA acetyltransferase",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/280689",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008760",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008760",
    "nando_id": "NANDO:2200493"
  },
  {
    "id": "C4048705",
    "id2": "MedGen UID:887708",
    "medgen_label": "Hypermethioninemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/887708",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000351",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000351",
    "nando_id": "NANDO:2200475"
  },
  {
    "id": "C1829703",
    "id2": "MedGen UID:316820",
    "medgen_label": "Carnitine palmitoyl transferase 1A deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/316820",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009705",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009705",
    "nando_id": "NANDO:2200509"
  },
  {
    "id": "C0162671",
    "id2": "MedGen UID:56485",
    "medgen_label": "Juvenile myopathy, encephalopathy, lactic acidosis AND stroke",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/56485",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010789",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010789",
    "nando_id": "NANDO:2200525"
  },
  {
    "id": "C0162672",
    "id2": "MedGen UID:56486",
    "medgen_label": "MERRF syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/56486",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010790",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010790",
    "nando_id": "NANDO:2200526"
  },
  {
    "id": "C1997910",
    "id2": "MedGen UID:372684",
    "medgen_label": "Citrin deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/372684",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016602",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016602",
    "nando_id": "NANDO:2200483"
  },
  {
    "id": "C0023264",
    "id2": "MedGen UID:44095",
    "medgen_label": "Leigh syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44095",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009723",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009723",
    "nando_id": "NANDO:2200527"
  },
  {
    "id": "C0024776",
    "id2": "MedGen UID:6217",
    "medgen_label": "Maple syrup urine disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6217",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009563",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009563",
    "nando_id": "NANDO:2200473"
  },
  {
    "id": "C0026755",
    "id2": "MedGen UID:10119",
    "medgen_label": "Multiple carboxylase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10119",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015454",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015454",
    "nando_id": "NANDO:2200500"
  },
  {
    "id": "C0268151",
    "id2": "MedGen UID:82777",
    "medgen_label": "Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82777",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009258",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009258",
    "nando_id": "NANDO:2200532"
  },
  {
    "id": "C0268155",
    "id2": "MedGen UID:120614",
    "medgen_label": "Deficiency of galactokinase",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120614",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009255",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009255",
    "nando_id": "NANDO:2200533"
  },
  {
    "id": "C0268194",
    "id2": "MedGen UID:120618",
    "medgen_label": "Phosphoenolpyruvate carboxykinase (GTP) deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120618",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017320",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017320",
    "nando_id": "NANDO:2200536"
  },
  {
    "id": "C0268418",
    "id2": "MedGen UID:82803",
    "medgen_label": "Inborn glycerol kinase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82803",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010613",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010613",
    "nando_id": "NANDO:2200505"
  },
  {
    "id": "C0268487",
    "id2": "MedGen UID:75687",
    "medgen_label": "Tyrosinemia type II",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75687",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010160",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010160",
    "nando_id": "NANDO:2200469"
  },
  {
    "id": "C0268540",
    "id2": "MedGen UID:82815",
    "medgen_label": "Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82815",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009393",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009393",
    "nando_id": "NANDO:2200485"
  },
  {
    "id": "C0268542",
    "id2": "MedGen UID:75692",
    "medgen_label": "Ornithine carbamoyltransferase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75692",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010703",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010703",
    "nando_id": "NANDO:2200479"
  },
  {
    "id": "C0268543",
    "id2": "MedGen UID:120649",
    "medgen_label": "Hyperammonemia, type III",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120649",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009377",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009377",
    "nando_id": "NANDO:2200477"
  },
  {
    "id": "C0268575",
    "id2": "MedGen UID:82822",
    "medgen_label": "Isovaleryl-CoA dehydrogenase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82822",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009475",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009475",
    "nando_id": "NANDO:2200494"
  },
  {
    "id": "C0268579",
    "id2": "MedGen UID:75694",
    "medgen_label": "Propionic acidemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75694",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011628",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011628",
    "nando_id": "NANDO:2200492"
  },
  {
    "id": "C0268595",
    "id2": "MedGen UID:124337",
    "medgen_label": "Glutaric aciduria, type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/124337",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009281",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009281",
    "nando_id": "NANDO:2200501"
  },
  {
    "id": "C0268596",
    "id2": "MedGen UID:75696",
    "medgen_label": "Multiple acyl-CoA dehydrogenase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75696",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009282",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009282",
    "nando_id": "NANDO:2200502"
  },
  {
    "id": "C0268601",
    "id2": "MedGen UID:78692",
    "medgen_label": "Deficiency of hydroxymethylglutaryl-CoA lyase",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78692",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009520",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009520",
    "nando_id": "NANDO:2200497"
  },
  {
    "id": "C0268623",
    "id2": "MedGen UID:78694",
    "medgen_label": "Tyrosinemia type III",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78694",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010162",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010162",
    "nando_id": "NANDO:2200470"
  },
  {
    "id": "C1855861",
    "id2": "MedGen UID:343430",
    "medgen_label": "Glycogen storage disorder due to hepatic glycogen synthase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/343430",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009414",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009414",
    "nando_id": "NANDO:2200537"
  },
  {
    "id": "C3696376",
    "id2": "MedGen UID:777186",
    "medgen_label": "3-Methylglutaconic aciduria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/777186",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017359",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017359",
    "nando_id": "NANDO:2200496"
  },
  {
    "id": "C4082171",
    "id2": "MedGen UID:907954",
    "medgen_label": "Congenital hyperammonemia, type I",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/907954",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009376",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009376",
    "nando_id": "NANDO:2200478"
  },
  {
    "id": "C0342770",
    "id2": "MedGen UID:87458",
    "medgen_label": "Fumarase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/87458",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011730",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011730",
    "nando_id": "NANDO:2200520"
  },
  {
    "id": "C0342782",
    "id2": "MedGen UID:452449",
    "medgen_label": "Mitochondrial DNA depletion syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/452449",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018158",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018158",
    "nando_id": "NANDO:2200528"
  },
  {
    "id": "C0342782",
    "id2": "MedGen UID:452449",
    "medgen_label": "Mitochondrial DNA depletion syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/452449",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018158",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018158",
    "nando_id": "NANDO:2200523"
  },
  {
    "id": "C0342790",
    "id2": "MedGen UID:137978",
    "medgen_label": "Carnitine palmitoyltransferase II deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/137978",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0015515",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015515",
    "nando_id": "NANDO:2200510"
  },
  {
    "id": "C0342792",
    "id2": "MedGen UID:137979",
    "medgen_label": "Succinyl-CoA acetoacetate transferase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/137979",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009492",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009492",
    "nando_id": "NANDO:2200499"
  },
  {
    "id": "C4551505",
    "id2": "MedGen UID:1633312",
    "medgen_label": "Methylcrotonyl-CoA carboxylase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1633312",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018950",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018950",
    "nando_id": "NANDO:2200495"
  },
  {
    "id": "C4551966",
    "id2": "MedGen UID:1645412",
    "medgen_label": "Encephalopathy due to GLUT1 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1645412",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011724",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011724",
    "nando_id": "NANDO:2200545"
  },
  {
    "id": "C0034341",
    "id2": "MedGen UID:18801",
    "medgen_label": "Pyruvate carboxylase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/18801",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009949",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009949",
    "nando_id": "NANDO:2200519"
  },
  {
    "id": "C1969443",
    "id2": "MedGen UID:370665",
    "medgen_label": "Mitochondrial trifunctional protein deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/370665",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012172",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012172",
    "nando_id": "NANDO:2200515"
  },
  {
    "id": "C2751532",
    "id2": "MedGen UID:414399",
    "medgen_label": "3-hydroxy-3-methylglutaryl-CoA synthase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/414399",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011614",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011614",
    "nando_id": "NANDO:2200498"
  },
  {
    "id": "C0016756",
    "id2": "MedGen UID:42106",
    "medgen_label": "Fructose-biphosphatase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/42106",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009251",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009251",
    "nando_id": "NANDO:2200535"
  },
  {
    "id": "C0017922",
    "id2": "MedGen UID:6641",
    "medgen_label": "Glycogen storage disease type III",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6641",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009291",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009291",
    "nando_id": "NANDO:2200539"
  },
  {
    "id": "C0017923",
    "id2": "MedGen UID:6642",
    "medgen_label": "Glycogen storage disease, type IV",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6642",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009292",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009292",
    "nando_id": "NANDO:2200540"
  },
  {
    "id": "C0017924",
    "id2": "MedGen UID:5341",
    "medgen_label": "Glycogen storage disease, type V",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5341",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009293",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009293",
    "nando_id": "NANDO:2200541"
  },
  {
    "id": "C0017925",
    "id2": "MedGen UID:6643",
    "medgen_label": "Glycogen storage disease, type VI",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6643",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009294",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009294",
    "nando_id": "NANDO:2200542"
  },
  {
    "id": "C0017926",
    "id2": "MedGen UID:5342",
    "medgen_label": "Glycogen storage disease, type VII",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5342",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009295",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009295",
    "nando_id": "NANDO:2200543"
  },
  {
    "id": "C0018425",
    "id2": "MedGen UID:6695",
    "medgen_label": "Ornithine aminotransferase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6695",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009796",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009796",
    "nando_id": "NANDO:2200486"
  },
  {
    "id": "C0018425",
    "id2": "MedGen UID:6695",
    "medgen_label": "Ornithine aminotransferase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6695",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009796",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009796",
    "nando_id": "NANDO:2200484"
  },
  {
    "id": "C0018609",
    "id2": "MedGen UID:6723",
    "medgen_label": "Neutral 1 amino acid transport defect",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6723",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009324",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009324",
    "nando_id": "NANDO:2200487"
  },
  {
    "id": "C0022541",
    "id2": "MedGen UID:9618",
    "medgen_label": "Kearns-Sayre syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9618",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010787",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010787",
    "nando_id": "NANDO:2200529"
  },
  {
    "id": "C0751161",
    "id2": "MedGen UID:199598",
    "medgen_label": "UDPglucose-4-epimerase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/199598",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009257",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009257",
    "nando_id": "NANDO:2200534"
  },
  {
    "id": "C0751748",
    "id2": "MedGen UID:155625",
    "medgen_label": "Non-ketotic hyperglycinemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155625",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011612",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011612",
    "nando_id": "NANDO:2200476"
  },
  {
    "id": "C0268528",
    "id2": "MedGen UID:75690",
    "medgen_label": "Hyperprolinemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75690",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0023419",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0023419",
    "nando_id": "NANDO:2200471"
  },
  {
    "id": "C0400973",
    "id2": "MedGen UID:98324",
    "medgen_label": "Inborn disorder of bile acid synthesis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/98324",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019218",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019218",
    "nando_id": "NANDO:2200506"
  },
  {
    "id": "C0034345",
    "id2": "MedGen UID:19610",
    "medgen_label": "Pyruvate dehydrogenase complex deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/19610",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019169",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019169",
    "nando_id": "NANDO:2200518"
  },
  {
    "id": "C0023522",
    "id2": "MedGen UID:6071",
    "medgen_label": "Metachromatic leukodystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6071",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018868",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018868",
    "nando_id": "NANDO:2200560"
  },
  {
    "id": "C0026705",
    "id2": "MedGen UID:7734",
    "medgen_label": "Mucopolysaccharidosis, MPS-II",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7734",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010674",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010674",
    "nando_id": "NANDO:2200548"
  },
  {
    "id": "C0026706",
    "id2": "MedGen UID:6452",
    "medgen_label": "Sanfilippo syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6452",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018937",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018937",
    "nando_id": "NANDO:2200549"
  },
  {
    "id": "C0026707",
    "id2": "MedGen UID:44513",
    "medgen_label": "Morquio syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44513",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018938",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018938",
    "nando_id": "NANDO:2200550"
  },
  {
    "id": "C0026709",
    "id2": "MedGen UID:44514",
    "medgen_label": "Mucopolysaccharidosis type 6",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44514",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009661",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009661",
    "nando_id": "NANDO:2200551"
  },
  {
    "id": "C0028064",
    "id2": "MedGen UID:10348",
    "medgen_label": "Sphingomyelin/cholesterol lipidosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10348",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001982",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001982",
    "nando_id": "NANDO:2200561"
  },
  {
    "id": "C0268225",
    "id2": "MedGen UID:78649",
    "medgen_label": "Aspartylglucosaminuria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78649",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008830",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008830",
    "nando_id": "NANDO:2200555"
  },
  {
    "id": "C0268226",
    "id2": "MedGen UID:120621",
    "medgen_label": "Sialidosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120621",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017734",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017734",
    "nando_id": "NANDO:2200556"
  },
  {
    "id": "C0268233",
    "id2": "MedGen UID:82779",
    "medgen_label": "Combined deficiency of sialidase AND beta galactosidase",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82779",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009737",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009737",
    "nando_id": "NANDO:2200557"
  },
  {
    "id": "C0268274",
    "id2": "MedGen UID:78656",
    "medgen_label": "GM2 gangliosidosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78656",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017720",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017720",
    "nando_id": "NANDO:2200559"
  },
  {
    "id": "C0085131",
    "id2": "MedGen UID:43107",
    "medgen_label": "GM1 gangliosidosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/43107",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018149",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018149",
    "nando_id": "NANDO:2200558"
  },
  {
    "id": "C0085132",
    "id2": "MedGen UID:43108",
    "medgen_label": "Mucopolysaccharidosis type 7",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/43108",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009662",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009662",
    "nando_id": "NANDO:2200552"
  },
  {
    "id": "C0016788",
    "id2": "MedGen UID:5288",
    "medgen_label": "Fucosidosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5288",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009254",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009254",
    "nando_id": "NANDO:2200553"
  },
  {
    "id": "C0017205",
    "id2": "MedGen UID:42164",
    "medgen_label": "Gaucher disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/42164",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018150",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018150",
    "nando_id": "NANDO:2200562"
  },
  {
    "id": "C1832200",
    "id2": "MedGen UID:330407",
    "medgen_label": "Peroxisome biogenesis disorder",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/330407",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019234",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019234",
    "nando_id": "NANDO:2200575"
  },
  {
    "id": "C0000744",
    "id2": "MedGen UID:1253",
    "medgen_label": "Abetalipoproteinaemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1253",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008692",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008692",
    "nando_id": "NANDO:2200604"
  },
  {
    "id": "C0002876",
    "id2": "MedGen UID:8064",
    "medgen_label": "Congenital dyserythropoietic anemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/8064",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019403",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019403",
    "nando_id": "NANDO:2200615"
  },
  {
    "id": "C0002888",
    "id2": "MedGen UID:1527",
    "medgen_label": "Megaloblastic anemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1527",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001700",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001700",
    "nando_id": "NANDO:2200612"
  },
  {
    "id": "C0002895",
    "id2": "MedGen UID:287",
    "medgen_label": "Hb SS disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/287",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011382",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011382",
    "nando_id": "NANDO:2200624"
  },
  {
    "id": "C0002896",
    "id2": "MedGen UID:8067",
    "medgen_label": "Sideroblastic anemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/8067",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015194",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015194",
    "nando_id": "NANDO:2200616"
  },
  {
    "id": "C0002986",
    "id2": "MedGen UID:8083",
    "medgen_label": "Fabry disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/8083",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010526",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010526",
    "nando_id": "NANDO:2200563"
  },
  {
    "id": "C0162309",
    "id2": "MedGen UID:57667",
    "medgen_label": "Adrenoleukodystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/57667",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018544",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018544",
    "nando_id": "NANDO:2200576"
  },
  {
    "id": "C0220987",
    "id2": "MedGen UID:472940",
    "medgen_label": "Hereditary orotic aciduria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/472940",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009797",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009797",
    "nando_id": "NANDO:2200590"
  },
  {
    "id": "C0220988",
    "id2": "MedGen UID:450997",
    "medgen_label": "Xanthinuria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/450997",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000721",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000721",
    "nando_id": "NANDO:2200588"
  },
  {
    "id": "C0221036",
    "id2": "MedGen UID:66355",
    "medgen_label": "Hereditary acrodermatitis enteropathica",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/66355",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008713",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008713",
    "nando_id": "NANDO:2200584"
  },
  {
    "id": "C0221757",
    "id2": "MedGen UID:67461",
    "medgen_label": "Alpha-1-antitrypsin deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/67461",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013282",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013282",
    "nando_id": "NANDO:2200611"
  },
  {
    "id": "C2673377",
    "id2": "MedGen UID:435914",
    "medgen_label": "Mucolipidosis type II",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/435914",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009650",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009650",
    "nando_id": "NANDO:2200567"
  },
  {
    "id": "C2931872",
    "id2": "MedGen UID:419512",
    "medgen_label": "Free sialic acid storage disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/419512",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019366",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019366",
    "nando_id": "NANDO:2200572"
  },
  {
    "id": "C2939465",
    "id2": "MedGen UID:473706",
    "medgen_label": "G6PD deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/473706",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005775",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005775",
    "nando_id": "NANDO:2200627"
  },
  {
    "id": "C0022716",
    "id2": "MedGen UID:44030",
    "medgen_label": "Menkes kinky-hair syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44030",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010651",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010651",
    "nando_id": "NANDO:2200580"
  },
  {
    "id": "C0023374",
    "id2": "MedGen UID:9721",
    "medgen_label": "Lesch-Nyhan syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9721",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0010298",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010298",
    "nando_id": "NANDO:2200586"
  },
  {
    "id": "C0023521",
    "id2": "MedGen UID:44131",
    "medgen_label": "Galactosylceramide beta-galactosidase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44131",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009499",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009499",
    "nando_id": "NANDO:2200564"
  },
  {
    "id": "C0023795",
    "id2": "MedGen UID:6112",
    "medgen_label": "Lipid proteinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6112",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009530",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009530",
    "nando_id": "NANDO:2200608"
  },
  {
    "id": "C0027877",
    "id2": "MedGen UID:10326",
    "medgen_label": "Neuronal ceroid lipofuscinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10326",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016295",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016295",
    "nando_id": "NANDO:2200573"
  },
  {
    "id": "C0268120",
    "id2": "MedGen UID:82772",
    "medgen_label": "Adenine phosphoribosyltransferase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82772",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013869",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013869",
    "nando_id": "NANDO:2200587"
  },
  {
    "id": "C0268255",
    "id2": "MedGen UID:78654",
    "medgen_label": "Farber lipogranulomatosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78654",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009218",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009218",
    "nando_id": "NANDO:2200565"
  },
  {
    "id": "C0268263",
    "id2": "MedGen UID:75664",
    "medgen_label": "Multiple sulfatase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75664",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010088",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010088",
    "nando_id": "NANDO:2200566"
  },
  {
    "id": "C0268353",
    "id2": "MedGen UID:82793",
    "medgen_label": "Cutis laxa, X-linked",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82793",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010572",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010572",
    "nando_id": "NANDO:2200581"
  },
  {
    "id": "C0268624",
    "id2": "MedGen UID:78695",
    "medgen_label": "Sulfite oxidase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78695",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010089",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010089",
    "nando_id": "NANDO:2200583"
  },
  {
    "id": "C0268631",
    "id2": "MedGen UID:124340",
    "medgen_label": "Succinate-semialdehyde dehydrogenase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/124340",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010083",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010083",
    "nando_id": "NANDO:2200599"
  },
  {
    "id": "C0520739",
    "id2": "MedGen UID:141708",
    "medgen_label": "Pyropoikilocytosis, hereditary",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/141708",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009948",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009948",
    "nando_id": "NANDO:2200631"
  },
  {
    "id": "C0521802",
    "id2": "MedGen UID:105489",
    "medgen_label": "Atransferrinemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/105489",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008846",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008846",
    "nando_id": "NANDO:2200617"
  },
  {
    "id": "C1260899",
    "id2": "MedGen UID:266045",
    "medgen_label": "Diamond-Blackfan anemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/266045",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015253",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015253",
    "nando_id": "NANDO:2200614"
  },
  {
    "id": "C1262483",
    "id2": "MedGen UID:490161",
    "medgen_label": "Hereditary stomatocytosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/490161",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020102",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020102",
    "nando_id": "NANDO:2200623"
  },
  {
    "id": "C1264008",
    "id2": "MedGen UID:688249",
    "medgen_label": "Cold agglutinin disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/688249",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018922",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018922",
    "nando_id": "NANDO:2200618"
  },
  {
    "id": "C1275125",
    "id2": "MedGen UID:698423",
    "medgen_label": "Inherited porphyria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/698423",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019142",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019142",
    "nando_id": "NANDO:2200610"
  },
  {
    "id": "C3713420",
    "id2": "MedGen UID:780028",
    "medgen_label": "Familial hyperaldosteronism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/780028",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0016525",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016525",
    "nando_id": "NANDO:2200602"
  },
  {
    "id": "C4707560",
    "id2": "MedGen UID:1647585",
    "medgen_label": "Adult pure red cell aplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1647585",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020338",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020338",
    "nando_id": "NANDO:2200613"
  },
  {
    "id": "C4746777",
    "id2": "MedGen UID:1648402",
    "medgen_label": "Orthostatic hypotension 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1648402",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009123",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009123",
    "nando_id": "NANDO:2200597"
  },
  {
    "id": "C0086774",
    "id2": "MedGen UID:39693",
    "medgen_label": "Paroxysmal cold hemoglobinuria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/39693",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019533",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019533",
    "nando_id": "NANDO:2200619"
  },
  {
    "id": "C0151691",
    "id2": "MedGen UID:57731",
    "medgen_label": "Decreased HDL cholesterol concentration",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/57731",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017773",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017773",
    "nando_id": "NANDO:2200605"
  },
  {
    "id": "C0340968",
    "id2": "MedGen UID:473069",
    "medgen_label": "Pyruvate kinase deficiency of red cells",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/473069",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009950",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009950",
    "nando_id": "NANDO:2200628"
  },
  {
    "id": "C0342705",
    "id2": "MedGen UID:83348",
    "medgen_label": "Congenital defect of folate absorption",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/83348",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009238",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009238",
    "nando_id": "NANDO:2200592"
  },
  {
    "id": "C0342708",
    "id2": "MedGen UID:137977",
