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    "mondo_id": "MONDO:0000437",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "小脳性運動失調",
    "mondo_label_en": "cerebellar ataxia",
    "mondo_url": "https://monarchinitiative.org/MONDO:0000437"
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    "nando_id": "NANDO:1200055",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200055",
    "mondo_id": "MONDO:0002561",
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    "mondo_label_ja": "ライソゾーム病",
    "mondo_label_en": "lysosomal storage disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0002561"
  },
  {
    "nando_id": "NANDO:1200002",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200002",
    "mondo_id": "MONDO:0004976",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "筋萎縮性側索硬化症",
    "mondo_label_en": "amyotrophic lateral sclerosis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0004976"
  },
  {
    "nando_id": "NANDO:1100006",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1100006",
    "mondo_id": "MONDO:0005570",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "血液障害",
    "mondo_label_en": "hematologic disorder",
    "mondo_url": "https://monarchinitiative.org/MONDO:0005570"
  },
  {
    "nando_id": "NANDO:1200030",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200030",
    "mondo_id": "MONDO:0006702",
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    "mondo_label_ja": "慢性炎症性脱髄性多発根ニューロパチー",
    "mondo_label_en": "chronic inflammatory demyelinating polyradiculoneuropathy",
    "mondo_url": "https://monarchinitiative.org/MONDO:0006702"
  },
  {
    "nando_id": "NANDO:1200041",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200041",
    "mondo_id": "MONDO:0007182",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "マカド-ジョセフ病",
    "mondo_label_en": "Machado-Joseph disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0007182"
  },
  {
    "nando_id": "NANDO:1200044",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200044",
    "mondo_id": "MONDO:0007296",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "脊髄小脳失調症31型",
    "mondo_label_en": "spinocerebellar ataxia type 31",
    "mondo_url": "https://monarchinitiative.org/MONDO:0007296"
  },
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    "nando_id": "NANDO:1200043",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200043",
    "mondo_id": "MONDO:0007435",
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    "mondo_label_ja": "歯状核赤核淡蒼球ルイ体萎縮症",
    "mondo_label_en": "dentatorubral-pallidoluysian atrophy",
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    "nando_id": "NANDO:1200030",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200030",
    "mondo_id": "MONDO:0007691",
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    "mondo_label_ja": "ギラン・バレー症候群, 家族