    "medgen_label": "Gamma-aminobutyric acid transaminase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/137977",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013166",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013166",
    "nando_id": "NANDO:2200598"
  },
  {
    "id": "C0700623",
    "id2": "MedGen UID:675194",
    "medgen_label": "Familial hyperlipidemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/675194",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001336",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001336",
    "nando_id": "NANDO:2200603"
  },
  {
    "id": "C0745103",
    "id2": "MedGen UID:152875",
    "medgen_label": "Hypercholesterolemia, familial, 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/152875",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0007750",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007750",
    "nando_id": "NANDO:2200602"
  },
  {
    "id": "C0033788",
    "id2": "MedGen UID:10988",
    "medgen_label": "Pseudo-Hurler polydystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10988",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018931",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018931",
    "nando_id": "NANDO:2200568"
  },
  {
    "id": "C0034960",
    "id2": "MedGen UID:11161",
    "medgen_label": "Phytanic acid storage disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/11161",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009958",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009958",
    "nando_id": "NANDO:2200577"
  },
  {
    "id": "C0037889",
    "id2": "MedGen UID:52450",
    "medgen_label": "Hereditary spherocytosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/52450",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019350",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019350",
    "nando_id": "NANDO:2200622"
  },
  {
    "id": "C0039730",
    "id2": "MedGen UID:21121",
    "medgen_label": "Thalassemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21121",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000984",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000984",
    "nando_id": "NANDO:2200626"
  },
  {
    "id": "C0043208",
    "id2": "MedGen UID:53088",
    "medgen_label": "Wolman disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/53088",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0019148",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019148",
    "nando_id": "NANDO:2200570"
  },
  {
    "id": "C0272006",
    "id2": "MedGen UID:82893",
    "medgen_label": "Unstable hemoglobin disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82893",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020459",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020459",
    "nando_id": "NANDO:2200625"
  },
  {
    "id": "C0272051",
    "id2": "MedGen UID:124415",
    "medgen_label": "Xerocytosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/124415",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017910",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017910",
    "nando_id": "NANDO:2200633"
  },
  {
    "id": "C1867339",
    "id2": "MedGen UID:357960",
    "medgen_label": "Red cell phospholipid defect with hemolysis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/357960",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008367",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008367",
    "nando_id": "NANDO:2200634"
  },
  {
    "id": "C4316899",
    "id2": "MedGen UID:1384792",
    "medgen_label": "Cystinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1384792",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016239",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016239",
    "nando_id": "NANDO:2200571"
  },
  {
    "id": "C0013720",
    "id2": "MedGen UID:41720",
    "medgen_label": "Ehlers-Danlos syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/41720",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020066",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020066",
    "nando_id": "NANDO:2200607"
  },
  {
    "id": "C0013902",
    "id2": "MedGen UID:41747",
    "medgen_label": "Hereditary elliptocytosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/41747",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017319",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017319",
    "nando_id": "NANDO:2200630"
  },
  {
    "id": "C0017921",
    "id2": "MedGen UID:5340",
    "medgen_label": "Glycogen storage disease, type II",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5340",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009290",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009290",
    "nando_id": "NANDO:2200569"
  },
  {
    "id": "C0019021",
    "id2": "MedGen UID:6789",
    "medgen_label": "Hemoglobin C disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6789",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016242",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016242",
    "nando_id": "NANDO:2200635"
  },
  {
    "id": "C0019202",
    "id2": "MedGen UID:42426",
    "medgen_label": "Wilson disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/42426",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010200",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010200",
    "nando_id": "NANDO:2200579"
  },
  {
    "id": "C0020445",
    "id2": "MedGen UID:5688",
    "medgen_label": "Familial hypercholesterolemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5688",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005439",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005439",
    "nando_id": "NANDO:2200602"
  },
  {
    "id": "C0751436",
    "id2": "MedGen UID:199656",
    "medgen_label": "Hyperphenylalaninemia due to tetrahydrobiopterin deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/199656",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016543",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016543",
    "nando_id": "NANDO:2200594"
  },
  {
    "id": "C0878682",
    "id2": "MedGen UID:168057",
    "medgen_label": "Deficiency of ferroxidase",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/168057",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011426",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011426",
    "nando_id": "NANDO:2200582"
  },
  {
    "id": "C1291564",
    "id2": "MedGen UID:220945",
    "medgen_label": "Deficiency of aromatic-L-amino-acid decarboxylase",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/220945",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012084",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012084",
    "nando_id": "NANDO:2200596"
  },
  {
    "id": "C5700309",
    "id2": "MedGen UID:1814581",
    "medgen_label": "Tyrosine hydroxylase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1814581",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0100064",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0100064",
    "nando_id": "NANDO:2200595"
  },
  {
    "id": "CN305342",
    "id2": "MedGen UID:988564",
    "medgen_label": "Hypoxanthine-guanine phosphoribosyltransferase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/988564",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016088",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016088",
    "nando_id": "NANDO:2200586"
  },
  {
    "id": "C0002878",
    "id2": "MedGen UID:1916",
    "medgen_label": "Hemolytic anemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1916",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0003664",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003664",
    "nando_id": "NANDO:2200636"
  },
  {
    "id": "C1856143",
    "id2": "MedGen UID:383843",
    "medgen_label": "Shiga toxin-associated hemolytic uremic syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/383843",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019536",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019536",
    "nando_id": "NANDO:2200640"
  },
  {
    "id": "C0032463",
    "id2": "MedGen UID:45996",
    "medgen_label": "Acquired polycythemia vera",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/45996",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009891",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009891",
    "nando_id": "NANDO:2200643"
  },
  {
    "id": "C0020532",
    "id2": "MedGen UID:9372",
    "medgen_label": "Hypersplenism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9372",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006795",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006795",
    "nando_id": "NANDO:2200637"
  },
  {
    "id": "C0012739",
    "id2": "MedGen UID:41620",
    "medgen_label": "Disseminated intravascular coagulation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/41620",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001243",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001243",
    "nando_id": "NANDO:2200639"
  },
  {
    "id": "C1832388",
    "id2": "MedGen UID:321945",
    "medgen_label": "Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/321945",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0100083",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0100083",
    "nando_id": "NANDO:2200662"
  },
  {
    "id": "C1853278",
    "id2": "MedGen UID:344008",
    "medgen_label": "Platelet-type bleeding disorder 8",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/344008",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012354",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012354",
    "nando_id": "NANDO:2200669"
  },
  {
    "id": "C1854273",
    "id2": "MedGen UID:340183",
    "medgen_label": "Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/340183",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011555",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011555",
    "nando_id": "NANDO:2200660"
  },
  {
    "id": "C0002874",
    "id2": "MedGen UID:8063",
    "medgen_label": "Aplastic anemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/8063",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015909",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015909",
    "nando_id": "NANDO:2200693"
  },
  {
    "id": "C0005129",
    "id2": "MedGen UID:2212",
    "medgen_label": "Bernard Soulier syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/2212",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009276",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009276",
    "nando_id": "NANDO:2200656"
  },
  {
    "id": "C0008533",
    "id2": "MedGen UID:945",
    "medgen_label": "Hereditary factor IX deficiency disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/945",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010604",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010604",
    "nando_id": "NANDO:2200677"
  },
  {
    "id": "C0012236",
    "id2": "MedGen UID:4297",
    "medgen_label": "DiGeorge syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/4297",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0008564",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008564",
    "nando_id": "NANDO:2200712"
  },
  {
    "id": "C0175703",
    "id2": "MedGen UID:61235",
    "medgen_label": "Radial aplasia-thrombocytopenia syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/61235",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010121",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010121",
    "nando_id": "NANDO:2200661"
  },
  {
    "id": "C0220704",
    "id2": "MedGen UID:65085",
    "medgen_label": "Velocardiofacial syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/65085",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0008644",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008644",
    "nando_id": "NANDO:2200712"
  },
  {
    "id": "C2584774",
    "id2": "MedGen UID:749036",
    "medgen_label": "Congenital afibrinogenemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/749036",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008737",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008737",
    "nando_id": "NANDO:2200672"
  },
  {
    "id": "C2931418",
    "id2": "MedGen UID:444051",
    "medgen_label": "MHC class II deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/444051",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008855",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008855",
    "nando_id": "NANDO:2200702"
  },
  {
    "id": "C0026987",
    "id2": "MedGen UID:10146",
    "medgen_label": "Myelofibrosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10146",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0044903",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0044903",
    "nando_id": "NANDO:2200692"
  },
  {
    "id": "C0268125",
    "id2": "MedGen UID:75653",
    "medgen_label": "Purine-nucleoside phosphorylase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75653",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013171",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013171",
    "nando_id": "NANDO:2200698"
  },
  {
    "id": "C0398650",
    "id2": "MedGen UID:584986",
    "medgen_label": "Autoimmune thrombocytopenic purpura",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/584986",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008558",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008558",
    "nando_id": "NANDO:2200645"
  },
  {
    "id": "C1279481",
    "id2": "MedGen UID:220906",
    "medgen_label": "X-linked severe combined immunodeficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/220906",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010315",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010315",
    "nando_id": "NANDO:2200694"
  },
  {
    "id": "C1280798",
    "id2": "MedGen UID:226914",
    "medgen_label": "Pseudo von Willebrand disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/226914",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008332",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008332",
    "nando_id": "NANDO:2200668"
  },
  {
    "id": "C1856883",
    "id2": "MedGen UID:384006",
    "medgen_label": "Combined deficiency of factor V and factor VIII",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/384006",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018175",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018175",
    "nando_id": "NANDO:2200686"
  },
  {
    "id": "C1858266",
    "id2": "MedGen UID:346868",
    "medgen_label": "MHC class I deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/346868",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011476",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011476",
    "nando_id": "NANDO:2200701"
  },
  {
    "id": "C1861185",
    "id2": "MedGen UID:349976",
    "medgen_label": "Thrombocytopenia 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/349976",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008555",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008555",
    "nando_id": "NANDO:2200663"
  },
  {
    "id": "C1863236",
    "id2": "MedGen UID:354935",
    "medgen_label": "Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/354935",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007064",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007064",
    "nando_id": "NANDO:2200696"
  },
  {
    "id": "C3280120",
    "id2": "MedGen UID:481750",
    "medgen_label": "Platelet-type bleeding disorder 11",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/481750",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013623",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013623",
    "nando_id": "NANDO:2200670"
  },
  {
    "id": "C3554663",
    "id2": "MedGen UID:767577",
    "medgen_label": "Platelet-type bleeding disorder 15",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/767577",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014078",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014078",
    "nando_id": "NANDO:2200665"
  },
  {
    "id": "C0152264",
    "id2": "MedGen UID:57520",
    "medgen_label": "Familial erythrocytosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/57520",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001115",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001115",
    "nando_id": "NANDO:2200644"
  },
  {
    "id": "C0598221",
    "id2": "MedGen UID:671121",
    "medgen_label": "Hereditary thrombophilia due to congenital protein C deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/671121",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019145",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019145",
    "nando_id": "NANDO:2200689"
  },
  {
    "id": "C1837065",
    "id2": "MedGen UID:323058",
    "medgen_label": "Susceptibility to respiratory infections associated with CD8alpha chain mutation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/323058",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012161",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012161",
    "nando_id": "NANDO:2200699"
  },
  {
    "id": "C3854603",
    "id2": "MedGen UID:1720701",
    "medgen_label": "Fetal and neonatal alloimmune thrombocytopenia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1720701",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019415",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019415",
    "nando_id": "NANDO:2200647"
  },
  {
    "id": "C5575025",
    "id2": "MedGen UID:1809040",
    "medgen_label": "Combined immunodeficiency due to ZAP70 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1809040",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010023",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010023",
    "nando_id": "NANDO:2200700"
  },
  {
    "id": "C0034155",
    "id2": "MedGen UID:48266",
    "medgen_label": "Thrombotic thrombocytopenic purpura",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/48266",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018896",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018896",
    "nando_id": "NANDO:2200649"
  },
  {
    "id": "C0040028",
    "id2": "MedGen UID:11797",
    "medgen_label": "Essential thrombocythemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/11797",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005029",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005029",
    "nando_id": "NANDO:2200655"
  },
  {
    "id": "C0042974",
    "id2": "MedGen UID:22686",
    "medgen_label": "von Willebrand disorder",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/22686",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0024574",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0024574",
    "nando_id": "NANDO:2200682"
  },
  {
    "id": "C0043194",
    "id2": "MedGen UID:21921",
    "medgen_label": "Wiskott-Aldrich syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21921",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010518",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010518",
    "nando_id": "NANDO:2200704"
  },
  {
    "id": "C0272167",
    "id2": "MedGen UID:124417",
    "medgen_label": "Reticular dysgenesis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/124417",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009973",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009973",
    "nando_id": "NANDO:2200695"
  },
  {
    "id": "C0272282",
    "id2": "MedGen UID:78799",
    "medgen_label": "Cyclic thrombocytopenia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78799",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008556",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008556",
    "nando_id": "NANDO:2200653"
  },
  {
    "id": "C0272285",
    "id2": "MedGen UID:124423",
    "medgen_label": "Heparin-induced thrombocytopenia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/124423",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018048",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018048",
    "nando_id": "NANDO:2200648"
  },
  {
    "id": "C0272317",
    "id2": "MedGen UID:124425",
    "medgen_label": "Congenital prothrombin deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/124425",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013361",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013361",
    "nando_id": "NANDO:2200673"
  },
  {
    "id": "C0272339",
    "id2": "MedGen UID:75779",
    "medgen_label": "Prekallikrein deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75779",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0044744",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0044744",
    "nando_id": "NANDO:2200684"
  },
  {
    "id": "C0272340",
    "id2": "MedGen UID:75780",
    "medgen_label": "High molecular weight kininogen deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75780",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009234",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009234",
    "nando_id": "NANDO:2200685"
  },
  {
    "id": "C2700553",
    "id2": "MedGen UID:398130",
    "medgen_label": "Histiocytic medullary reticulosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/398130",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011338",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011338",
    "nando_id": "NANDO:2200697"
  },
  {
    "id": "C2750067",
    "id2": "MedGen UID:412870",
    "medgen_label": "Congenital plasminogen activator inhibitor type 1 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/412870",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013227",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013227",
    "nando_id": "NANDO:2200688"
  },
  {
    "id": "C2752081",
    "id2": "MedGen UID:414178",
    "medgen_label": "Alpha-2-plasmin inhibitor deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/414178",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009883",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009883",
    "nando_id": "NANDO:2200687"
  },
  {
    "id": "C4316906",
    "id2": "MedGen UID:1385982",
    "medgen_label": "Factor XIII deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1385982",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002241",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002241",
    "nando_id": "NANDO:2200681"
  },
  {
    "id": "C4317320",
    "id2": "MedGen UID:1369551",
    "medgen_label": "Factor V deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1369551",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020586",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020586",
    "nando_id": "NANDO:2200674"
  },
  {
    "id": "C4321502",
    "id2": "MedGen UID:1386956",
    "medgen_label": "Factor XI deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1386956",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020587",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020587",
    "nando_id": "NANDO:2200679"
  },
  {
    "id": "C0015503",
    "id2": "MedGen UID:8769",
    "medgen_label": "Factor VII deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/8769",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002244",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002244",
    "nando_id": "NANDO:2200675"
  },
  {
    "id": "C0015519",
    "id2": "MedGen UID:4635",
    "medgen_label": "Factor X deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/4635",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002247",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002247",
    "nando_id": "NANDO:2200678"
  },
  {
    "id": "C0015526",
    "id2": "MedGen UID:8772",
    "medgen_label": "Factor XII deficiency disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/8772",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009315",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009315",
    "nando_id": "NANDO:2200680"
  },
  {
    "id": "C0015530",
    "id2": "MedGen UID:4639",
    "medgen_label": "Hereditary factor XIII deficiency disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/4639",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018029",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018029",
    "nando_id": "NANDO:2200681"
  },
  {
    "id": "C0015625",
    "id2": "MedGen UID:41967",
    "medgen_label": "Fanconi anemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/41967",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019391",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019391",
    "nando_id": "NANDO:2200652"
  },
  {
    "id": "C0019069",
    "id2": "MedGen UID:5501",
    "medgen_label": "Hereditary factor VIII deficiency disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5501",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010602",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010602",
    "nando_id": "NANDO:2200676"
  },
  {
    "id": "C0242666",
    "id2": "MedGen UID:69229",
    "medgen_label": "Protein S deficiency disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/69229",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002304",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002304",
    "nando_id": "NANDO:2200690"
  },
  {
    "id": "C0796149",
    "id2": "MedGen UID:167107",
    "medgen_label": "SCOTT SYNDROME",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/167107",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009885",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009885",
    "nando_id": "NANDO:2200671"
  },
  {
    "id": "CN294181",
    "id2": "MedGen UID:977689",
    "medgen_label": "22q11.2 deletion syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/977689",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018923",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018923",
    "nando_id": "NANDO:2200712"
  },
  {
    "id": "CN305372",
    "id2": "MedGen UID:987194",
    "medgen_label": "Inherited prekallikrein deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/987194",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012901",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012901",
    "nando_id": "NANDO:2200684"
  },
  {
    "id": "C0004135",
    "id2": "MedGen UID:439",
    "medgen_label": "Ataxia-telangiectasia syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/439",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008840",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008840",
    "nando_id": "NANDO:2200705"
  },
  {
    "id": "C0005859",
    "id2": "MedGen UID:2685",
    "medgen_label": "Bloom syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/2685",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008876",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008876",
    "nando_id": "NANDO:2200707"
  },
  {
    "id": "C0007965",
    "id2": "MedGen UID:3347",
    "medgen_label": "Chédiak-Higashi syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/3347",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008963",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008963",
    "nando_id": "NANDO:2200724"
  },
  {
    "id": "C0009447",
    "id2": "MedGen UID:40407",
    "medgen_label": "Common variable immunodeficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/40407",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015517",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015517",
    "nando_id": "NANDO:2200717"
  },
  {
    "id": "C0221026",
    "id2": "MedGen UID:65123",
    "medgen_label": "X-linked agammaglobulinemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/65123",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010421",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010421",
    "nando_id": "NANDO:2200716"
  },
  {
    "id": "C2677792",
    "id2": "MedGen UID:394368",
    "medgen_label": "RIDDLE syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/394368",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012764",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012764",
    "nando_id": "NANDO:2200710"
  },
  {
    "id": "C0265965",
    "id2": "MedGen UID:78580",
    "medgen_label": "Dyskeratosis congenita",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78580",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015780",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015780",
    "nando_id": "NANDO:2200715"
  },
  {
    "id": "C0398788",
    "id2": "MedGen UID:140770",
    "medgen_label": "Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/140770",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000133",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000133",
    "nando_id": "NANDO:2200708"
  },
  {
    "id": "C0398791",
    "id2": "MedGen UID:140771",
    "medgen_label": "Microcephaly, normal intelligence and immunodeficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/140771",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009623",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009623",
    "nando_id": "NANDO:2200706"
  },
  {
    "id": "C0549463",
    "id2": "MedGen UID:107498",
    "medgen_label": "X-linked lymphoproliferative syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/107498",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010627",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010627",
    "nando_id": "NANDO:2200725"
  },
  {
    "id": "C1856128",
    "id2": "MedGen UID:344659",
    "medgen_label": "Hepatic veno-occlusive disease-immunodeficiency syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/344659",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009338",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009338",
    "nando_id": "NANDO:2200714"
  },
  {
    "id": "C3279824",
    "id2": "MedGen UID:481454",
    "medgen_label": "Recurrent infections associated with rare immunoglobulin isotypes deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/481454",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013576",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013576",
    "nando_id": "NANDO:2200719"
  },
  {
    "id": "C3887645",
    "id2": "MedGen UID:854488",
    "medgen_label": "Hyper-IgE syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/854488",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018037",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018037",
    "nando_id": "NANDO:2200713"
  },
  {
    "id": "C0272236",
    "id2": "MedGen UID:124420",
    "medgen_label": "Hyperimmunoglobulin M syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/124420",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0003947",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003947",
    "nando_id": "NANDO:2200718"
  },
  {
    "id": "C0272238",
    "id2": "MedGen UID:124421",
    "medgen_label": "Transient hypogammaglobulinemia of infancy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/124421",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015698",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015698",
    "nando_id": "NANDO:2200722"
  },
  {
    "id": "C0877024",
    "id2": "MedGen UID:164078",
    "medgen_label": "Schimke immuno-osseous dysplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/164078",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009458",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009458",
    "nando_id": "NANDO:2200711"
  },
  {
    "id": "C4049006",
    "id2": "MedGen UID:883982",
    "medgen_label": "Selective IgA deficiency disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/883982",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001341",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001341",
    "nando_id": "NANDO:2200720"
  },
  {
    "id": "CN301239",
    "id2": "MedGen UID:985772",
    "medgen_label": "Autoimmune lymphoproliferative syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/985772",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017979",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017979",
    "nando_id": "NANDO:2200726"
  },
  {
    "id": "C1852700",
    "id2": "MedGen UID:343867",
    "medgen_label": "C1 inhibitor deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/343867",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0007361",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007361",
    "nando_id": "NANDO:2200795"
  },
  {
    "id": "C0221023",
    "id2": "MedGen UID:65121",
    "medgen_label": "Cyclical neutropenia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/65121",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008090",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008090",
    "nando_id": "NANDO:2200746"
  },
  {
    "id": "C0041227",
    "id2": "MedGen UID:52872",
    "medgen_label": "Trypanosomiasis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/52872",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000940",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000940",
    "nando_id": "NANDO:2200774"
  },
  {
    "id": "C0272242",
    "id2": "MedGen UID:82898",
    "medgen_label": "Reduced circulating complement concentration",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82898",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0003832",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003832",
    "nando_id": "NANDO:2200776"
  },
  {
    "id": "C1846545",
    "id2": "MedGen UID:339548",
    "medgen_label": "Autoimmune lymphoproliferative syndrome type 2B",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/339548",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011804",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011804",
    "nando_id": "NANDO:2200740"
  },
  {
    "id": "C1853118",
    "id2": "MedGen UID:343974",
    "medgen_label": "Severe congenital neutropenia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/343974",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018542",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018542",
    "nando_id": "NANDO:2200745"
  },
  {
    "id": "C1853392",
    "id2": "MedGen UID:377894",
    "medgen_label": "Immunodeficiency due to CD25 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/377894",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011664",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011664",
    "nando_id": "NANDO:2200736"
  },
  {
    "id": "C0006845",
    "id2": "MedGen UID:2426",
    "medgen_label": "Chronic mucocutaneous candidiasis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/2426",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015279",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015279",
    "nando_id": "NANDO:2200764"
  },
  {
    "id": "C1970455",
    "id2": "MedGen UID:369736",
    "medgen_label": "Systemic lupus erythematosus, susceptibility to, 9",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/369736",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0012584",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012584",
    "nando_id": "NANDO:2200801"
  },
  {
    "id": "C2676232",
    "id2": "MedGen UID:436639",
    "medgen_label": "Complement component 6 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/436639",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012908",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012908",
    "nando_id": "NANDO:2200784"
  },
  {
    "id": "C2677092",
    "id2": "MedGen UID:383023",
    "medgen_label": "Pyogenic bacterial infections due to MyD88 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/383023",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012839",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012839",
    "nando_id": "NANDO:2200763"
  },
  {
    "id": "C3150275",
    "id2": "MedGen UID:461625",
    "medgen_label": "Complement component 2 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/461625",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009006",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009006",
    "nando_id": "NANDO:2200781"
  },
  {
    "id": "C3150649",
    "id2": "MedGen UID:461999",
    "medgen_label": "Syndromic multisystem autoimmune disease due to ITCH deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/461999",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013245",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013245",
    "nando_id": "NANDO:2200739"
  },
  {
    "id": "C3150902",
    "id2": "MedGen UID:462252",
    "medgen_label": "C1Q deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/462252",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013343",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013343",
    "nando_id": "NANDO:2200777"
  },
  {
    "id": "C3151062",
    "id2": "MedGen UID:462412",
    "medgen_label": "FADD-related immunodeficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/462412",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013408",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013408",
    "nando_id": "NANDO:2200741"
  },
  {
    "id": "C3151071",
    "id2": "MedGen UID:462421",
    "medgen_label": "Complement component 3 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/462421",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013417",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013417",
    "nando_id": "NANDO:2200782"
  },
  {
    "id": "C3151078",
    "id2": "MedGen UID:462428",
    "medgen_label": "Complement component C1s deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/462428",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013419",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013419",
    "nando_id": "NANDO:2200779"
  },
  {
    "id": "C3151085",
    "id2": "MedGen UID:462435",
    "medgen_label": "Immunodeficiency due to MASP-2 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/462435",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013423",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013423",
    "nando_id": "NANDO:2200793"
  },
  {
    "id": "C3151189",
    "id2": "MedGen UID:462539",
    "medgen_label": "Complement component 9 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/462539",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013445",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013445",
    "nando_id": "NANDO:2200787"
  },
  {
    "id": "C3151226",
    "id2": "MedGen UID:462576",
    "medgen_label": "Immunodeficiency due to ficolin3 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/462576",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013467",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013467",
    "nando_id": "NANDO:2200794"
  },
  {
    "id": "C0398595",
    "id2": "MedGen UID:96015",
    "medgen_label": "Myeloperoxidase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/96015",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009694",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009694",
    "nando_id": "NANDO:2200758"
  },
  {
    "id": "C0398764",
    "id2": "MedGen UID:97989",
    "medgen_label": "Recurrent Neisseria infections due to factor D deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/97989",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013487",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013487",
    "nando_id": "NANDO:2200788"
  },
  {
    "id": "C0398777",
    "id2": "MedGen UID:96024",
    "medgen_label": "Factor H deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/96024",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012350",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012350",
    "nando_id": "NANDO:2200791"
  },
  {
    "id": "C1858723",
    "id2": "MedGen UID:388129",
    "medgen_label": "Poikiloderma with neutropenia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/388129",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011405",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011405",
    "nando_id": "NANDO:2200749"
  },
  {
    "id": "C1859353",
    "id2": "MedGen UID:347128",
    "medgen_label": "Predisposition to invasive fungal disease due to CARD9 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/347128",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008905",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008905",
    "nando_id": "NANDO:2200773"
  },
  {
    "id": "C3266863",
    "id2": "MedGen UID:473805",
    "medgen_label": "Inherited susceptibility to mycobacterial diseases",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/473805",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019146",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019146",
    "nando_id": "NANDO:2200759"
  },
  {
    "id": "C3463916",
    "id2": "MedGen UID:483045",
    "medgen_label": "Factor I deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/483045",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012594",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012594",
    "nando_id": "NANDO:2200790"
  },
  {
    "id": "C3542922",
    "id2": "MedGen UID:762276",
    "medgen_label": "Immunodeficiency, common variable, 7",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/762276",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013862",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013862",
    "nando_id": "NANDO:2200801"
  },
  {
    "id": "C3552634",
    "id2": "MedGen UID:765548",
    "medgen_label": "Lymphoproliferative syndrome 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/765548",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013081",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013081",
    "nando_id": "NANDO:2200734"
  },
  {
    "id": "C3809950",
    "id2": "MedGen UID:816280",
    "medgen_label": "Complement factor b deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/816280",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014255",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014255",
    "nando_id": "NANDO:2200797"
  },
  {
    "id": "C4225260",
    "id2": "MedGen UID:904009",
    "medgen_label": "Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/904009",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014715",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014715",
    "nando_id": "NANDO:2200770"
  },
  {
    "id": "C0085859",
    "id2": "MedGen UID:39125",
    "medgen_label": "Polyglandular autoimmune syndrome, type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/39125",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009411",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009411",
    "nando_id": "NANDO:2200738"
  },
  {
    "id": "C0343047",
    "id2": "MedGen UID:91003",
    "medgen_label": "Complement component 5 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/91003",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012295",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012295",
    "nando_id": "NANDO:2200783"
  },
  {
    "id": "C0685889",
    "id2": "MedGen UID:151935",
    "medgen_label": "Familial isolated congenital asplenia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/151935",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010066",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010066",
    "nando_id": "NANDO:2200775"
  },
  {
    "id": "C1835829",
    "id2": "MedGen UID:372135",
    "medgen_label": "Primary immunodeficiency syndrome due to p14 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/372135",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012559",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012559",
    "nando_id": "NANDO:2200752"
  },
  {
    "id": "C1837174",
    "id2": "MedGen UID:332383",
    "medgen_label": "Familial hemophagocytic lymphohistiocytosis 3",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/332383",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012146",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012146",
    "nando_id": "NANDO:2200729"
  },
  {
    "id": "C1839454",
    "id2": "MedGen UID:333322",
    "medgen_label": "Properdin deficiency, X-linked",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/333322",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010713",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010713",
    "nando_id": "NANDO:2200789"
  },
  {
    "id": "C1842362",
    "id2": "MedGen UID:374912",
    "medgen_label": "Hermansky-Pudlak syndrome 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/374912",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011997",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011997",
    "nando_id": "NANDO:2200733"
  },
  {
    "id": "C1842763",
    "id2": "MedGen UID:375009",
    "medgen_label": "Spondyloenchondrodysplasia with immune dysregulation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/375009",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011939",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011939",
    "nando_id": "NANDO:2200744"
  },
  {
    "id": "C1843256",
    "id2": "MedGen UID:375137",
    "medgen_label": "Immunodeficiency 67",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/375137",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011888",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011888",
    "nando_id": "NANDO:2200762"
  },
  {
    "id": "C1845987",
    "id2": "MedGen UID:335314",
    "medgen_label": "X-linked severe congenital neutropenia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/335314",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010294",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010294",
    "nando_id": "NANDO:2200753"
  },
  {
    "id": "C1846006",
    "id2": "MedGen UID:375786",
    "medgen_label": "Ectodermal dysplasia and immune deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/375786",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010293",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010293",
    "nando_id": "NANDO:2200761"
  },
  {
    "id": "C4014605",
    "id2": "MedGen UID:863042",
    "medgen_label": "Polyglucosan body myopathy type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/863042",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014389",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014389",
    "nando_id": "NANDO:2200766"
  },
  {
    "id": "C0037917",
    "id2": "MedGen UID:21277",
    "medgen_label": "Spina bifida cystica",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21277",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0017069",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017069",
    "nando_id": "NANDO:2200814"
  },
  {
    "id": "C0272170",
    "id2": "MedGen UID:124418",
    "medgen_label": "Shwachman syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/124418",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009833",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009833",
    "nando_id": "NANDO:2200756"
  },
  {
    "id": "C0272187",
    "id2": "MedGen UID:124419",
    "medgen_label": "Leukocyte adhesion deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/124419",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017570",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017570",
    "nando_id": "NANDO:2200755"
  },
  {
    "id": "C0276226",
    "id2": "MedGen UID:75794",
    "medgen_label": "Herpes simplex encephalitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75794",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012521",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012521",
    "nando_id": "NANDO:2200772"
  },
  {
    "id": "C1863727",
    "id2": "MedGen UID:400366",
    "medgen_label": "Familial hemophagocytic lymphohistiocytosis 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/400366",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011337",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011337",
    "nando_id": "NANDO:2200728"
  },
  {
    "id": "C1863728",
    "id2": "MedGen UID:350245",
    "medgen_label": "Familial hemophagocytic lymphohistiocytosis 4",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/350245",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011336",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011336",
    "nando_id": "NANDO:2200730"
  },
  {
    "id": "C1864694",
    "id2": "MedGen UID:355270",
    "medgen_label": "Complement component 7 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/355270",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012412",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012412",
    "nando_id": "NANDO:2200785"
  },
  {
    "id": "C1864947",
    "id2": "MedGen UID:351256",
    "medgen_label": "Primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/351256",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012383",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012383",
    "nando_id": "NANDO:2200771"
  },
  {
    "id": "C1868679",
    "id2": "MedGen UID:357030",
    "medgen_label": "Griscelli syndrome type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/357030",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011872",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011872",
    "nando_id": "NANDO:2200732"
  },
  {
    "id": "C2751293",
    "id2": "MedGen UID:416514",
    "medgen_label": "Familial hemophagocytic lymphohistiocytosis 5",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/416514",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013135",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013135",
    "nando_id": "NANDO:2200731"
  },
  {
    "id": "C2752040",
    "id2": "MedGen UID:414167",
    "medgen_label": "Atypical hemolytic-uremic syndrome with MCP/CD46 anomaly",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/414167",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013040",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013040",
    "nando_id": "NANDO:2200803"
  },
  {
    "id": "C4303860",
    "id2": "MedGen UID:929529",
    "medgen_label": "3MC syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/929529",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017398",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017398",
    "nando_id": "NANDO:2200792"
  },
  {
    "id": "C5435698",
    "id2": "MedGen UID:1734133",
    "medgen_label": "Growth hormone insensitivity with immune dysregulation 1, autosomal recessive",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1734133",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0100211",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0100211",
    "nando_id": "NANDO:2200737"
  },
  {
    "id": "C0014522",
    "id2": "MedGen UID:41831",
    "medgen_label": "Epidermodysplasia verruciformis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/41831",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009176",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009176",
    "nando_id": "NANDO:2200768"
  },
  {
    "id": "C0018203",
    "id2": "MedGen UID:5377",
    "medgen_label": "Chronic granulomatous disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5377",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018305",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018305",
    "nando_id": "NANDO:2200757"
  },
  {
    "id": "C0019243",
    "id2": "MedGen UID:9229",
    "medgen_label": "Hereditary angioneurotic edema",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9229",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019623",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019623",
    "nando_id": "NANDO:2200795"
  },
  {
    "id": "C0574083",
    "id2": "MedGen UID:107893",
    "medgen_label": "3-Methylglutaconic aciduria type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/107893",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010543",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010543",
    "nando_id": "NANDO:2200751"
  },
  {
    "id": "C1540912",
    "id2": "MedGen UID:280990",
    "medgen_label": "Hypereosinophilic syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/280990",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0015691",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015691",
    "nando_id": "NANDO:2200805"
  },
  {
    "id": "C0001175",
    "id2": "MedGen UID:99",
    "medgen_label": "AIDS",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/99",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012268",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012268",
    "nando_id": "NANDO:2200809"
  },
  {
    "id": "C2676767",
    "id2": "MedGen UID:393582",
    "medgen_label": "Primary CD59 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/393582",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012858",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012858",
    "nando_id": "NANDO:2200804"
  },
  {
    "id": "C0025312",
    "id2": "MedGen UID:7538",
    "medgen_label": "Myelomeningocele",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7538",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019773",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019773",
    "nando_id": "NANDO:2200814"
  },
  {
    "id": "C0266456",
    "id2": "MedGen UID:82743",
    "medgen_label": "Meningoencephalocele",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82743",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017079",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017079",
    "nando_id": "NANDO:2200813"
  },
  {
    "id": "C0266463",
    "id2": "MedGen UID:78604",
    "medgen_label": "Lissencephaly",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78604",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018838",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018838",
    "nando_id": "NANDO:2200817"
  },
  {
    "id": "C0266484",
    "id2": "MedGen UID:78606",
    "medgen_label": "Schizencephaly",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78606",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010011",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010011",
    "nando_id": "NANDO:2200818"
  },
  {
    "id": "C0347446",
    "id2": "MedGen UID:91131",
    "medgen_label": "Spinal cord lipoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/91131",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001790",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001790",
    "nando_id": "NANDO:2200815"
  },
  {
    "id": "C0079541",
    "id2": "MedGen UID:38214",
    "medgen_label": "Holoprosencephaly sequence",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/38214",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016296",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016296",
    "nando_id": "NANDO:2200819"
  },
  {
    "id": "C4016741",
    "id2": "MedGen UID:865178",
    "medgen_label": "Immunodeficiency 32B",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/865178",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009194",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009194",
    "nando_id": "NANDO:2200808"
  },
  {
    "id": "C0019693",
    "id2": "MedGen UID:5583",
    "medgen_label": "Human immunodeficiency virus infection",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5583",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005109",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005109",
    "nando_id": "NANDO:2200810"
  },
  {
    "id": "C0559459",
    "id2": "MedGen UID:107852",
    "medgen_label": "Sacrococcygeal teratoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/107852",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0042727",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0042727",
    "nando_id": "NANDO:2200816"
  },
  {
    "id": "C0867389",
    "id2": "MedGen UID:167851",
    "medgen_label": "Chronic graft versus host disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/167851",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020547",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020547",
    "nando_id": "NANDO:2200812"
  },
  {
    "id": "C1540912",
    "id2": "MedGen UID:280990",
    "medgen_label": "Hypereosinophilic syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/280990",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015691",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015691",
    "nando_id": "NANDO:2200806"
  },
  {
    "id": "C5680014",
    "id2": "MedGen UID:1826142",
    "medgen_label": "Eosinophilic gastrointestinal disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1826142",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018438",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018438",
    "nando_id": "NANDO:2200807"
  },
  {
    "id": "C1850674",
    "id2": "MedGen UID:340597",
    "medgen_label": "Congenital multicore myopathy with external ophthalmoplegia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/340597",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009712",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009712",
    "nando_id": "NANDO:2200872"
  },
  {
    "id": "C1851945",
    "id2": "MedGen UID:338823",
    "medgen_label": "Early-onset generalized limb-onset dystonia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/338823",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007492",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007492",
    "nando_id": "NANDO:2200884"
  },
  {
    "id": "C0001193",
    "id2": "MedGen UID:7858",
    "medgen_label": "Acrocephalosyndactyly type I",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7858",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007041",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007041",
    "nando_id": "NANDO:2200844"
  },
  {
    "id": "C0004779",
    "id2": "MedGen UID:2554",
    "medgen_label": "Gorlin syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/2554",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007187",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007187",
    "nando_id": "NANDO:2200828"
  },
  {
    "id": "C0007959",
    "id2": "MedGen UID:2980",
    "medgen_label": "Charcot-Marie-Tooth disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/2980",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0015626",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015626",
    "nando_id": "NANDO:2200855"
  },
  {
    "id": "C0009207",
    "id2": "MedGen UID:40363",
    "medgen_label": "Cockayne syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/40363",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016006",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016006",
    "nando_id": "NANDO:2200832"
  },
  {
    "id": "C0010273",
    "id2": "MedGen UID:1162",
    "medgen_label": "Crouzon syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1162",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007405",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007405",
    "nando_id": "NANDO:2200845"
  },
  {
    "id": "C0010964",
    "id2": "MedGen UID:4150",
    "medgen_label": "Dandy-Walker syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/4150",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009072",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009072",
    "nando_id": "NANDO:2200821"
  },
  {
    "id": "C0175699",
    "id2": "MedGen UID:64221",
    "medgen_label": "Saethre-Chotzen syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/64221",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007042",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007042",
    "nando_id": "NANDO:2200848"
  },
  {
    "id": "C0206307",
    "id2": "MedGen UID:61565",
    "medgen_label": "Spongy degeneration of central nervous system",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/61565",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010079",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010079",
    "nando_id": "NANDO:2200834"
  },
  {
    "id": "C0410174",
    "id2": "MedGen UID:140820",
    "medgen_label": "Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/140820",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009678",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009678",
    "nando_id": "NANDO:2200860"
  },
  {
    "id": "C5244016",
    "id2": "MedGen UID:1826001",
    "medgen_label": "Cerebral creatine deficiency syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1826001",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000456",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000456",
    "nando_id": "NANDO:2200842"
  },
  {
    "id": "C0026847",
    "id2": "MedGen UID:7755",
    "medgen_label": "Spinal muscular atrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7755",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001516",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001516",
    "nando_id": "NANDO:2200853"
  },
  {
    "id": "C0027888",
    "id2": "MedGen UID:45066",
    "medgen_label": "Hereditary motor and sensory neuropathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/45066",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015358",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015358",
    "nando_id": "NANDO:2200855"
  },
  {
    "id": "C0270726",
    "id2": "MedGen UID:78724",
    "medgen_label": "Alexander disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78724",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008752",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008752",
    "nando_id": "NANDO:2200835"
  },
  {
    "id": "C0544862",
    "id2": "MedGen UID:154259",
    "medgen_label": "Neurocutaneous melanocytosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/154259",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009578",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009578",
    "nando_id": "NANDO:2200827"
  },
  {
    "id": "C0546264",
    "id2": "MedGen UID:108177",
    "medgen_label": "Congenital myopathy with fiber type disproportion",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/108177",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009711",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009711",
    "nando_id": "NANDO:2200868"
  },
  {
    "id": "C0917804",
    "id2": "MedGen UID:214590",
    "medgen_label": "Cerebral arteriovenous malformation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/214590",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007154",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007154",
    "nando_id": "NANDO:2200851"
  },
  {
    "id": "C1263858",
    "id2": "MedGen UID:224728",
    "medgen_label": "Merosin deficient congenital muscular dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/224728",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011925",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011925",
    "nando_id": "NANDO:2200861"
  },
  {
    "id": "C1858854",
    "id2": "MedGen UID:347006",
    "medgen_label": "Megalencephalic leukoencephalopathy with subcortical cysts",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/347006",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011391",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011391",
    "nando_id": "NANDO:2200837"
  },
  {
    "id": "C3489724",
    "id2": "MedGen UID:483677",
    "medgen_label": "Aicardi-Goutieres syndrome 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/483677",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012429",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012429",
    "nando_id": "NANDO:2200894"
  },
  {
    "id": "C3539013",
    "id2": "MedGen UID:761287",
    "medgen_label": "Aicardi-Goutieres syndrome 6",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/761287",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014007",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014007",
    "nando_id": "NANDO:2200898"
  },
  {
    "id": "C0338503",
    "id2": "MedGen UID:90926",
    "medgen_label": "Septo-optic dysplasia sequence",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/90926",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008428",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008428",
    "nando_id": "NANDO:2200820"
  },
  {
    "id": "C1334237",
    "id2": "MedGen UID:232659",
    "medgen_label": "Intracranial cavernous angioma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/232659",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002327",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002327",
    "nando_id": "NANDO:2200852"
  },
  {
    "id": "C1835916",
    "id2": "MedGen UID:324389",
    "medgen_label": "Aicardi-Goutieres syndrome 3",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/324389",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012471",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012471",
    "nando_id": "NANDO:2200895"
  },
  {
    "id": "C1845055",
    "id2": "MedGen UID:337145",
    "medgen_label": "Alpha thalassemia-X-linked intellectual disability syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/337145",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010519",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010519",
    "nando_id": "NANDO:2200839"
  },
  {
    "id": "C4551860",
    "id2": "MedGen UID:1642667",
    "medgen_label": "Ullrich congenital muscular dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1642667",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000355",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000355",
    "nando_id": "NANDO:2200862"
  },
  {
    "id": "C0033300",
    "id2": "MedGen UID:46123",
    "medgen_label": "Hutchinson-Gilford syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/46123",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008310",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008310",
    "nando_id": "NANDO:2200833"
  },
  {
    "id": "C0035372",
    "id2": "MedGen UID:48441",
    "medgen_label": "Rett syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/48441",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010726",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010726",
    "nando_id": "NANDO:2200825"
  },
  {
    "id": "C0036391",
    "id2": "MedGen UID:19892",
    "medgen_label": "Schwartz-Jampel syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/19892",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009717",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009717",
    "nando_id": "NANDO:2200876"
  },
  {
    "id": "C0038505",
    "id2": "MedGen UID:21361",
    "medgen_label": "Sturge-Weber syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21361",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008501",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008501",
    "nando_id": "NANDO:2200830"
  },
  {
    "id": "C0040560",
    "id2": "MedGen UID:52799",
    "medgen_label": "Congenital toxoplasmosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/52799",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005715",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005715",
    "nando_id": "NANDO:2200892"
  },
  {
    "id": "C0041341",
    "id2": "MedGen UID:22518",
    "medgen_label": "Tuberous sclerosis syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/22518",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001734",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001734",
    "nando_id": "NANDO:2200826"
  },
  {
    "id": "C0043119",
    "id2": "MedGen UID:12147",
    "medgen_label": "Werner syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/12147",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010196",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010196",
    "nando_id": "NANDO:2200831"
  },
  {
    "id": "C1865285",
    "id2": "MedGen UID:355421",
    "medgen_label": "Megalencephaly-capillary malformation-polymicrogyria syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/355421",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011240",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011240",
    "nando_id": "NANDO:2200823"
  },
  {
    "id": "C2749659",
    "id2": "MedGen UID:413116",
    "medgen_label": "Aicardi-Goutieres syndrome 5",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/413116",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013059",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013059",
    "nando_id": "NANDO:2200897"
  },
  {
    "id": "C2750785",
    "id2": "MedGen UID:413043",
    "medgen_label": "Congenital muscular dystrophy due to LMNA mutation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/413043",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013178",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013178",
    "nando_id": "NANDO:2200866"
  },
  {
    "id": "C0013264",
    "id2": "MedGen UID:3925",
    "medgen_label": "Duchenne muscular dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/3925",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010679",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010679",
    "nando_id": "NANDO:2200856"
  },
  {
    "id": "C0016667",
    "id2": "MedGen UID:8912",
    "medgen_label": "Fragile X syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/8912",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010383",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010383",
    "nando_id": "NANDO:2200840"
  },
  {
    "id": "C0018523",
    "id2": "MedGen UID:6708",
    "medgen_label": "Pigmentary pallidal degeneration",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6708",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009319",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009319",
    "nando_id": "NANDO:2200886"
  },
  {
    "id": "C0019562",
    "id2": "MedGen UID:42458",
    "medgen_label": "Von Hippel-Lindau syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/42458",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008667",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008667",
    "nando_id": "NANDO:2200829"
  },
  {
    "id": "C0020074",
    "id2": "MedGen UID:6915",
    "medgen_label": "Hereditary insensitivity to pain with anhidrosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6915",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009746",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009746",
    "nando_id": "NANDO:2200854"
  },
  {
    "id": "C0238288",
    "id2": "MedGen UID:65956",
    "medgen_label": "Facioscapulohumeral muscular dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/65956",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001347",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001347",
    "nando_id": "NANDO:2200859"
  },
  {
    "id": "C0751783",
    "id2": "MedGen UID:155631",
    "medgen_label": "Lafora disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155631",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009697",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009697",
    "nando_id": "NANDO:2200881"
  },
  {
    "id": "C0751785",
    "id2": "MedGen UID:155923",
    "medgen_label": "Unverricht-Lundborg syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155923",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009698",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009698",
    "nando_id": "NANDO:2200880"
  },
  {
    "id": "C0751951",
    "id2": "MedGen UID:199773",
    "medgen_label": "Central core myopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/199773",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007294",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007294",
    "nando_id": "NANDO:2200870"
  },
  {
    "id": "C0752282",
    "id2": "MedGen UID:156050",
    "medgen_label": "Congenital structural myopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/156050",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0002921",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002921",
    "nando_id": "NANDO:2200867"
  },
  {
    "id": "C0795996",
    "id2": "MedGen UID:167090",
    "medgen_label": "Infantile bilateral striatal necrosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/167090",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015518",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015518",
    "nando_id": "NANDO:2200888"
  },
  {
    "id": "C0917713",
    "id2": "MedGen UID:182959",
    "medgen_label": "Becker muscular dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/182959",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010311",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010311",
    "nando_id": "NANDO:2200865"
  },
  {
    "id": "C5679612",
    "id2": "MedGen UID:1826007",
    "medgen_label": "Joubert syndrome and related disorders",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1826007",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015369",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015369",
    "nando_id": "NANDO:2200824"
  },
  {
    "id": "CN228925",
    "id2": "MedGen UID:833284",
    "medgen_label": "Isolated craniosynostosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/833284",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015337",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015337",
    "nando_id": "NANDO:2200843"
  },
  {
    "id": "C0175709",
    "id2": "MedGen UID:104495",
    "medgen_label": "Centronuclear myopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/104495",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018947",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018947",
    "nando_id": "NANDO:2200867"
  },
  {
    "id": "C0206157",
    "id2": "MedGen UID:61528",
    "medgen_label": "Nemaline myopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/61528",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018958",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018958",
    "nando_id": "NANDO:2200869"
  },
  {
    "id": "C0410189",
    "id2": "MedGen UID:96078",
    "medgen_label": "Emery-Dreifuss muscular dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/96078",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016830",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016830",
    "nando_id": "NANDO:2200857"
  },
  {
    "id": "C0023520",
    "id2": "MedGen UID:6070",
    "medgen_label": "Leukodystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6070",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019046",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019046",
    "nando_id": "NANDO:2200836"
  },
  {
    "id": "C0026654",
    "id2": "MedGen UID:7726",
    "medgen_label": "Moyamoya disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7726",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016820",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016820",
    "nando_id": "NANDO:2200850"
  },
  {
    "id": "C0027126",
    "id2": "MedGen UID:10239",
    "medgen_label": "Myotonic dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10239",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016107",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016107",
    "nando_id": "NANDO:2200864"
  },
  {
    "id": "C0270962",
    "id2": "MedGen UID:75731",
    "medgen_label": "Multiminicore myopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75731",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018948",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018948",
    "nando_id": "NANDO:2200871"
  },
  {
    "id": "C0270970",
    "id2": "MedGen UID:543081",
    "medgen_label": "Reducing body myopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/543081",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019948",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019948",
    "nando_id": "NANDO:2200875"
  },
  {
    "id": "C0349499",
    "id2": "MedGen UID:578789",
    "medgen_label": "Fetal cytomegalovirus syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/578789",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017409",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017409",
    "nando_id": "NANDO:2200891"
  },
  {
    "id": "C0393591",
    "id2": "MedGen UID:97953",
    "medgen_label": "Aicardi Goutieres syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/97953",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018866",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018866",
    "nando_id": "NANDO:2200893"
  },
  {
    "id": "C1275078",
    "id2": "MedGen UID:226897",
    "medgen_label": "Carpenter syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/226897",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019012",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019012",
    "nando_id": "NANDO:2200847"
  },
  {
    "id": "C0338488",
    "id2": "MedGen UID:90925",
    "medgen_label": "Alternating hemiplegia of childhood",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/90925",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016241",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016241",
    "nando_id": "NANDO:2200883"
  },
  {
    "id": "C0686353",
    "id2": "MedGen UID:151940",
    "medgen_label": "Limb-girdle muscular dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/151940",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016971",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016971",
    "nando_id": "NANDO:2200858"
  },
  {
    "id": "C0035921",
    "id2": "MedGen UID:19841",
    "medgen_label": "Congenital rubella syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/19841",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017361",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017361",
    "nando_id": "NANDO:2200890"
  },
  {
    "id": "C0037769",
    "id2": "MedGen UID:11519",
    "medgen_label": "West syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/11519",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018097",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018097",
    "nando_id": "NANDO:2200878"
  },
  {
    "id": "C0276225",
    "id2": "MedGen UID:82910",
    "medgen_label": "Congenital herpes simplex virus infection",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82910",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017381",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017381",
    "nando_id": "NANDO:2200889"
  },
  {
    "id": "C0020256",
    "id2": "MedGen UID:9336",
    "medgen_label": "Congenital hydrocephalus",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9336",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016349",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016349",
    "nando_id": "NANDO:2200822"
  },
  {
    "id": "C0238111",
    "id2": "MedGen UID:116044",
    "medgen_label": "Lennox-Gastaut syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/116044",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016532",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016532",
    "nando_id": "NANDO:2200879"
  },
  {
    "id": "C0751122",
    "id2": "MedGen UID:148243",
    "medgen_label": "Severe myoclonic epilepsy in infancy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/148243",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0100135",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0100135",
    "nando_id": "NANDO:2200877"
  },
  {
    "id": "CN221588",
    "id2": "MedGen UID:808180",
    "medgen_label": "Dopa-responsive dystonia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/808180",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016812",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016812",
    "nando_id": "NANDO:2200885"
  },
  {
    "id": "C0004903",
    "id2": "MedGen UID:2562",
    "medgen_label": "Beckwith-Wiedemann syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/2562",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007534",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007534",
    "nando_id": "NANDO:2200959"
  },
  {
    "id": "C0005411",
    "id2": "MedGen UID:14117",
    "medgen_label": "Biliary atresia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/14117",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008867",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008867",
    "nando_id": "NANDO:2200930"
  },
  {
    "id": "C0008313",
    "id2": "MedGen UID:3036",
    "medgen_label": "Sclerosing cholangitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/3036",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018646",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018646",
    "nando_id": "NANDO:2200929"
  },
  {
    "id": "C0009324",
    "id2": "MedGen UID:3532",
    "medgen_label": "Ulcerative colitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/3532",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005101",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005101",
    "nando_id": "NANDO:2200920"
  },
  {
    "id": "C0009714",
    "id2": "MedGen UID:40449",
    "medgen_label": "Congenital hepatic fibrosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/40449",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018840",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018840",
    "nando_id": "NANDO:2200936"
  },
  {
    "id": "C0010314",
    "id2": "MedGen UID:41345",
    "medgen_label": "5p partial monosomy syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/41345",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007404",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007404",
    "nando_id": "NANDO:2200961"
  },
  {
    "id": "C0010346",
    "id2": "MedGen UID:3664",
    "medgen_label": "Crohn disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/3664",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005011",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005011",
    "nando_id": "NANDO:2200921"
  },
  {
    "id": "C0011989",
    "id2": "MedGen UID:4268",
    "medgen_label": "Diaphyseal dysplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/4268",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007542",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007542",
    "nando_id": "NANDO:2200970"
  },
  {
    "id": "C0162510",
    "id2": "MedGen UID:57924",
    "medgen_label": "Caroli disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/57924",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0010913",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010913",
    "nando_id": "NANDO:2200934"
  },
  {
    "id": "C0162635",
    "id2": "MedGen UID:58144",
    "medgen_label": "Angelman syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/58144",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007113",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007113",
    "nando_id": "NANDO:2200960"
  },
  {
    "id": "C0175695",
    "id2": "MedGen UID:61232",
    "medgen_label": "Sotos syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/61232",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019349",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019349",
    "nando_id": "NANDO:2200953"
  },
  {
    "id": "C0220658",
    "id2": "MedGen UID:67390",
    "medgen_label": "Pfeiffer syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/67390",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007043",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007043",
    "nando_id": "NANDO:2200976"
  },
  {
    "id": "C2609129",
    "id2": "MedGen UID:750633",
    "medgen_label": "Autoimmune pancreatitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/750633",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015175",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015175",
    "nando_id": "NANDO:2200943"
  },
  {
    "id": "C5234850",
    "id2": "MedGen UID:1714404",
    "medgen_label": "Antley-Bixler syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1714404",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008803",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008803",
    "nando_id": "NANDO:2200975"
  },
  {
    "id": "C0023890",
    "id2": "MedGen UID:7368",
    "medgen_label": "Cirrhosis of liver",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7368",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005155",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005155",
    "nando_id": "NANDO:2200937"
  },
  {
    "id": "C0024215",
    "id2": "MedGen UID:9828",
    "medgen_label": "Intestinal lymphangiectasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9828",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018178",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018178",
    "nando_id": "NANDO:2200914"
  },
  {
    "id": "C0024796",
    "id2": "MedGen UID:44287",
    "medgen_label": "Marfan syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44287",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007947",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007947",
    "nando_id": "NANDO:2200968"
  },
  {
    "id": "C0026769",
    "id2": "MedGen UID:10123",
    "medgen_label": "Multiple sclerosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10123",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005301",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005301",
    "nando_id": "NANDO:2200904"
  },
  {
    "id": "C0026896",
    "id2": "MedGen UID:7764",
    "medgen_label": "Myasthenia gravis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7764",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009688",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009688",
    "nando_id": "NANDO:2200906"
  },
  {
    "id": "C0031269",
    "id2": "MedGen UID:18404",
    "medgen_label": "Peutz-Jeghers syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/18404",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008280",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008280",
    "nando_id": "NANDO:2200917"
  },
  {
    "id": "C0268059",
    "id2": "MedGen UID:82768",
    "medgen_label": "Neonatal hemochromatosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82768",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009275",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009275",
    "nando_id": "NANDO:2200927"
  },
  {
    "id": "C0268186",
    "id2": "MedGen UID:78647",
    "medgen_label": "Congenital glucose-galactose malabsorption",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78647",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011731",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011731",
    "nando_id": "NANDO:2200909"
  },
  {
    "id": "C0268312",
    "id2": "MedGen UID:75668",
    "medgen_label": "Progressive familial intrahepatic cholestasis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75668",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015762",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015762",
    "nando_id": "NANDO:2200933"
  },
  {
    "id": "C0268416",
    "id2": "MedGen UID:82802",
    "medgen_label": "Enterokinase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82802",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009173",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009173",
    "nando_id": "NANDO:2200910"
  },
  {
    "id": "C0270972",
    "id2": "MedGen UID:78752",
    "medgen_label": "De Lange syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78752",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016033",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016033",
    "nando_id": "NANDO:2200958"
  },
  {
    "id": "C0345893",
    "id2": "MedGen UID:87518",
    "medgen_label": "Juvenile polyposis syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/87518",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017380",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017380",
    "nando_id": "NANDO:2200916"
  },
  {
    "id": "C0393819",
    "id2": "MedGen UID:98292",
    "medgen_label": "Chronic inflammatory demyelinating polyradiculoneuropathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/98292",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006702",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006702",
    "nando_id": "NANDO:2200905"
  },
  {
    "id": "C1275081",
    "id2": "MedGen UID:266149",
    "medgen_label": "Cardio-facio-cutaneous syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/266149",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015280",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015280",
    "nando_id": "NANDO:2200967"
  },
  {
    "id": "C1283620",
    "id2": "MedGen UID:220924",
    "medgen_label": "Sucrase-isomaltase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/220924",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009114",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009114",
    "nando_id": "NANDO:2200908"
  },
  {
    "id": "C3280527",
    "id2": "MedGen UID:482157",
    "medgen_label": "Pancreatic triacylglycerol lipase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/482157",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013700",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013700",
    "nando_id": "NANDO:2200912"
  },
  {
    "id": "C4083008",
    "id2": "MedGen UID:901636",
    "medgen_label": "Guillain-Barre syndrome, familial",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/901636",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0007691",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007691",
    "nando_id": "NANDO:2200905"
  },
  {
    "id": "C4275068",
    "id2": "MedGen UID:898614",
    "medgen_label": "Chronic diarrhea due to glucoamylase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/898614",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015169",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015169",
    "nando_id": "NANDO:2200911"
  },
  {
    "id": "C4707658",
    "id2": "MedGen UID:1645136",
    "medgen_label": "Acute encephalopathy with biphasic seizures and late reduced diffusion",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1645136",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018198",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018198",
    "nando_id": "NANDO:2200901"
  },
  {
    "id": "C4721555",
    "id2": "MedGen UID:1666753",
    "medgen_label": "Autoimmune hepatitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1666753",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016264",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016264",
    "nando_id": "NANDO:2200928"
  },
  {
    "id": "C0085280",
    "id2": "MedGen UID:39014",
    "medgen_label": "Arteriohepatic dysplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/39014",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007318",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007318",
    "nando_id": "NANDO:2200931"
  },
  {
    "id": "C0152095",
    "id2": "MedGen UID:56261",
    "medgen_label": "Complete trisomy 13 syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/56261",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018068",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018068",
    "nando_id": "NANDO:2200964"
  },
  {
    "id": "C0152164",
    "id2": "MedGen UID:57509",
    "medgen_label": "Cyclical vomiting syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/57509",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010778",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010778",
    "nando_id": "NANDO:2200919"
  },
  {
    "id": "C0341305",
    "id2": "MedGen UID:83322",
    "medgen_label": "Autoimmune enteropathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/83322",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019787",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019787",
    "nando_id": "NANDO:2200923"
  },
  {
    "id": "C0341306",
    "id2": "MedGen UID:137954",
    "medgen_label": "Congenital microvillous atrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/137954",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009635",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009635",
    "nando_id": "NANDO:2200913"
  },
  {
    "id": "C0342288",
    "id2": "MedGen UID:83339",
    "medgen_label": "Insulin-dependent diabetes mellitus secretory diarrhea syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/83339",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010580",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010580",
    "nando_id": "NANDO:2200924"
  },
  {
    "id": "C0345217",
    "id2": "MedGen UID:83377",
    "medgen_label": "Cloacal exstrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/83377",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009774",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009774",
    "nando_id": "NANDO:2200951"
  },
  {
    "id": "C0345217",
    "id2": "MedGen UID:83377",
    "medgen_label": "Cloacal exstrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/83377",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009774",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009774",
    "nando_id": "NANDO:2200950"
  },
  {
    "id": "C0345240",
    "id2": "MedGen UID:83378",
    "medgen_label": "Aganglionosis, total intestinal",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/83378",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0008738",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008738",
    "nando_id": "NANDO:2200948"
  },
  {
    "id": "C0587248",
    "id2": "MedGen UID:108454",
    "medgen_label": "Costello syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/108454",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009026",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009026",
    "nando_id": "NANDO:2200971"
  },
  {
    "id": "C5551003",
    "id2": "MedGen UID:1789261",
    "medgen_label": "Crigler-Najjar syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1789261",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009044",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009044",
    "nando_id": "NANDO:2200941"
  },
  {
    "id": "C5568838",
    "id2": "MedGen UID:1800261",
    "medgen_label": "Chronic enteropathy associated with SLCO2A1 gene",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1800261",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018766",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018766",
    "nando_id": "NANDO:2200925"
  },
  {
    "id": "C5671289",
    "id2": "MedGen UID:1804547",
    "medgen_label": "Autoimmune encephalitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1804547",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020640",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020640",
    "nando_id": "NANDO:2200902"
  },
  {
    "id": "C0032580",
    "id2": "MedGen UID:46010",
    "medgen_label": "Familial multiple polyposis syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/46010",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0021055",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0021055",
    "nando_id": "NANDO:2200915"
  },
  {
    "id": "C0035934",
    "id2": "MedGen UID:48517",
    "medgen_label": "Rubinstein-Taybi syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/48517",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019188",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019188",
    "nando_id": "NANDO:2200955"
  },
  {
    "id": "C0036992",
    "id2": "MedGen UID:19966",
    "medgen_label": "Short bowel syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/19966",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015183",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015183",
    "nando_id": "NANDO:2200944"
  },
  {
    "id": "C0038522",
    "id2": "MedGen UID:52527",
    "medgen_label": "Subacute sclerosing panencephalitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/52527",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009835",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009835",
    "nando_id": "NANDO:2200899"
  },
  {
    "id": "C1956097",
    "id2": "MedGen UID:408255",
    "medgen_label": "4p partial monosomy syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/408255",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008684",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008684",
    "nando_id": "NANDO:2200962"
  },
  {
    "id": "C2697932",
    "id2": "MedGen UID:395827",
    "medgen_label": "Loeys-Dietz syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/395827",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018954",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018954",
    "nando_id": "NANDO:2200969"
  },
  {
    "id": "C2930868",
    "id2": "MedGen UID:418934",
    "medgen_label": "Rasmussen subacute encephalitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/418934",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016019",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016019",
    "nando_id": "NANDO:2200900"
  },
  {
    "id": "C4317091",
    "id2": "MedGen UID:1384417",
    "medgen_label": "Trisomy 18",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1384417",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018071",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018071",
    "nando_id": "NANDO:2200963"
  },
  {
    "id": "C0013080",
    "id2": "MedGen UID:4385",
    "medgen_label": "Down syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/4385",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008608",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008608",
    "nando_id": "NANDO:2200965"
  },
  {
    "id": "C0018522",
    "id2": "MedGen UID:5414",
    "medgen_label": "Hallermann-Streiff syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5414",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009318",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009318",
    "nando_id": "NANDO:2200973"
  },
  {
    "id": "C0018553",
    "id2": "MedGen UID:5420",
    "medgen_label": "Cowden syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5420",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016063",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016063",
    "nando_id": "NANDO:2200918"
  },
  {
    "id": "C0019569",
    "id2": "MedGen UID:5559",
    "medgen_label": "Aganglionic megacolon",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5559",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018309",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018309",
    "nando_id": "NANDO:2200948"
  },
  {
    "id": "C0019569",
    "id2": "MedGen UID:5559",
    "medgen_label": "Aganglionic megacolon",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5559",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018309",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018309",
    "nando_id": "NANDO:2200945"
  },
  {
    "id": "C0020541",
    "id2": "MedGen UID:9375",
    "medgen_label": "Portal hypertension",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9375",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005080",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005080",
    "nando_id": "NANDO:2200938"
  },
  {
    "id": "C0021171",
    "id2": "MedGen UID:7049",
    "medgen_label": "Incontinentia pigmenti syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7049",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010631",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010631",
    "nando_id": "NANDO:2200974"
  },
  {
    "id": "C0021345",
    "id2": "MedGen UID:7069",
    "medgen_label": "Infectious mononucleosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7069",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0005810",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005810",
    "nando_id": "NANDO:2200976"
  },
  {
    "id": "C0238062",
    "id2": "MedGen UID:536759",
    "medgen_label": "Chronic intestinal pseudoobstruction",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/536759",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017574",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017574",
    "nando_id": "NANDO:2200946"
  },
  {
    "id": "C0238339",
    "id2": "MedGen UID:116056",
    "medgen_label": "Hereditary pancreatitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/116056",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008185",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008185",
    "nando_id": "NANDO:2200942"
  },
  {
    "id": "C0265210",
    "id2": "MedGen UID:120511",
    "medgen_label": "Weaver syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120511",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010193",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010193",
    "nando_id": "NANDO:2200957"
  },
  {
    "id": "C0265252",
    "id2": "MedGen UID:75556",
    "medgen_label": "Coffin-Lowry syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75556",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010561",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010561",
    "nando_id": "NANDO:2200952"
  },
  {
    "id": "C0265338",
    "id2": "MedGen UID:75565",
    "medgen_label": "Coffin-Siris syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75565",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015452",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015452",
    "nando_id": "NANDO:2200977"
  },
  {
    "id": "C0265354",
    "id2": "MedGen UID:75567",
    "medgen_label": "CHARGE syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75567",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008965",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008965",
    "nando_id": "NANDO:2200972"
  },
  {
    "id": "C0566602",
    "id2": "MedGen UID:107565",
    "medgen_label": "Primary sclerosing cholangitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/107565",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013433",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013433",
    "nando_id": "NANDO:2200929"
  },
  {
    "id": "C0795864",
    "id2": "MedGen UID:162881",
    "medgen_label": "Smith-Magenis syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/162881",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008434",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008434",
    "nando_id": "NANDO:2200954"
  },
  {
    "id": "C0796004",
    "id2": "MedGen UID:162897",
    "medgen_label": "Kabuki syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/162897",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016512",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016512",
    "nando_id": "NANDO:2200956"
  },
  {
    "id": "C4049262",
    "id2": "MedGen UID:1381987",
    "medgen_label": "Febrile infection-related epilepsy syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1381987",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015584",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015584",
    "nando_id": "NANDO:2200903"
  },
  {
    "id": "C5700203",
    "id2": "MedGen UID:1814547",
    "medgen_label": "Caroli syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1814547",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018808",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018808",
    "nando_id": "NANDO:2200934"
  },
  {
    "id": "C1846058",
    "id2": "MedGen UID:337496",
    "medgen_label": "Syndromic X-linked intellectual disability Lubs type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/337496",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010283",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010283",
    "nando_id": "NANDO:2200984"
  },
  {
    "id": "C0007194",
    "id2": "MedGen UID:2881",
    "medgen_label": "Hypertrophic cardiomyopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/2881",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0005045",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005045",
    "nando_id": "NANDO:2201042"
  },
  {
    "id": "C0162678",
    "id2": "MedGen UID:58149",
    "medgen_label": "Neurofibromatosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/58149",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0021061",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0021061",
    "nando_id": "NANDO:2201003"
  },
  {
    "id": "C0175694",
    "id2": "MedGen UID:61231",
    "medgen_label": "Smith-Lemli-Opitz syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/61231",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010035",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010035",
    "nando_id": "NANDO:2200979"
  },
  {
    "id": "C0221060",
    "id2": "MedGen UID:66357",
    "medgen_label": "Oromandibular-limb hypogenesis spectrum",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/66357",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008006",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008006",
    "nando_id": "NANDO:2200980"
  },
  {
    "id": "C0027122",
    "id2": "MedGen UID:6503",
    "medgen_label": "Myositis ossificans",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6503",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0003964",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003964",
    "nando_id": "NANDO:2201020"
  },
  {
    "id": "C1856113",
    "id2": "MedGen UID:341067",
    "medgen_label": "Mowat-Wilson syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/341067",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009341",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009341",
    "nando_id": "NANDO:2200981"
  },
  {
    "id": "C1863557",
    "id2": "MedGen UID:350209",
    "medgen_label": "Blepharophimosis - intellectual disability syndrome, SBBYS type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/350209",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011365",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011365",
    "nando_id": "NANDO:2200982"
  },
  {
    "id": "C4225222",
    "id2": "MedGen UID:906646",
    "medgen_label": "Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/906646",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014757",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014757",
    "nando_id": "NANDO:2200985"
  },
  {
    "id": "C4225671",
    "id2": "MedGen UID:902479",
    "medgen_label": "VATER association",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/902479",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008642",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008642",
    "nando_id": "NANDO:2200983"
  },
  {
    "id": "C4707798",
    "id2": "MedGen UID:1647610",
    "medgen_label": "Multiple epiphyseal dysplasia due to collagen 9 anomaly",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1647610",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0015627",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015627",
    "nando_id": "NANDO:2201016"
  },
  {
    "id": "C0078918",
    "id2": "MedGen UID:36250",
    "medgen_label": "Oculocutaneous albinism",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/36250",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018910",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018910",
    "nando_id": "NANDO:2200986"
  },
  {
    "id": "C4317043",
    "id2": "MedGen UID:1387611",
    "medgen_label": "Simpson-Golabi-Behmel syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1387611",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010731",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010731",
    "nando_id": "NANDO:2200978"
  },
  {
    "id": "C4511307",
    "id2": "MedGen UID:1393111",
    "medgen_label": "Keratinopathic ichthyosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1393111",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017266",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017266",
    "nando_id": "NANDO:2200987"
  },
  {
    "id": "C5437635",
    "id2": "MedGen UID:1725198",
    "medgen_label": "Autosomal recessive epidermolytic ichthyosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1725198",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0044742",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0044742",
    "nando_id": "NANDO:2200989"
  },
  {
    "id": "C0015306",
    "id2": "MedGen UID:4612",
    "medgen_label": "Multiple congenital exostosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/4612",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0005508",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005508",
    "nando_id": "NANDO:2201014"
  },
  {
    "id": "C0265282",
    "id2": "MedGen UID:82700",
    "medgen_label": "Fibrochondrogenesis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82700",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0016068",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016068",
    "nando_id": "NANDO:2201016"
  },
  {
    "id": "CN293953",
    "id2": "MedGen UID:978511",
    "medgen_label": "Neutral lipid storage disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/978511",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0015611",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015611",
    "nando_id": "NANDO:2200997"
  },
  {
    "id": "CN377632",
    "id2": "MedGen UID:1052865",
    "medgen_label": "Autosomal dominant epidermolytic ichthyosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1052865",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020702",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020702",
    "nando_id": "NANDO:2200988"
  },
  {
    "id": "C0001080",
    "id2": "MedGen UID:1289",
    "medgen_label": "Achondroplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1289",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007037",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007037",
    "nando_id": "NANDO:2201009"
  },
  {
    "id": "C0003872",
    "id2": "MedGen UID:2077",
    "medgen_label": "Psoriatic arthritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/2077",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011849",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011849",
    "nando_id": "NANDO:2201059"
  },
  {
    "id": "C0008445",
    "id2": "MedGen UID:3052",
    "medgen_label": "Chondrodysplasia punctata",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/3052",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019701",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019701",
    "nando_id": "NANDO:2201017"
  },
  {
    "id": "C0175778",
    "id2": "MedGen UID:104500",
    "medgen_label": "Larsen syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/104500",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007875",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007875",
    "nando_id": "NANDO:2201019"
  },
  {
    "id": "C0220668",
    "id2": "MedGen UID:67391",
    "medgen_label": "Congenital contractural arachnodactyly",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/67391",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007363",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007363",
    "nando_id": "NANDO:2201026"
  },
  {
    "id": "C0221025",
    "id2": "MedGen UID:65122",
    "medgen_label": "Kasabach-Merritt syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/65122",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007708",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007708",
    "nando_id": "NANDO:2201035"
  },
  {
    "id": "C0409818",
    "id2": "MedGen UID:98370",
    "medgen_label": "Chronic infantile neurological, cutaneous and articular syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/98370",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011776",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011776",
    "nando_id": "NANDO:2201066"
  },
  {
    "id": "C0410529",
    "id2": "MedGen UID:98376",
    "medgen_label": "Hypochondroplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/98376",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007793",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007793",
    "nando_id": "NANDO:2201010"
  },
  {
    "id": "C0410538",
    "id2": "MedGen UID:98378",
    "medgen_label": "Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/98378",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008322",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008322",
    "nando_id": "NANDO:2201018"
  },
  {
    "id": "C2931825",
    "id2": "MedGen UID:444150",
    "medgen_label": "Negative rheumatoid factor polyarthritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/444150",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0043152",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0043152",
    "nando_id": "NANDO:2201057"
  },
  {
    "id": "C5848103",
    "id2": "MedGen UID:1853123",
    "medgen_label": "Hypohidrotic ectodermal dysplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1853123",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016535",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016535",
    "nando_id": "NANDO:2201005"
  },
  {
    "id": "C0022739",
    "id2": "MedGen UID:9646",
    "medgen_label": "Angioosteohypertrophic syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9646",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007864",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007864",
    "nando_id": "NANDO:2201030"
  },
  {
    "id": "C0024221",
    "id2": "MedGen UID:6153",
    "medgen_label": "Lymphangioma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6153",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002013",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002013",
    "nando_id": "NANDO:2201032"
  },
  {
    "id": "C0025268",
    "id2": "MedGen UID:9958",
    "medgen_label": "Multiple endocrine neoplasia type 2A",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9958",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008234",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008234",
    "nando_id": "NANDO:2201052"
  },
  {
    "id": "C0025269",
    "id2": "MedGen UID:9959",
    "medgen_label": "Multiple endocrine neoplasia type 2B",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9959",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008082",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008082",
    "nando_id": "NANDO:2201053"
  },
  {
    "id": "C0027831",
    "id2": "MedGen UID:18013",
    "medgen_label": "Neurofibromatosis, type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/18013",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018975",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018975",
    "nando_id": "NANDO:2201003"
  },
  {
    "id": "C0029411",
    "id2": "MedGen UID:18210",
    "medgen_label": "Pachydermoperiostosis syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/18210",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016620",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016620",
    "nando_id": "NANDO:2201004"
  },
  {
    "id": "C0029434",
    "id2": "MedGen UID:45246",
    "medgen_label": "Osteogenesis imperfecta",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/45246",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019019",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019019",
    "nando_id": "NANDO:2201011"
  },
  {
    "id": "C0029454",
    "id2": "MedGen UID:18223",
    "medgen_label": "Osteopetrosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/18223",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017198",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017198",
    "nando_id": "NANDO:2201013"
  },
  {
    "id": "C0029455",
    "id2": "MedGen UID:45251",
    "medgen_label": "Osteopoikilosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/45251",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001414",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001414",
    "nando_id": "NANDO:2201024"
  },
  {
    "id": "C0029464",
    "id2": "MedGen UID:10502",
    "medgen_label": "Increased bone mineral density",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10502",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002933",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002933",
    "nando_id": "NANDO:2201022"
  },
  {
    "id": "C0268238",
    "id2": "MedGen UID:82780",
    "medgen_label": "Triglyceride storage disease with ichthyosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82780",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010155",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010155",
    "nando_id": "NANDO:2200997"
  },
  {
    "id": "C0346072",
    "id2": "MedGen UID:83401",
    "medgen_label": "Blue rubber bleb nevus",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/83401",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007203",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007203",
    "nando_id": "NANDO:2201027"
  },
  {
    "id": "C0432306",
    "id2": "MedGen UID:98153",
    "medgen_label": "Ichthyosis bullosa of Siemens",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/98153",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007813",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007813",
    "nando_id": "NANDO:2200990"
  },
  {
    "id": "C1274215",
    "id2": "MedGen UID:697564",
    "medgen_label": "Autosomal recessive congenital ichthyosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/697564",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017265",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017265",
    "nando_id": "NANDO:2200991"
  },
  {
    "id": "C1858558",
    "id2": "MedGen UID:346934",
    "medgen_label": "Systemic-onset juvenile idiopathic arthritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/346934",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019434",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019434",
    "nando_id": "NANDO:2201055"
  },
  {
    "id": "C3495919",
    "id2": "MedGen UID:854059",
    "medgen_label": "Enthesitis-related juvenile idiopathic arthritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/854059",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019437",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019437",
    "nando_id": "NANDO:2201060"
  },
  {
    "id": "C3665333",
    "id2": "MedGen UID:777082",
    "medgen_label": "Keratitis ichthyosis and deafness syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/777082",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018781",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018781",
    "nando_id": "NANDO:2200996"
  },
  {
    "id": "C0152081",
    "id2": "MedGen UID:508876",
    "medgen_label": "Pustular psoriasis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/508876",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0022205",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0022205",
    "nando_id": "NANDO:2201001"
  },
  {
    "id": "C0340231",
    "id2": "MedGen UID:137939",
    "medgen_label": "Tracheobronchomalacia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/137939",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008888",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008888",
    "nando_id": "NANDO:2201040"
  },
  {
    "id": "C0340543",
    "id2": "MedGen UID:90953",
    "medgen_label": "Heritable pulmonary arterial hypertension",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/90953",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017148",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017148",
    "nando_id": "NANDO:2201047"
  },
  {
    "id": "C0342394",
    "id2": "MedGen UID:574999",
    "medgen_label": "Neurohypophyseal diabetes insipidus",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/574999",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007450",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007450",
    "nando_id": "NANDO:2201050"
  },
  {
    "id": "C0598226",
    "id2": "MedGen UID:108615",
    "medgen_label": "Autosomal recessive congenital ichthyosis 4B",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/108615",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009443",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009443",
    "nando_id": "NANDO:2200992"
  },
  {
    "id": "C3839921",
    "id2": "MedGen UID:825766",
    "medgen_label": "Diffuse lymphatic malformation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/825766",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015408",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015408",
    "nando_id": "NANDO:2201033"
  },
  {
    "id": "C3890733",
    "id2": "MedGen UID:855737",
    "medgen_label": "Rheumatoid factor-positive polyarticular juvenile idiopathic arthritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/855737",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019435",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019435",
    "nando_id": "NANDO:2201058"
  },
  {
    "id": "C5574950",
    "id2": "MedGen UID:1802991",
    "medgen_label": "Netherton syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1802991",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009735",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009735",
    "nando_id": "NANDO:2200993"
  },
  {
    "id": "C5576443",
    "id2": "MedGen UID:1804666",
    "medgen_label": "Primary lymphedema",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1804666",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019175",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019175",
    "nando_id": "NANDO:2201031"
  },
  {
    "id": "C0037231",
    "id2": "MedGen UID:11443",
    "medgen_label": "Sjögren-Larsson syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/11443",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010031",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010031",
    "nando_id": "NANDO:2200994"
  },
  {
    "id": "C0038325",
    "id2": "MedGen UID:20955",
    "medgen_label": "Stevens-Johnson syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/20955",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018229",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018229",
    "nando_id": "NANDO:2201006"
  },
  {
    "id": "C0039445",
    "id2": "MedGen UID:52657",
    "medgen_label": "Hereditary hemorrhagic telangiectasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/52657",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019180",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019180",
    "nando_id": "NANDO:2201034"
  },
  {
    "id": "C0043346",
    "id2": "MedGen UID:21943",
    "medgen_label": "Xeroderma pigmentosum",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21943",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019600",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019600",
    "nando_id": "NANDO:2201002"
  },
  {
    "id": "C2931073",
    "id2": "MedGen UID:419326",
    "medgen_label": "Type 2 collagenopathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/419326",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0022800",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0022800",
    "nando_id": "NANDO:2201016"
  },
  {
    "id": "C2931171",
    "id2": "MedGen UID:443993",
    "medgen_label": "Oligoarticular juvenile idiopathic arthritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/443993",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019433",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019433",
    "nando_id": "NANDO:2201056"
  },
  {
    "id": "C5399971",
    "id2": "MedGen UID:1746744",
    "medgen_label": "IFAP syndrome 1, with or without BRESHECK syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1746744",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0100213",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0100213",
    "nando_id": "NANDO:2200999"
  },
  {
    "id": "C0014084",
    "id2": "MedGen UID:41775",
    "medgen_label": "Enchondromatosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/41775",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008145",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008145",
    "nando_id": "NANDO:2201015"
  },
  {
    "id": "C0014518",
    "id2": "MedGen UID:4501",
    "medgen_label": "Toxic epidermal necrolysis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/4501",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019810",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019810",
    "nando_id": "NANDO:2201007"
  },
  {
    "id": "C0014527",
    "id2": "MedGen UID:41832",
    "medgen_label": "Epidermolysis bullosa",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/41832",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006541",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006541",
    "nando_id": "NANDO:2201000"
  },
  {
    "id": "C0015306",
    "id2": "MedGen UID:4612",
    "medgen_label": "Multiple congenital exostosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/4612",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005508",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005508",
    "nando_id": "NANDO:2201015"
  },
  {
    "id": "C0016037",
    "id2": "MedGen UID:4698",
    "medgen_label": "Progressive myositis ossificans",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/4698",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007606",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007606",
    "nando_id": "NANDO:2201020"
  },
  {
    "id": "C0020630",
    "id2": "MedGen UID:43799",
    "medgen_label": "Hypophosphatasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/43799",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018570",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018570",
    "nando_id": "NANDO:2201012"
  },
  {
    "id": "C0238402",
    "id2": "MedGen UID:116061",
    "medgen_label": "Pyknodysostosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/116061",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009940",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009940",
    "nando_id": "NANDO:2201023"
  },
  {
    "id": "C0238462",
    "id2": "MedGen UID:66772",
    "medgen_label": "Medullary thyroid carcinoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/66772",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015277",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015277",
    "nando_id": "NANDO:2201054"
  },
  {
    "id": "C0265267",
    "id2": "MedGen UID:82697",
    "medgen_label": "Child syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82697",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010621",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010621",
    "nando_id": "NANDO:2200998"
  },
  {
    "id": "C0854914",
    "id2": "MedGen UID:163163",
    "medgen_label": "bilateral retinoblastoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/163163",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0003075",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003075",
    "nando_id": "NANDO:2201038"
  },
  {
    "id": "C5680196",
    "id2": "MedGen UID:1842681",
    "medgen_label": "Unspecified juvenile idiopathic arthritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1842681",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019607",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019607",
    "nando_id": "NANDO:2201061"
  },
  {
    "id": "C5680597",
    "id2": "MedGen UID:1842414",
    "medgen_label": "Thoracic malformation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1842414",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015929",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015929",
    "nando_id": "NANDO:2201008"
  },
  {
    "id": "C5680977",
    "id2": "MedGen UID:1842686",
    "medgen_label": "TRPV4-related bone disorder",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1842686",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018240",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018240",
    "nando_id": "NANDO:2201021"
  },
  {
    "id": "C1833382",
    "id2": "MedGen UID:318863",
    "medgen_label": "Maturity-onset diabetes of the young type 4",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/318863",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011667",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011667",
    "nando_id": "NANDO:2201072"
  },
  {
    "id": "C1833518",
    "id2": "MedGen UID:318896",
    "medgen_label": "Carnitine palmitoyl transferase II deficiency, neonatal form",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/318896",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012136",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012136",
    "nando_id": "NANDO:2201132"
  },
  {
    "id": "C1848552",
    "id2": "MedGen UID:341253",
    "medgen_label": "Methylmalonic aciduria and homocystinuria type cblD",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/341253",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010185",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010185",
    "nando_id": "NANDO:2201108"
  },
  {
    "id": "C1848561",
    "id2": "MedGen UID:341256",
    "medgen_label": "Cobalamin C disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/341256",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010184",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010184",
    "nando_id": "NANDO:2201107"
  },
  {
    "id": "C1848578",
    "id2": "MedGen UID:336373",
    "medgen_label": "Methylmalonic aciduria and homocystinuria type cblF",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/336373",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010183",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010183",
    "nando_id": "NANDO:2201110"
  },
  {
    "id": "C1849722",
    "id2": "MedGen UID:342338",
    "medgen_label": "Adult polyglucosan body disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/342338",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009897",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009897",
    "nando_id": "NANDO:2201163"
  },
  {
    "id": "C1852093",
    "id2": "MedGen UID:377589",
    "medgen_label": "Maturity-onset diabetes of the young type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/377589",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007452",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007452",
    "nando_id": "NANDO:2201069"
  },
  {
    "id": "C1855102",
    "id2": "MedGen UID:344420",
    "medgen_label": "Methylmalonic aciduria, cblB type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/344420",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009614",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009614",
    "nando_id": "NANDO:2201106"
  },
  {
    "id": "C1855109",
    "id2": "MedGen UID:344422",
    "medgen_label": "Methylmalonic aciduria, cblA type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/344422",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009613",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009613",
    "nando_id": "NANDO:2201105"
  },
  {
    "id": "C1855128",
    "id2": "MedGen UID:344426",
    "medgen_label": "Methylcobalamin deficiency type cblG",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/344426",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009609",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009609",
    "nando_id": "NANDO:2201111"
  },
  {
    "id": "C0023786",
    "id2": "MedGen UID:44171",
    "medgen_label": "Mucopolysaccharidosis type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44171",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0001586",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001586",
    "nando_id": "NANDO:2201168"
  },
  {
    "id": "C0026708",
    "id2": "MedGen UID:6453",
    "medgen_label": "Mucopolysaccharidosis, MPS-I-S",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/6453",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011760",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011760",
    "nando_id": "NANDO:2201169"
  },
  {
    "id": "C0031485",
    "id2": "MedGen UID:19244",
    "medgen_label": "Phenylketonuria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/19244",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009861",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009861",
    "nando_id": "NANDO:2201075"
  },
  {
    "id": "C0268146",
    "id2": "MedGen UID:78644",
    "medgen_label": "Glucose-6-phosphate transport defect",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78644",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009288",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009288",
    "nando_id": "NANDO:2201154"
  },
  {
    "id": "C0268390",
    "id2": "MedGen UID:120634",
    "medgen_label": "Familial amyloid nephropathy with urticaria AND deafness",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120634",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008633",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008633",
    "nando_id": "NANDO:2201067"
  },
  {
    "id": "C0268543",
    "id2": "MedGen UID:120649",
    "medgen_label": "Hyperammonemia, type III",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120649",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009377",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009377",
    "nando_id": "NANDO:2201084"
  },
  {
    "id": "C0268601",
    "id2": "MedGen UID:78692",
    "medgen_label": "Deficiency of hydroxymethylglutaryl-CoA lyase",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78692",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009520",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009520",
    "nando_id": "NANDO:2201119"
  },
  {
    "id": "C0431693",
    "id2": "MedGen UID:96569",
    "medgen_label": "Renal cysts and diabetes syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/96569",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007669",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007669",
    "nando_id": "NANDO:2201073"
  },
  {
    "id": "C0543514",
    "id2": "MedGen UID:107772",
    "medgen_label": "Glycogen storage disease IXb",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/107772",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009868",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009868",
    "nando_id": "NANDO:2201165"
  },
  {
    "id": "C1855861",
    "id2": "MedGen UID:343430",
    "medgen_label": "Glycogen storage disorder due to hepatic glycogen synthase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/343430",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009414",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009414",
    "nando_id": "NANDO:2201151"
  },
  {
    "id": "C1856057",
    "id2": "MedGen UID:344640",
    "medgen_label": "Methylcobalamin deficiency type cblE",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/344640",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009354",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009354",
    "nando_id": "NANDO:2201109"
  },
  {
    "id": "C3694531",
    "id2": "MedGen UID:854172",
    "medgen_label": "Glycogen storage disease IXa1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/854172",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010598",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010598",
    "nando_id": "NANDO:2201164"
  },
  {
    "id": "C0086431",
    "id2": "MedGen UID:88566",
    "medgen_label": "Mucopolysaccharidosis, MPS-I-H/S",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/88566",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011759",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011759",
    "nando_id": "NANDO:2201170"
  },
  {
    "id": "C0086647",
    "id2": "MedGen UID:39264",
    "medgen_label": "Mucopolysaccharidosis, MPS-III-A",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/39264",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009655",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009655",
    "nando_id": "NANDO:2201174"
  },
  {
    "id": "C0086648",
    "id2": "MedGen UID:88601",
    "medgen_label": "Mucopolysaccharidosis, MPS-III-B",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/88601",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009656",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009656",
    "nando_id": "NANDO:2201175"
  },
  {
    "id": "C0086795",
    "id2": "MedGen UID:39698",
    "medgen_label": "Hurler syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/39698",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0011758",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011758",
    "nando_id": "NANDO:2201168"
  },
  {
    "id": "C0342277",
    "id2": "MedGen UID:87434",
    "medgen_label": "Maturity-onset diabetes of the young type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/87434",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007453",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007453",
    "nando_id": "NANDO:2201070"
  },
  {
    "id": "C0342790",
    "id2": "MedGen UID:137978",
    "medgen_label": "Carnitine palmitoyltransferase II deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/137978",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0015515",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015515",
    "nando_id": "NANDO:2201133"
  },
  {
    "id": "C0342790",
    "id2": "MedGen UID:137978",
    "medgen_label": "Carnitine palmitoyltransferase II deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/137978",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0015515",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015515",
    "nando_id": "NANDO:2201134"
  },
  {
    "id": "C0342841",
    "id2": "MedGen UID:575246",
    "medgen_label": "Mucopolysaccharidosis type 2, severe form",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/575246",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016315",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016315",
    "nando_id": "NANDO:2201173"
  },
  {
    "id": "C1838100",
    "id2": "MedGen UID:324942",
    "medgen_label": "Maturity-onset diabetes of the young type 3",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/324942",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010894",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010894",
    "nando_id": "NANDO:2201071"
  },
  {
    "id": "C1845151",
    "id2": "MedGen UID:335112",
    "medgen_label": "Glycogen storage disease IXd",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/335112",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010362",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010362",
    "nando_id": "NANDO:2201167"
  },
  {
    "id": "C3887523",
    "id2": "MedGen UID:854382",
    "medgen_label": "Very long chain acyl-CoA dehydrogenase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/854382",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0008723",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008723",
    "nando_id": "NANDO:2201139"
  },
  {
    "id": "C1969054",
    "id2": "MedGen UID:409741",
    "medgen_label": "Glycogen storage disease due to muscle and heart glycogen synthase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/409741",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012693",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012693",
    "nando_id": "NANDO:2201152"
  },
  {
    "id": "C1969443",
    "id2": "MedGen UID:370665",
    "medgen_label": "Mitochondrial trifunctional protein deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/370665",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0012172",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012172",
    "nando_id": "NANDO:2201147"
  },
  {
    "id": "C2751643",
    "id2": "MedGen UID:442778",
    "medgen_label": "Glycogen storage disease IXc",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/442778",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013091",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013091",
    "nando_id": "NANDO:2201166"
  },
  {
    "id": "C2919796",
    "id2": "MedGen UID:415885",
    "medgen_label": "Glycogen storage disease due to glucose-6-phosphatase deficiency type IA",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/415885",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009287",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009287",
    "nando_id": "NANDO:2201153"
  },
  {
    "id": "C5679815",
    "id2": "MedGen UID:1826165",
    "medgen_label": "Mucopolysaccharidosis type 2, attenuated form",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1826165",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0016316",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016316",
    "nando_id": "NANDO:2201172"
  },
  {
    "id": "C1621920",
    "id2": "MedGen UID:301223",
    "medgen_label": "Intermediate maple syrup urine disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/301223",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017052",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017052",
    "nando_id": "NANDO:2201079"
  },
  {
    "id": "C0268568",
    "id2": "MedGen UID:78689",
    "medgen_label": "Classical maple syrup urine disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78689",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017051",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017051",
    "nando_id": "NANDO:2201078"
  },
  {
    "id": "C0268569",
    "id2": "MedGen UID:78690",
    "medgen_label": "Intermittent maple syrup urine disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78690",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017053",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017053",
    "nando_id": "NANDO:2201080"
  },
  {
    "id": "C0268611",
    "id2": "MedGen UID:75697",
    "medgen_label": "Arakawa syndrome 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75697",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0021915",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0021915",
    "nando_id": "NANDO:2201111"
  },
  {
    "id": "C1856302",
    "id2": "MedGen UID:344701",
    "medgen_label": "Glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/344701",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017696",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017696",
    "nando_id": "NANDO:2201160"
  },
  {
    "id": "C1856303",
    "id2": "MedGen UID:383883",
    "medgen_label": "Glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/383883",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017697",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017697",
    "nando_id": "NANDO:2201161"
  },
  {
    "id": "C0343068",
    "id2": "MedGen UID:137986",
    "medgen_label": "Familial cold autoinflammatory syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/137986",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018768",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018768",
    "nando_id": "NANDO:2201068"
  },
  {
    "id": "C0751285",
    "id2": "MedGen UID:199627",
    "medgen_label": "Thiamine-responsive maple syrup urine disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/199627",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017054",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017054",
    "nando_id": "NANDO:2201081"
  },
  {
    "id": "C5679618",
    "id2": "MedGen UID:1843387",
    "medgen_label": "Acute neonatal citrullinemia type I",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1843387",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016600",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016600",
    "nando_id": "NANDO:2201094"
  },
  {
    "id": "C5679815",
    "id2": "MedGen UID:1826165",
    "medgen_label": "Mucopolysaccharidosis type 2, attenuated form",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1826165",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016316",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016316",
    "nando_id": "NANDO:2201171"
  },
  {
    "id": "C5679972",
    "id2": "MedGen UID:1826169",
    "medgen_label": "Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1826169",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017695",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017695",
    "nando_id": "NANDO:2201159"
  },
  {
    "id": "CN201794",
    "id2": "MedGen UID:831252",
    "medgen_label": "Adult-onset citrullinemia type I",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/831252",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016601",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016601",
    "nando_id": "NANDO:2201095"
  },
  {
    "id": "C0162531",
    "id2": "MedGen UID:57931",
    "medgen_label": "Hereditary coproporphyria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/57931",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007369",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007369",
    "nando_id": "NANDO:2201264"
  },
  {
    "id": "C0162532",
    "id2": "MedGen UID:58118",
    "medgen_label": "Variegate porphyria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/58118",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008297",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008297",
    "nando_id": "NANDO:2201265"
  },
  {
    "id": "C0162565",
    "id2": "MedGen UID:56452",
    "medgen_label": "Acute intermittent porphyria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/56452",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008294",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008294",
    "nando_id": "NANDO:2201263"
  },
  {
    "id": "C0162568",
    "id2": "MedGen UID:56455",
    "medgen_label": "Erythropoietic protoporphyria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/56455",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001676",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001676",
    "nando_id": "NANDO:2201266"
  },
  {
    "id": "C0268250",
    "id2": "MedGen UID:78652",
    "medgen_label": "Gaucher disease type II",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78652",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009266",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009266",
    "nando_id": "NANDO:2201211"
  },
  {
    "id": "C0268251",
    "id2": "MedGen UID:78653",
    "medgen_label": "Gaucher disease type III",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78653",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009267",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009267",
    "nando_id": "NANDO:2201212"
  },
  {
    "id": "C0268262",
    "id2": "MedGen UID:120624",
    "medgen_label": "Sphingolipid activator protein 1 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120624",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009590",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009590",
    "nando_id": "NANDO:2201205"
  },
  {
    "id": "C0268271",
    "id2": "MedGen UID:75665",
    "medgen_label": "Infantile GM1 gangliosidosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75665",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009260",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009260",
    "nando_id": "NANDO:2201196"
  },
  {
    "id": "C0268272",
    "id2": "MedGen UID:120625",
    "medgen_label": "GM1 gangliosidosis type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120625",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009261",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009261",
    "nando_id": "NANDO:2201197"
  },
  {
    "id": "C0268273",
    "id2": "MedGen UID:78655",
    "medgen_label": "GM1 gangliosidosis type 3",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78655",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009262",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009262",
    "nando_id": "NANDO:2201198"
  },
  {
    "id": "C0268337",
    "id2": "MedGen UID:75670",
    "medgen_label": "Ehlers-Danlos syndrome, type 3",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75670",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007523",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007523",
    "nando_id": "NANDO:2201257"
  },
  {
    "id": "C0268626",
    "id2": "MedGen UID:75701",
    "medgen_label": "Juvenile nephropathic cystinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75701",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009066",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009066",
    "nando_id": "NANDO:2201235"
  },
  {
    "id": "C4225429",
    "id2": "MedGen UID:909864",
    "medgen_label": "Ehlers-Danlos syndrome, classic type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/909864",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007522",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007522",
    "nando_id": "NANDO:2201256"
  },
  {
    "id": "C4282398",
    "id2": "MedGen UID:924303",
    "medgen_label": "Sialidosis type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/924303",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009738",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009738",
    "nando_id": "NANDO:2201192"
  },
  {
    "id": "C4282398",
    "id2": "MedGen UID:924303",
    "medgen_label": "Sialidosis type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/924303",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009738",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009738",
    "nando_id": "NANDO:2201193"
  },
  {
    "id": "C4692546",
    "id2": "MedGen UID:1643471",
    "medgen_label": "Protoporphyria, erythropoietic, 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1643471",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0008319",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008319",
    "nando_id": "NANDO:2201266"
  },
  {
    "id": "C0086649",
    "id2": "MedGen UID:39477",
    "medgen_label": "Mucopolysaccharidosis, MPS-III-C",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/39477",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009657",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009657",
    "nando_id": "NANDO:2201176"
  },
  {
    "id": "C0086650",
    "id2": "MedGen UID:88602",
    "medgen_label": "Mucopolysaccharidosis, MPS-III-D",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/88602",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009658",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009658",
    "nando_id": "NANDO:2201177"
  },
  {
    "id": "C0086651",
    "id2": "MedGen UID:43375",
    "medgen_label": "Mucopolysaccharidosis, MPS-IV-A",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/43375",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009659",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009659",
    "nando_id": "NANDO:2201178"
  },
  {
    "id": "C0086652",
    "id2": "MedGen UID:43376",
    "medgen_label": "Mucopolysaccharidosis, MPS-IV-B",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/43376",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009660",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009660",
    "nando_id": "NANDO:2201179"
  },
  {
    "id": "C4551623",
    "id2": "MedGen UID:1645042",
    "medgen_label": "Ehlers-Danlos syndrome, arthrochalasia type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1645042",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007525",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007525",
    "nando_id": "NANDO:2201260"
  },
  {
    "id": "C1876161",
    "id2": "MedGen UID:406281",
    "medgen_label": "Neuronal ceroid lipofuscinosis 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/406281",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0008769",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008769",
    "nando_id": "NANDO:2201242"
  },
  {
    "id": "C1961835",
    "id2": "MedGen UID:409531",
    "medgen_label": "Gaucher disease type I",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/409531",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009265",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009265",
    "nando_id": "NANDO:2201210"
  },
  {
    "id": "C2700425",
    "id2": "MedGen UID:397792",
    "medgen_label": "Ehlers-Danlos syndrome, dermatosparaxis type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/397792",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009161",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009161",
    "nando_id": "NANDO:2201261"
  },
  {
    "id": "C2931013",
    "id2": "MedGen UID:419313",
    "medgen_label": "Ocular cystinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/419313",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009064",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009064",
    "nando_id": "NANDO:2201236"
  },
  {
    "id": "C0751276",
    "id2": "MedGen UID:155528",
    "medgen_label": "Metachromatic leukodystrophy, juvenile type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155528",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009591",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009591",
    "nando_id": "NANDO:2201203"
  },
  {
    "id": "C4048196",
    "id2": "MedGen UID:888408",
    "medgen_label": "Beta-D-mannosidosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/888408",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009562",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009562",
    "nando_id": "NANDO:2201190"
  },
  {
    "id": "C5681331",
    "id2": "MedGen UID:1826154",
    "medgen_label": "Inherited aplastic anemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1826154",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0001713",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0001713",
    "nando_id": "NANDO:2201275"
  },
  {
    "id": "C1850451",
    "id2": "MedGen UID:340540",
    "medgen_label": "Neuronal ceroid lipofuscinosis 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/340540",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0009744",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009744",
    "nando_id": "NANDO:2201241"
  },
  {
    "id": "C0002312",
    "id2": "MedGen UID:1434",
    "medgen_label": "alpha Thalassemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1434",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011399",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011399",
    "nando_id": "NANDO:2201273"
  },
  {
    "id": "C0005283",
    "id2": "MedGen UID:2611",
    "medgen_label": "beta Thalassemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/2611",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019402",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019402",
    "nando_id": "NANDO:2201274"
  },
  {
    "id": "C0008384",
    "id2": "MedGen UID:40266",
    "medgen_label": "Cholesteryl ester storage disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/40266",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019149",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019149",
    "nando_id": "NANDO:2201233"
  },
  {
    "id": "C0162530",
    "id2": "MedGen UID:102408",
    "medgen_label": "Cutaneous porphyria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/102408",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009902",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009902",
    "nando_id": "NANDO:2201268"
  },
  {
    "id": "C0162566",
    "id2": "MedGen UID:56453",
    "medgen_label": "Porphyria cutanea tarda",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/56453",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015104",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015104",
    "nando_id": "NANDO:2201267"
  },
  {
    "id": "C0162569",
    "id2": "MedGen UID:57940",
    "medgen_label": "Hepatoerythropoietic porphyria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/57940",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019799",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019799",
    "nando_id": "NANDO:2201270"
  },
  {
    "id": "C1970859",
    "id2": "MedGen UID:370369",
    "medgen_label": "X-linked Mendelian susceptibility to mycobacterial diseases due to CYBB deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/370369",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010389",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010389",
    "nando_id": "NANDO:2201279"
  },
  {
    "id": "C2026514",
    "id2": "MedGen UID:1708324",
    "medgen_label": "X-linked cerebral adrenoleukodystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1708324",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010247",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010247",
    "nando_id": "NANDO:2201246"
  },
  {
    "id": "C2677889",
    "id2": "MedGen UID:394385",
    "medgen_label": "X-linked erythropoietic protoporphyria",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/394385",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010420",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010420",
    "nando_id": "NANDO:2201269"
  },
  {
    "id": "C2931251",
    "id2": "MedGen UID:419756",
    "medgen_label": "Alpha-mannosidosis type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/419756",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0022424",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0022424",
    "nando_id": "NANDO:2201188"
  },
  {
    "id": "C0022797",
    "id2": "MedGen UID:7230",
    "medgen_label": "Adult neuronal ceroid lipofuscinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/7230",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019260",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019260",
    "nando_id": "NANDO:2201244"
  },
  {
    "id": "C0023806",
    "id2": "MedGen UID:44174",
    "medgen_label": "Sialidosis type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44174",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019346",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019346",
    "nando_id": "NANDO:2201191"
  },
  {
    "id": "C0268242",
    "id2": "MedGen UID:78650",
    "medgen_label": "Niemann-Pick disease, type A",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78650",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009756",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009756",
    "nando_id": "NANDO:2201206"
  },
  {
    "id": "C0268243",
    "id2": "MedGen UID:78651",
    "medgen_label": "Niemann-Pick disease, type B",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78651",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011871",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011871",
    "nando_id": "NANDO:2201207"
  },
  {
    "id": "C0268252",
    "id2": "MedGen UID:120623",
    "medgen_label": "Adult Krabbe disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120623",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016091",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016091",
    "nando_id": "NANDO:2201219"
  },
  {
    "id": "C0268263",
    "id2": "MedGen UID:75664",
    "medgen_label": "Multiple sulfatase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75664",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0010088",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010088",
    "nando_id": "NANDO:2201227"
  },
  {
    "id": "C0268263",
    "id2": "MedGen UID:75664",
    "medgen_label": "Multiple sulfatase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75664",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0010088",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010088",
    "nando_id": "NANDO:2201228"
  },
  {
    "id": "C0268275",
    "id2": "MedGen UID:78657",
    "medgen_label": "Tay-Sachs disease, variant AB",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78657",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010099",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010099",
    "nando_id": "NANDO:2201201"
  },
  {
    "id": "C0268281",
    "id2": "MedGen UID:75666",
    "medgen_label": "Infantile neuronal ceroid lipofuscinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75666",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019261",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019261",
    "nando_id": "NANDO:2201241"
  },
  {
    "id": "C0268338",
    "id2": "MedGen UID:82790",
    "medgen_label": "Ehlers-Danlos syndrome, type 4",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82790",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017314",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017314",
    "nando_id": "NANDO:2201258"
  },
  {
    "id": "C0268342",
    "id2": "MedGen UID:75672",
    "medgen_label": "Ehlers-Danlos syndrome, kyphoscoliotic type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75672",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0016002",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016002",
    "nando_id": "NANDO:2201259"
  },
  {
    "id": "C0348890",
    "id2": "MedGen UID:87595",
    "medgen_label": "Idiopathic aplastic anemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/87595",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012197",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012197",
    "nando_id": "NANDO:2201276"
  },
  {
    "id": "C1096902",
    "id2": "MedGen UID:203367",
    "medgen_label": "Sialic acid storage disease, severe infantile type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/203367",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010027",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010027",
    "nando_id": "NANDO:2201237"
  },
  {
    "id": "C3537440",
    "id2": "MedGen UID:760976",
    "medgen_label": "Infantile nephropathic cystinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/760976",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018467",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018467",
    "nando_id": "NANDO:2201234"
  },
  {
    "id": "C0342881",
    "id2": "MedGen UID:575266",
    "medgen_label": "Homozygous familial hypercholesterolemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/575266",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018328",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018328",
    "nando_id": "NANDO:2201255"
  },
  {
    "id": "C3888924",
    "id2": "MedGen UID:923868",
    "medgen_label": "Glycogen storage disease due to acid maltase deficiency, infantile onset",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/923868",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017694",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017694",
    "nando_id": "NANDO:2201229"
  },
  {
    "id": "C0036161",
    "id2": "MedGen UID:11313",
    "medgen_label": "Sandhoff disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/11313",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010006",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010006",
    "nando_id": "NANDO:2201200"
  },
  {
    "id": "C0039373",
    "id2": "MedGen UID:11713",
    "medgen_label": "Tay-Sachs disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/11713",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010100",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010100",
    "nando_id": "NANDO:2201199"
  },
  {
    "id": "C0043208",
    "id2": "MedGen UID:53088",
    "medgen_label": "Wolman disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/53088",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019148",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019148",
    "nando_id": "NANDO:2201232"
  },
  {
    "id": "C0271907",
    "id2": "MedGen UID:543648",
    "medgen_label": "Acquired aplastic anemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/543648",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015610",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015610",
    "nando_id": "NANDO:2201277"
  },
  {
    "id": "C1866294",
    "id2": "MedGen UID:356497",
    "medgen_label": "Ehlers-Danlos syndrome, musculocontractural type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/356497",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011142",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011142",
    "nando_id": "NANDO:2201262"
  },
  {
    "id": "C2931187",
    "id2": "MedGen UID:419735",
    "medgen_label": "Nephropathic cystinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/419735",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0100151",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0100151",
    "nando_id": "NANDO:2201234"
  },
  {
    "id": "C0022340",
    "id2": "MedGen UID:9589",
    "medgen_label": "Late-infantile neuronal ceroid lipofuscinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9589",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015674",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015674",
    "nando_id": "NANDO:2201242"
  },
  {
    "id": "C0751273",
    "id2": "MedGen UID:148270",
    "medgen_label": "Infantile Krabbe disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/148270",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016089",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016089",
    "nando_id": "NANDO:2201216"
  },
  {
    "id": "C0751278",
    "id2": "MedGen UID:155529",
    "medgen_label": "Metachromatic leukodystrophy, late infantile form",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155529",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017729",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017729",
    "nando_id": "NANDO:2201202"
  },
  {
    "id": "C0751279",
    "id2": "MedGen UID:199625",
    "medgen_label": "Metachromatic leukodystrophy, adult type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/199625",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017730",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017730",
    "nando_id": "NANDO:2201204"
  },
  {
    "id": "C1527231",
    "id2": "MedGen UID:315918",
    "medgen_label": "Adrenomyeloneuropathy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/315918",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015339",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015339",
    "nando_id": "NANDO:2201248"
  },
  {
    "id": "C5679974",
    "id2": "MedGen UID:1843432",
    "medgen_label": "Alpha-mannosidosis, adult form",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1843432",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017733",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017733",
    "nando_id": "NANDO:2201189"
  },
  {
    "id": "C5680869",
    "id2": "MedGen UID:1826101",
    "medgen_label": "Niemann-Pick disease type C, adult neurologic onset",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1826101",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016310",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016310",
    "nando_id": "NANDO:2201209"
  },
  {
    "id": "C5681076",
    "id2": "MedGen UID:1843217",
    "medgen_label": "Intermediate severe Salla disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1843217",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017737",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017737",
    "nando_id": "NANDO:2201238"
  },
  {
    "id": "CN293564",
    "id2": "MedGen UID:978346",
    "medgen_label": "Juvenile neuronal ceroid lipofuscinosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/978346",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019262",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019262",
    "nando_id": "NANDO:2201243"
  },
  {
    "id": "C1835437",
    "id2": "MedGen UID:331974",
    "medgen_label": "Platyspondylic dysplasia, Torrance type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/331974",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007895",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007895",
    "nando_id": "NANDO:2201347"
  },
  {
    "id": "C0205711",
    "id2": "MedGen UID:61440",
    "medgen_label": "Pelizaeus-Merzbacher disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/61440",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010714",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010714",
    "nando_id": "NANDO:2201288"
  },
  {
    "id": "C0220685",
    "id2": "MedGen UID:66315",
    "medgen_label": "Achondrogenesis type II",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/66315",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008702",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008702",
    "nando_id": "NANDO:2201345"
  },
  {
    "id": "C0410539",
    "id2": "MedGen UID:96080",
    "medgen_label": "Craniodiaphyseal dysplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/96080",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009031",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009031",
    "nando_id": "NANDO:2201368"
  },
  {
    "id": "C2020284",
    "id2": "MedGen UID:810955",
    "medgen_label": "Stickler syndrome type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/810955",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007160",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007160",
    "nando_id": "NANDO:2201354"
  },
  {
    "id": "C2675179",
    "id2": "MedGen UID:436367",
    "medgen_label": "Arginine:glycine amidinotransferase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/436367",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012996",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012996",
    "nando_id": "NANDO:2201299"
  },
  {
    "id": "C2676243",
    "id2": "MedGen UID:390993",
    "medgen_label": "Leukoencephalopathy-ataxia-hypodontia-hypomyelination syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/390993",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011897",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011897",
    "nando_id": "NANDO:2201297"
  },
  {
    "id": "C2676244",
    "id2": "MedGen UID:436642",
    "medgen_label": "Hypomyelinating leukodystrophy 6",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/436642",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012905",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012905",
    "nando_id": "NANDO:2201290"
  },
  {
    "id": "C2677109",
    "id2": "MedGen UID:383026",
    "medgen_label": "Hypomyelinating leukodystrophy 4",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/383026",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012824",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012824",
    "nando_id": "NANDO:2201293"
  },
  {
    "id": "C2986717",
    "id2": "MedGen UID:458943",
    "medgen_label": "Anti-NMDA receptor encephalitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/458943",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0021081",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0021081",
    "nando_id": "NANDO:2201317"
  },
  {
    "id": "C3149631",
    "id2": "MedGen UID:460981",
    "medgen_label": "Melorheostosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/460981",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007970",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007970",
    "nando_id": "NANDO:2201364"
  },
  {
    "id": "C3151409",
    "id2": "MedGen UID:462759",
    "medgen_label": "Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 3",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/462759",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013507",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013507",
    "nando_id": "NANDO:2201283"
  },
  {
    "id": "C0027873",
    "id2": "MedGen UID:45063",
    "medgen_label": "Neuromyelitis optica",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/45063",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019100",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019100",
    "nando_id": "NANDO:2201322"
  },
  {
    "id": "C0268374",
    "id2": "MedGen UID:82798",
    "medgen_label": "Junctional epidermolysis bullosa, non-Herlitz type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82798",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009180",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009180",
    "nando_id": "NANDO:2201379"
  },
  {
    "id": "C0432214",
    "id2": "MedGen UID:609409",
    "medgen_label": "Namaqualand hip dysplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/609409",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011496",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011496",
    "nando_id": "NANDO:2201352"
  },
  {
    "id": "C0432224",
    "id2": "MedGen UID:98147",
    "medgen_label": "Chondrodysplasia punctata, MT type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/98147",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007322",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007322",
    "nando_id": "NANDO:2201359"
  },
  {
    "id": "C0432262",
    "id2": "MedGen UID:98150",
    "medgen_label": "Dysosteosclerosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/98150",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009138",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009138",
    "nando_id": "NANDO:2201365"
  },
  {
    "id": "C0432443",
    "id2": "MedGen UID:96605",
    "medgen_label": "Deletion of long arm of chromosome 18",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/96605",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011147",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011147",
    "nando_id": "NANDO:2201291"
  },
  {
    "id": "C0542428",
    "id2": "MedGen UID:107448",
    "medgen_label": "Hypochondrogenesis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/107448",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019669",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019669",
    "nando_id": "NANDO:2201346"
  },
  {
    "id": "C1096903",
    "id2": "MedGen UID:203368",
    "medgen_label": "Salla disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/203368",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011449",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011449",
    "nando_id": "NANDO:2201294"
  },
  {
    "id": "C1856245",
    "id2": "MedGen UID:383869",
    "medgen_label": "Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/383869",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009310",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009310",
    "nando_id": "NANDO:2201282"
  },
  {
    "id": "C1856251",
    "id2": "MedGen UID:341102",
    "medgen_label": "Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/341102",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009309",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009309",
    "nando_id": "NANDO:2201281"
  },
  {
    "id": "C1856255",
    "id2": "MedGen UID:383872",
    "medgen_label": "Granulomatous disease, chronic, autosomal recessive, cytochrome b-negative",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/383872",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009308",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009308",
    "nando_id": "NANDO:2201280"
  },
  {
    "id": "C3669395",
    "id2": "MedGen UID:777171",
    "medgen_label": "X-linked chondrodysplasia punctata 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/777171",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010555",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010555",
    "nando_id": "NANDO:2201360"
  },
  {
    "id": "C3669395",
    "id2": "MedGen UID:777171",
    "medgen_label": "X-linked chondrodysplasia punctata 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/777171",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0010555",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010555",
    "nando_id": "NANDO:2201356"
  },
  {
    "id": "C4274084",
    "id2": "MedGen UID:894734",
    "medgen_label": "Pelizaeus Merzbacher like disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/894734",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017226",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017226",
    "nando_id": "NANDO:2201289"
  },
  {
    "id": "C0079298",
    "id2": "MedGen UID:86896",
    "medgen_label": "Epidermolysis bullosa simplex",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/86896",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017610",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017610",
    "nando_id": "NANDO:2201341"
  },
  {
    "id": "C0079298",
    "id2": "MedGen UID:86896",
    "medgen_label": "Epidermolysis bullosa simplex",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/86896",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0017610",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017610",
    "nando_id": "NANDO:2201375"
  },
  {
    "id": "C0079301",
    "id2": "MedGen UID:86898",
    "medgen_label": "Junctional epidermolysis bullosa",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/86898",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017612",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017612",
    "nando_id": "NANDO:2201342"
  },
  {
    "id": "C0079474",
    "id2": "MedGen UID:36311",
    "medgen_label": "Recessive dystrophic epidermolysis bullosa",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/36311",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009179",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009179",
    "nando_id": "NANDO:2201383"
  },
  {
    "id": "C0079683",
    "id2": "MedGen UID:36328",
    "medgen_label": "Junctional epidermolysis bullosa gravis of Herlitz",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/36328",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009182",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009182",
    "nando_id": "NANDO:2201378"
  },
  {
    "id": "C0700635",
    "id2": "MedGen UID:147134",
    "medgen_label": "Spondyloepimetaphyseal dysplasia, Strudwick type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/147134",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008476",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008476",
    "nando_id": "NANDO:2201349"
  },
  {
    "id": "C1836683",
    "id2": "MedGen UID:324580",
    "medgen_label": "Spondyloepiphyseal dysplasia with metatarsal shortening",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/324580",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012206",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012206",
    "nando_id": "NANDO:2201353"
  },
  {
    "id": "C1836727",
    "id2": "MedGen UID:373160",
    "medgen_label": "PCWH syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/373160",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012198",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012198",
    "nando_id": "NANDO:2201298"
  },
  {
    "id": "C1845862",
    "id2": "MedGen UID:337451",
    "medgen_label": "Creatine transporter deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/337451",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010305",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010305",
    "nando_id": "NANDO:2201301"
  },
  {
    "id": "C5676875",
    "id2": "MedGen UID:1810975",
    "medgen_label": "Junctional epidermolysis bullosa with pyloric atresia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1810975",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009183",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009183",
    "nando_id": "NANDO:2201380"
  },
  {
    "id": "C0282102",
    "id2": "MedGen UID:79381",
    "medgen_label": "Chondrodysplasia punctata 2 X-linked dominant",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/79381",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020603",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020603",
    "nando_id": "NANDO:2201357"
  },
  {
    "id": "C1864663",
    "id2": "MedGen UID:501134",
    "medgen_label": "Hypomyelination and Congenital Cataract",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/501134",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012514",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012514",
    "nando_id": "NANDO:2201296"
  },
  {
    "id": "C2745959",
    "id2": "MedGen UID:412530",
    "medgen_label": "Spondyloepiphyseal dysplasia congenita",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/412530",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008471",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008471",
    "nando_id": "NANDO:2201348"
  },
  {
    "id": "C2931048",
    "id2": "MedGen UID:418969",
    "medgen_label": "Greenberg dysplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/418969",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008974",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008974",
    "nando_id": "NANDO:2201361"
  },
  {
    "id": "C2931072",
    "id2": "MedGen UID:418981",
    "medgen_label": "Epidermolysis bullosa simplex 5B, with muscular dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/418981",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009181",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009181",
    "nando_id": "NANDO:2201376"
  },
  {
    "id": "C4511620",
    "id2": "MedGen UID:1377523",
    "medgen_label": "Autosomal dominant medullary cystic kidney disease with or without hyperuricemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1377523",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008264",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008264",
    "nando_id": "NANDO:2201386"
  },
  {
    "id": "C0265260",
    "id2": "MedGen UID:75557",
    "medgen_label": "Grebe syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75557",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0008703",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008703",
    "nando_id": "NANDO:2201346"
  },
  {
    "id": "C0265260",
    "id2": "MedGen UID:75557",
    "medgen_label": "Grebe syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75557",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0008703",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008703",
    "nando_id": "NANDO:2201345"
  },
  {
    "id": "C0265279",
    "id2": "MedGen UID:75559",
    "medgen_label": "Kniest dysplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75559",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007987",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007987",
    "nando_id": "NANDO:2201350"
  },
  {
    "id": "C0265292",
    "id2": "MedGen UID:82702",
    "medgen_label": "Craniometaphyseal dysplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82702",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015465",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015465",
    "nando_id": "NANDO:2201366"
  },
  {
    "id": "C0265294",
    "id2": "MedGen UID:82704",
    "medgen_label": "Pyle metaphyseal dysplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82704",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009943",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009943",
    "nando_id": "NANDO:2201367"
  },
  {
    "id": "C0265301",
    "id2": "MedGen UID:120530",
    "medgen_label": "Sclerosteosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120530",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017838",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017838",
    "nando_id": "NANDO:2201369"
  },
  {
    "id": "C0559459",
    "id2": "MedGen UID:107852",
    "medgen_label": "Sacrococcygeal teratoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/107852",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0042727",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0042727",
    "nando_id": "NANDO:2201287"
  },
  {
    "id": "C0574080",
    "id2": "MedGen UID:154356",
    "medgen_label": "Deficiency of guanidinoacetate methyltransferase",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/154356",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012999",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012999",
    "nando_id": "NANDO:2201300"
  },
  {
    "id": "C0751964",
    "id2": "MedGen UID:155968",
    "medgen_label": "Primary progressive multiple sclerosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155968",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000451",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000451",
    "nando_id": "NANDO:2201320"
  },
  {
    "id": "C0751965",
    "id2": "MedGen UID:155969",
    "medgen_label": "Secondary progressive multiple sclerosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155969",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000450",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000450",
    "nando_id": "NANDO:2201321"
  },
  {
    "id": "C0751967",
    "id2": "MedGen UID:155669",
    "medgen_label": "Relapsing remitting multiple sclerosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155669",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005314",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005314",
    "nando_id": "NANDO:2201319"
  },
  {
    "id": "C0795889",
    "id2": "MedGen UID:208645",
    "medgen_label": "Allan-Herndon-Dudley syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/208645",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010354",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010354",
    "nando_id": "NANDO:2201292"
  },
  {
    "id": "C0795949",
    "id2": "MedGen UID:167086",
    "medgen_label": "Galloway-Mowat syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/167086",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009627",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009627",
    "nando_id": "NANDO:2201385"
  },
  {
    "id": "C0796173",
    "id2": "MedGen UID:163223",
    "medgen_label": "Spondyloperipheral dysplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/163223",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010078",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010078",
    "nando_id": "NANDO:2201351"
  },
  {
    "id": "C1300228",
    "id2": "MedGen UID:224886",
    "medgen_label": "Astley-Kendall dysplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/224886",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019408",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019408",
    "nando_id": "NANDO:2201362"
  },
  {
    "id": "CN236409",
    "id2": "MedGen UID:880851",
    "medgen_label": "Interfrontal craniofaciosynostosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/880851",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018065",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018065",
    "nando_id": "NANDO:2201305"
  },
  {
    "id": "C1609433",
    "id2": "MedGen UID:296299",
    "medgen_label": "Bilateral renal agenesis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/296299",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015986",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015986",
    "nando_id": "NANDO:2201462"
  },
  {
    "id": "C1848137",
    "id2": "MedGen UID:338393",
    "medgen_label": "Developmental and epileptic encephalopathy, 9",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/338393",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010246",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010246",
    "nando_id": "NANDO:2201404"
  },
  {
    "id": "C1849508",
    "id2": "MedGen UID:340341",
    "medgen_label": "Pyridoxine-dependent epilepsy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/340341",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009945",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009945",
    "nando_id": "NANDO:2201409"
  },
  {
    "id": "C1853271",
    "id2": "MedGen UID:501133",
    "medgen_label": "Autosomal recessive hypophosphatemic bone disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/501133",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009431",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009431",
    "nando_id": "NANDO:2201479"
  },
  {
    "id": "C1854630",
    "id2": "MedGen UID:340266",
    "medgen_label": "Wiedemann-Steiner syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/340266",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011518",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011518",
    "nando_id": "NANDO:2201417"
  },
  {
    "id": "C0175713",
    "id2": "MedGen UID:61236",
    "medgen_label": "Aicardi syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/61236",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010568",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010568",
    "nando_id": "NANDO:2201397"
  },
  {
    "id": "C0220989",
    "id2": "MedGen UID:66352",
    "medgen_label": "Acquired partial lipodystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/66352",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012104",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012104",
    "nando_id": "NANDO:2201447"
  },
  {
    "id": "C0221032",
    "id2": "MedGen UID:67438",
    "medgen_label": "Congenital generalized lipodystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/67438",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0006536",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0006536",
    "nando_id": "NANDO:2201444"
  },
  {
    "id": "C1970431",
    "id2": "MedGen UID:370910",
    "medgen_label": "Pitt-Hopkins syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/370910",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012589",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012589",
    "nando_id": "NANDO:2201419"
  },
  {
    "id": "C2677903",
    "id2": "MedGen UID:437070",
    "medgen_label": "Syndromic X-linked intellectual disability Najm type",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/437070",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010417",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010417",
    "nando_id": "NANDO:2201393"
  },
  {
    "id": "C3151411",
    "id2": "MedGen UID:462761",
    "medgen_label": "Intellectual disability, autosomal dominant 6",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/462761",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0013509",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013509",
    "nando_id": "NANDO:2201400"
  },
  {
    "id": "C5393299",
    "id2": "MedGen UID:1715418",
    "medgen_label": "Intellectual disability, X-linked 102",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1715418",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010497",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010497",
    "nando_id": "NANDO:2201395"
  },
  {
    "id": "C5848259",
    "id2": "MedGen UID:1845578",
    "medgen_label": "Werdnig-Hoffmann disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1845578",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009669",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009669",
    "nando_id": "NANDO:2201430"
  },
  {
    "id": "C0023976",
    "id2": "MedGen UID:44193",
    "medgen_label": "Long QT syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44193",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0002442",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002442",
    "nando_id": "NANDO:2201452"
  },
  {
    "id": "C0393538",
    "id2": "MedGen UID:95975",
    "medgen_label": "Spinal muscular atrophy, type II",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/95975",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009673",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009673",
    "nando_id": "NANDO:2201431"
  },
  {
    "id": "C1262481",
    "id2": "MedGen UID:220382",
    "medgen_label": "Eosinophilic gastroenteritis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/220382",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016129",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016129",
    "nando_id": "NANDO:2201440"
  },
  {
    "id": "C1274103",
    "id2": "MedGen UID:226893",
    "medgen_label": "Tumor-induced osteomalacia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/226893",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018124",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018124",
    "nando_id": "NANDO:2201480"
  },
  {
    "id": "C3489789",
    "id2": "MedGen UID:483742",
    "medgen_label": "Progressive familial intrahepatic cholestasis type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/483742",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011156",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011156",
    "nando_id": "NANDO:2201437"
  },
  {
    "id": "C3494976",
    "id2": "MedGen UID:782160",
    "medgen_label": "Malignant migrating partial seizures of infancy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/782160",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017385",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017385",
    "nando_id": "NANDO:2201408"
  },
  {
    "id": "C3550973",
    "id2": "MedGen UID:763887",
    "medgen_label": "Neurodegeneration with brain iron accumulation 5",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/763887",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010476",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010476",
    "nando_id": "NANDO:2201414"
  },
  {
    "id": "C4273131",
    "id2": "MedGen UID:1636666",
    "medgen_label": "Branchiootic syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1636666",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018878",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018878",
    "nando_id": "NANDO:2201391"
  },
  {
    "id": "C4749332",
    "id2": "MedGen UID:1669432",
    "medgen_label": "Proton-pump inhibitor-responsive esophageal eosinophilia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1669432",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018468",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018468",
    "nando_id": "NANDO:2201441"
  },
  {
    "id": "C4750837",
    "id2": "MedGen UID:1656239",
    "medgen_label": "Severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1656239",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014205",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014205",
    "nando_id": "NANDO:2201416"
  },
  {
    "id": "C0152109",
    "id2": "MedGen UID:101816",
    "medgen_label": "Kugelberg-Welander disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/101816",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009672",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009672",
    "nando_id": "NANDO:2201432"
  },
  {
    "id": "C0341106",
    "id2": "MedGen UID:83318",
    "medgen_label": "Eosinophilic esophagitis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/83318",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0005361",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0005361",
    "nando_id": "NANDO:2201439"
  },
  {
    "id": "C0342418",
    "id2": "MedGen UID:137970",
    "medgen_label": "Hamartoma of hypothalamus",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/137970",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009436",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009436",
    "nando_id": "NANDO:2201401"
  },
  {
    "id": "C1838230",
    "id2": "MedGen UID:325364",
    "medgen_label": "Spinal muscular atrophy, type IV",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/325364",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010056",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010056",
    "nando_id": "NANDO:2201433"
  },
  {
    "id": "C4015316",
    "id2": "MedGen UID:863753",
    "medgen_label": "Developmental and epileptic encephalopathy, 27",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/863753",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0014505",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014505",
    "nando_id": "NANDO:2201400"
  },
  {
    "id": "C4551898",
    "id2": "MedGen UID:1645830",
    "medgen_label": "Progressive familial intrahepatic cholestasis type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1645830",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008892",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008892",
    "nando_id": "NANDO:2201436"
  },
  {
    "id": "C0039743",
    "id2": "MedGen UID:21124",
    "medgen_label": "Thanatophoric dysplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21124",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017042",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017042",
    "nando_id": "NANDO:2201426"
  },
  {
    "id": "C0282512",
    "id2": "MedGen UID:79465",
    "medgen_label": "Landau-Kleffner syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/79465",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009509",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009509",
    "nando_id": "NANDO:2201429"
  },
  {
    "id": "C0282577",
    "id2": "MedGen UID:76469",
    "medgen_label": "Congenital disorder of glycosylation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/76469",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015286",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015286",
    "nando_id": "NANDO:2201396"
  },
  {
    "id": "C1864723",
    "id2": "MedGen UID:350498",
    "medgen_label": "Pyridoxal phosphate-responsive seizures",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/350498",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012407",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012407",
    "nando_id": "NANDO:2201411"
  },
  {
    "id": "C1865643",
    "id2": "MedGen UID:356333",
    "medgen_label": "Progressive familial intrahepatic cholestasis type 3",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/356333",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011214",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011214",
    "nando_id": "NANDO:2201438"
  },
  {
    "id": "C1868081",
    "id2": "MedGen UID:356898",
    "medgen_label": "Generalized juvenile polyposis/juvenile polyposis coli",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/356898",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0008276",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008276",
    "nando_id": "NANDO:2201454"
  },
  {
    "id": "C1868081",
    "id2": "MedGen UID:356898",
    "medgen_label": "Generalized juvenile polyposis/juvenile polyposis coli",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/356898",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0008276",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008276",
    "nando_id": "NANDO:2201457"
  },
  {
    "id": "C1868678",
    "id2": "MedGen UID:358383",
    "medgen_label": "Thanatophoric dysplasia type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/358383",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008546",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008546",
    "nando_id": "NANDO:2201427"
  },
  {
    "id": "C2750481",
    "id2": "MedGen UID:442490",
    "medgen_label": "Factor XIII, b subunit, deficiency of",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/442490",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013190",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013190",
    "nando_id": "NANDO:2201459"
  },
  {
    "id": "C2750514",
    "id2": "MedGen UID:442497",
    "medgen_label": "Factor XIII, A subunit, deficiency of",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/442497",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013187",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013187",
    "nando_id": "NANDO:2201460"
  },
  {
    "id": "C2751310",
    "id2": "MedGen UID:414347",
    "medgen_label": "Familial juvenile hyperuricemic nephropathy type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/414347",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013128",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013128",
    "nando_id": "NANDO:2201389"
  },
  {
    "id": "C4310741",
    "id2": "MedGen UID:934708",
    "medgen_label": "Hyperuricemic nephropathy, familial juvenile type 4",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/934708",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014891",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014891",
    "nando_id": "NANDO:2201390"
  },
  {
    "id": "C0019569",
    "id2": "MedGen UID:5559",
    "medgen_label": "Aganglionic megacolon",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5559",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018309",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018309",
    "nando_id": "NANDO:2201465"
  },
  {
    "id": "C0019569",
    "id2": "MedGen UID:5559",
    "medgen_label": "Aganglionic megacolon",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5559",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018309",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018309",
    "nando_id": "NANDO:2201464"
  },
  {
    "id": "C0019569",
    "id2": "MedGen UID:5559",
    "medgen_label": "Aganglionic megacolon",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5559",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018309",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018309",
    "nando_id": "NANDO:2201466"
  },
  {
    "id": "C0019569",
    "id2": "MedGen UID:5559",
    "medgen_label": "Aganglionic megacolon",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5559",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018309",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018309",
    "nando_id": "NANDO:2201463"
  },
  {
    "id": "C0019569",
    "id2": "MedGen UID:5559",
    "medgen_label": "Aganglionic megacolon",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5559",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0018309",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018309",
    "nando_id": "NANDO:2201467"
  },
  {
    "id": "C0019829",
    "id2": "MedGen UID:9283",
    "medgen_label": "Classic Hodgkin lymphoma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/9283",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009348",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009348",
    "nando_id": "NANDO:2201476"
  },
  {
    "id": "C0022387",
    "id2": "MedGen UID:5929",
    "medgen_label": "Jervell and Lange-Nielsen syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/5929",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002441",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002441",
    "nando_id": "NANDO:2201453"
  },
  {
    "id": "C0265223",
    "id2": "MedGen UID:78539",
    "medgen_label": "Cohen syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/78539",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008999",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008999",
    "nando_id": "NANDO:2201418"
  },
  {
    "id": "C0265234",
    "id2": "MedGen UID:82693",
    "medgen_label": "Melnick-Fraser syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82693",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007029",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007029",
    "nando_id": "NANDO:2201391"
  },
  {
    "id": "C0265264",
    "id2": "MedGen UID:120524",
    "medgen_label": "Holt-Oram syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120524",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007732",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007732",
    "nando_id": "NANDO:2201392"
  },
  {
    "id": "C0265482",
    "id2": "MedGen UID:489853",
    "medgen_label": "Ring chromosome 20 syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/489853",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015436",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015436",
    "nando_id": "NANDO:2201399"
  },
  {
    "id": "C0856761",
    "id2": "MedGen UID:163632",
    "medgen_label": "Budd-Chiari syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/163632",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010947",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010947",
    "nando_id": "NANDO:2201475"
  },
  {
    "id": "C1300257",
    "id2": "MedGen UID:226975",
    "medgen_label": "Thanatophoric dysplasia, type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/226975",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008547",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008547",
    "nando_id": "NANDO:2201428"
  },
  {
    "id": "C1527336",
    "id2": "MedGen UID:282890",
    "medgen_label": "Sjogren syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/282890",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0010030",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010030",
    "nando_id": "NANDO:2201468"
  },
  {
    "id": "CN262437",
    "id2": "MedGen UID:945467",
    "medgen_label": "Berardinelli-Seip congenital lipodystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/945467",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018883",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018883",
    "nando_id": "NANDO:2201444"
  },
  {
    "id": "C1704375",
    "id2": "MedGen UID:309957",
    "medgen_label": "Hypophosphatemic rickets",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/309957",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0024300",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0024300",
    "nando_id": "NANDO:2201477"
  },
  {
    "id": "C1833104",
    "id2": "MedGen UID:371484",
    "medgen_label": "Permanent neonatal diabetes mellitus",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/371484",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0100164",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0100164",
    "nando_id": "NANDO:2201435"
  },
  {
    "id": "C0221018",
    "id2": "MedGen UID:65119",
    "medgen_label": "Hereditary sideroblastic anemia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/65119",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020099",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020099",
    "nando_id": "NANDO:2201470"
  },
  {
    "id": "C0431391",
    "id2": "MedGen UID:140910",
    "medgen_label": "Hemimegalencephaly",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/140910",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020492",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020492",
    "nando_id": "NANDO:2201394"
  },
  {
    "id": "C0266294",
    "id2": "MedGen UID:75607",
    "medgen_label": "Unilateral renal agenesis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75607",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019636",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019636",
    "nando_id": "NANDO:2201461"
  },
  {
    "id": "C0393703",
    "id2": "MedGen UID:140741",
    "medgen_label": "Epilepsy with myoclonic absences",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/140741",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019487",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019487",
    "nando_id": "NANDO:2201406"
  },
  {
    "id": "C0393706",
    "id2": "MedGen UID:97959",
    "medgen_label": "Early infantile epileptic encephalopathy with suppression bursts",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/97959",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0100062",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0100062",
    "nando_id": "NANDO:2201398"
  },
  {
    "id": "C0342273",
    "id2": "MedGen UID:449530",
    "medgen_label": "Transitory neonatal diabetes mellitus",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/449530",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020525",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020525",
    "nando_id": "NANDO:2201434"
  },
  {
    "id": "C0036420",
    "id2": "MedGen UID:48586",
    "medgen_label": "Localized scleroderma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/48586",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019562",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019562",
    "nando_id": "NANDO:2201420"
  },
  {
    "id": "C0036420",
    "id2": "MedGen UID:48586",
    "medgen_label": "Localized scleroderma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/48586",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0019562",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019562",
    "nando_id": "NANDO:2201421"
  },
  {
    "id": "C0271693",
    "id2": "MedGen UID:543499",
    "medgen_label": "Acquired generalized lipodystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/543499",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019193",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019193",
    "nando_id": "NANDO:2201445"
  },
  {
    "id": "C0271694",
    "id2": "MedGen UID:124408",
    "medgen_label": "Familial partial lipodystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/124408",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020088",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020088",
    "nando_id": "NANDO:2201446"
  },
  {
    "id": "C1868139",
    "id2": "MedGen UID:358137",
    "medgen_label": "Tubulointerstitial kidney disease, autosomal dominant, 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/358137",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020726",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020726",
    "nando_id": "NANDO:2201388"
  },
  {
    "id": "C4316789",
    "id2": "MedGen UID:1386287",
    "medgen_label": "Partial lipodystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1386287",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0027767",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0027767",
    "nando_id": "NANDO:2201443"
  },
  {
    "id": "C4317112",
    "id2": "MedGen UID:1369615",
    "medgen_label": "Generalized lipodystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1369615",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0027766",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0027766",
    "nando_id": "NANDO:2201442"
  },
  {
    "id": "C4518639",
    "id2": "MedGen UID:1381392",
    "medgen_label": "Epilepsy of infancy with migrating focal seizures",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1381392",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0100025",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0100025",
    "nando_id": "NANDO:2201408"
  },
  {
    "id": "C5445164",
    "id2": "MedGen UID:1778573",
    "medgen_label": "Juvenile polyposis of infancy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1778573",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019190",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019190",
    "nando_id": "NANDO:2201458"
  },
  {
    "id": "C0263409",
    "id2": "MedGen UID:75518",
    "medgen_label": "Linear scleroderma",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75518",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0043294",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0043294",
    "nando_id": "NANDO:2201422"
  },
  {
    "id": "CN293409",
    "id2": "MedGen UID:976783",
    "medgen_label": "Pyridoxine-dependent epilepsy caused by ALDH7A1 mutant",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/976783",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020741",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020741",
    "nando_id": "NANDO:2201410"
  },
  {
    "id": "C1563715",
    "id2": "MedGen UID:327586",
    "medgen_label": "Andersen Tawil syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/327586",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008222",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008222",
    "nando_id": "NANDO:2201516"
  },
  {
    "id": "C1563715",
    "id2": "MedGen UID:327586",
    "medgen_label": "Andersen Tawil syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/327586",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008222",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008222",
    "nando_id": "NANDO:1201117"
  },
  {
    "id": "C1846386",
    "id2": "MedGen UID:375876",
    "medgen_label": "Isolated focal cortical dysplasia type IIa",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/375876",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017101",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017101",
    "nando_id": "NANDO:2201502"
  },
  {
    "id": "C1849453",
    "id2": "MedGen UID:336602",
    "medgen_label": "Rapadilino syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/336602",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009955",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009955",
    "nando_id": "NANDO:2201531"
  },
  {
    "id": "C0221055",
    "id2": "MedGen UID:113142",
    "medgen_label": "Paramyotonia congenita of Von Eulenburg",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/113142",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008195",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008195",
    "nando_id": "NANDO:2201512"
  },
  {
    "id": "C2931826",
    "id2": "MedGen UID:444151",
    "medgen_label": "Potassium-aggravated myotonia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/444151",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018959",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018959",
    "nando_id": "NANDO:2201513"
  },
  {
    "id": "C2936781",
    "id2": "MedGen UID:422446",
    "medgen_label": "Congenital myotonia, autosomal dominant form",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/422446",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008055",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008055",
    "nando_id": "NANDO:2201510"
  },
  {
    "id": "C5203410",
    "id2": "MedGen UID:1684753",
    "medgen_label": "Rothmund-Thomson syndrome type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1684753",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016369",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016369",
    "nando_id": "NANDO:2201529"
  },
  {
    "id": "C5231433",
    "id2": "MedGen UID:1684764",
    "medgen_label": "Rothmund-Thomson syndrome type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1684764",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016368",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016368",
    "nando_id": "NANDO:2201528"
  },
  {
    "id": "C5779872",
    "id2": "MedGen UID:1830421",
    "medgen_label": "Multiple congenital anomalies due to 14q32.2 maternally expressed gene defect",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1830421",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016779",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016779",
    "nando_id": "NANDO:2201523"
  },
  {
    "id": "C0028860",
    "id2": "MedGen UID:18145",
    "medgen_label": "Lowe syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/18145",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010645",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010645",
    "nando_id": "NANDO:1201116"
  },
  {
    "id": "C0030443",
    "id2": "MedGen UID:18291",
    "medgen_label": "Familial periodic paralysis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/18291",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0000995",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0000995",
    "nando_id": "NANDO:2100307"
  },
  {
    "id": "C3280976",
    "id2": "MedGen UID:482606",
    "medgen_label": "Thrombomodulin-related bleeding disorder",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/482606",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0013775",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013775",
    "nando_id": "NANDO:1201115"
  },
  {
    "id": "C4707795",
    "id2": "MedGen UID:1645432",
    "medgen_label": "Isolated focal cortical dysplasia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1645432",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019009",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019009",
    "nando_id": "NANDO:2201498"
  },
  {
    "id": "C4749399",
    "id2": "MedGen UID:1649806",
    "medgen_label": "Secondary syringomyelia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1649806",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0020509",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0020509",
    "nando_id": "NANDO:2201533"
  },
  {
    "id": "C3887523",
    "id2": "MedGen UID:854382",
    "medgen_label": "Very long chain acyl-CoA dehydrogenase deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/854382",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008723",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008723",
    "nando_id": "NANDO:1201109"
  },
  {
    "id": "C4014419",
    "id2": "MedGen UID:862856",
    "medgen_label": "AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/862856",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014358",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014358",
    "nando_id": "NANDO:2201524"
  },
  {
    "id": "C4014722",
    "id2": "MedGen UID:863159",
    "medgen_label": "STING-associated vasculopathy with onset in infancy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/863159",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014405",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014405",
    "nando_id": "NANDO:1201110"
  },
  {
    "id": "C4014722",
    "id2": "MedGen UID:863159",
    "medgen_label": "STING-associated vasculopathy with onset in infancy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/863159",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014405",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014405",
    "nando_id": "NANDO:2201487"
  },
  {
    "id": "C5575066",
    "id2": "MedGen UID:1807366",
    "medgen_label": "Schaaf-Yang syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1807366",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014243",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014243",
    "nando_id": "NANDO:2201525"
  },
  {
    "id": "C0032339",
    "id2": "MedGen UID:10819",
    "medgen_label": "Rothmund-Thomson syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10819",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010002",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010002",
    "nando_id": "NANDO:2201527"
  },
  {
    "id": "C0039144",
    "id2": "MedGen UID:21449",
    "medgen_label": "Syringomyelia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21449",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017987",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017987",
    "nando_id": "NANDO:2201488"
  },
  {
    "id": "C0040588",
    "id2": "MedGen UID:21228",
    "medgen_label": "Tracheoesophageal fistula",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/21228",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008586",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008586",
    "nando_id": "NANDO:2201517"
  },
  {
    "id": "C1868512",
    "id2": "MedGen UID:356995",
    "medgen_label": "Adult-onset autosomal dominant demyelinating leukodystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/356995",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008215",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008215",
    "nando_id": "NANDO:1201107"
  },
  {
    "id": "C2750067",
    "id2": "MedGen UID:412870",
    "medgen_label": "Congenital plasminogen activator inhibitor type 1 deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/412870",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0013227",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0013227",
    "nando_id": "NANDO:1201113"
  },
  {
    "id": "C2752081",
    "id2": "MedGen UID:414178",
    "medgen_label": "Alpha-2-plasmin inhibitor deficiency",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/414178",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009883",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009883",
    "nando_id": "NANDO:1201114"
  },
  {
    "id": "C0238357",
    "id2": "MedGen UID:68665",
    "medgen_label": "Familial hyperkalemic periodic paralysis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/68665",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008224",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008224",
    "nando_id": "NANDO:2201514"
  },
  {
    "id": "C0238358",
    "id2": "MedGen UID:116058",
    "medgen_label": "Hypokalemic periodic paralysis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/116058",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008223",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008223",
    "nando_id": "NANDO:2201515"
  },
  {
    "id": "C0242387",
    "id2": "MedGen UID:66078",
    "medgen_label": "Treacher Collins syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/66078",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002457",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002457",
    "nando_id": "NANDO:2201526"
  },
  {
    "id": "C0265308",
    "id2": "MedGen UID:120532",
    "medgen_label": "Baller-Gerold syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120532",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009039",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009039",
    "nando_id": "NANDO:2201530"
  },
  {
    "id": "C0751360",
    "id2": "MedGen UID:155852",
    "medgen_label": "Congenital myotonia, autosomal recessive form",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155852",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009715",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009715",
    "nando_id": "NANDO:2201511"
  },
  {
    "id": "C5679765",
    "id2": "MedGen UID:1842666",
    "medgen_label": "Isolated focal cortical dysplasia type Ib",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1842666",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017097",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017097",
    "nando_id": "NANDO:2201500"
  },
  {
    "id": "C5679767",
    "id2": "MedGen UID:1843115",
    "medgen_label": "Isolated focal cortical dysplasia type Ia",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1843115",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017096",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017096",
    "nando_id": "NANDO:2201499"
  },
  {
    "id": "C5679768",
    "id2": "MedGen UID:1842232",
    "medgen_label": "Isolated focal cortical dysplasia type IIb",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1842232",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0017102",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0017102",
    "nando_id": "NANDO:2201503"
  },
  {
    "id": "CN311573",
    "id2": "MedGen UID:992104",
    "medgen_label": "Thomsen and Becker disease",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/992104",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009710",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009710",
    "nando_id": "NANDO:2201509"
  },
  {
    "id": "CN924912",
    "id2": "MedGen UID:1564287",
    "medgen_label": "PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1564287",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014512",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014512",
    "nando_id": "NANDO:1201108"
  },
  {
    "id": "C1847640",
    "id2": "MedGen UID:338281",
    "medgen_label": "Kufor-Rakeb syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/338281",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011706",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011706",
    "nando_id": "NANDO:1201153"
  },
  {
    "id": "C5204115",
    "id2": "MedGen UID:1684787",
    "medgen_label": "AH amyloidosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1684787",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018613",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018613",
    "nando_id": "NANDO:1201122"
  },
  {
    "id": "C0024796",
    "id2": "MedGen UID:44287",
    "medgen_label": "Marfan syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/44287",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0007947",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007947",
    "nando_id": "NANDO:1201158"
  },
  {
    "id": "C0028968",
    "id2": "MedGen UID:10435",
    "medgen_label": "Olivopontocerebellar atrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/10435",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0002017",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0002017",
    "nando_id": "NANDO:1201119"
  },
  {
    "id": "C0268381",
    "id2": "MedGen UID:75674",
    "medgen_label": "AL amyloidosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/75674",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019438",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019438",
    "nando_id": "NANDO:1201121"
  },
  {
    "id": "C0270724",
    "id2": "MedGen UID:82852",
    "medgen_label": "Infantile neuroaxonal dystrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/82852",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0024457",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0024457",
    "nando_id": "NANDO:1201155"
  },
  {
    "id": "C0270733",
    "id2": "MedGen UID:124366",
    "medgen_label": "Striatonigral degeneration",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/124366",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0003122",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0003122",
    "nando_id": "NANDO:1201118"
  },
  {
    "id": "C0393571",
    "id2": "MedGen UID:98276",
    "medgen_label": "Multiple system atrophy",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/98276",
    "property": "http://www.w3.org/2004/02/skos/core#closeMatch",
    "mondo_id": "MONDO:0007803",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0007803",
    "nando_id": "NANDO:1201120"
  },
  {
    "id": "C1857747",
    "id2": "MedGen UID:346658",
    "medgen_label": "Neurodegeneration with brain iron accumulation 2B",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/346658",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0012444",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0012444",
    "nando_id": "NANDO:1201156"
  },
  {
    "id": "C3550973",
    "id2": "MedGen UID:763887",
    "medgen_label": "Neurodegeneration with brain iron accumulation 5",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/763887",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010476",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010476",
    "nando_id": "NANDO:1201150"
  },
  {
    "id": "C3554374",
    "id2": "MedGen UID:767288",
    "medgen_label": "Dystonia 24",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/767288",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014019",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014019",
    "nando_id": "NANDO:1201143"
  },
  {
    "id": "C3694531",
    "id2": "MedGen UID:854172",
    "medgen_label": "Glycogen storage disease IXa1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/854172",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0010598",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0010598",
    "nando_id": "NANDO:1201175"
  },
  {
    "id": "C3826988",
    "id2": "MedGen UID:819736",
    "medgen_label": "Juvenile polymyositis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/819736",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019734",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019734",
    "nando_id": "NANDO:1201133"
  },
  {
    "id": "C4225336",
    "id2": "MedGen UID:907580",
    "medgen_label": "Dystonia 27",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/907580",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014627",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014627",
    "nando_id": "NANDO:1201146"
  },
  {
    "id": "C4225341",
    "id2": "MedGen UID:904244",
    "medgen_label": "Myoclonic dystonia 26",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/904244",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014620",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014620",
    "nando_id": "NANDO:1201145"
  },
  {
    "id": "C0342286",
    "id2": "MedGen UID:83337",
    "medgen_label": "Woodhouse-Sakati syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/83337",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0009419",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0009419",
    "nando_id": "NANDO:1201154"
  },
  {
    "id": "C0751037",
    "id2": "MedGen UID:196713",
    "medgen_label": "Cockayne syndrome type 3",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/196713",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008998",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008998",
    "nando_id": "NANDO:1201165"
  },
  {
    "id": "C2697932",
    "id2": "MedGen UID:395827",
    "medgen_label": "Loeys-Dietz syndrome",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/395827",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018954",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018954",
    "nando_id": "NANDO:1201159"
  },
  {
    "id": "C4304411",
    "id2": "MedGen UID:930080",
    "medgen_label": "Xeroderma pigmentosum-Cockayne syndrome complex",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/930080",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016354",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016354",
    "nando_id": "NANDO:1201166"
  },
  {
    "id": "C4304670",
    "id2": "MedGen UID:930339",
    "medgen_label": "Dystonia 25",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/930339",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014033",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014033",
    "nando_id": "NANDO:1201144"
  },
  {
    "id": "C4310633",
    "id2": "MedGen UID:934600",
    "medgen_label": "Dystonia 28, childhood-onset",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/934600",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015004",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015004",
    "nando_id": "NANDO:1201147"
  },
  {
    "id": "C4310634",
    "id2": "MedGen UID:934601",
    "medgen_label": "Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/934601",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0015003",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0015003",
    "nando_id": "NANDO:1201148"
  },
  {
    "id": "C4517377",
    "id2": "MedGen UID:1387791",
    "medgen_label": "Neurodegeneration with brain iron accumulation 6",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1387791",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0014290",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0014290",
    "nando_id": "NANDO:1201151"
  },
  {
    "id": "C5438812",
    "id2": "MedGen UID:1726699",
    "medgen_label": "Pfeiffer syndrome type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1726699",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019659",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019659",
    "nando_id": "NANDO:1201160"
  },
  {
    "id": "C5438849",
    "id2": "MedGen UID:1761826",
    "medgen_label": "Pfeiffer syndrome type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1761826",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019660",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019660",
    "nando_id": "NANDO:1201161"
  },
  {
    "id": "C5438850",
    "id2": "MedGen UID:1748161",
    "medgen_label": "Pfeiffer syndrome type 3",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1748161",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019661",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019661",
    "nando_id": "NANDO:1201162"
  },
  {
    "id": "C5543312",
    "id2": "MedGen UID:1785079",
    "medgen_label": "Dystonia 30",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1785079",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0025691",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0025691",
    "nando_id": "NANDO:1201149"
  },
  {
    "id": "C0263666",
    "id2": "MedGen UID:120486",
    "medgen_label": "Childhood type dermatomyositis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/120486",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0008054",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0008054",
    "nando_id": "NANDO:1201132"
  },
  {
    "id": "C0751038",
    "id2": "MedGen UID:155487",
    "medgen_label": "Cockayne syndrome type 2",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155487",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019570",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019570",
    "nando_id": "NANDO:1201164"
  },
  {
    "id": "C0751039",
    "id2": "MedGen UID:155488",
    "medgen_label": "Cockayne syndrome type 1",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/155488",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0019569",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0019569",
    "nando_id": "NANDO:1201163"
  },
  {
    "id": "C0878682",
    "id2": "MedGen UID:168057",
    "medgen_label": "Deficiency of ferroxidase",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/168057",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0011426",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0011426",
    "nando_id": "NANDO:1201152"
  },
  {
    "id": "C5679845",
    "id2": "MedGen UID:1842484",
    "medgen_label": "Apolipoprotein A-II amyloidosis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1842484",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0016533",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0016533",
    "nando_id": "NANDO:1201125"
  },
  {
    "id": "C5680100",
    "id2": "MedGen UID:1826070",
    "medgen_label": "MYO5B-related progressive familial intrahepatic cholestasis",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/1826070",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0018804",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0018804",
    "nando_id": "NANDO:1201174"
  },
  {
    "id": "CN305473",
    "id2": "MedGen UID:987242",
    "medgen_label": "Peroxisomal single enzyme/protein defect",
    "original_disease": "http://www.ncbi.nlm.nih.gov/medgen/987242",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_id": "MONDO:0100257",
    "mondolink": "http://purl.obolibrary.org/obo/MONDO_0100257",
    "nando_id": "NANDO:1201169"
  }
]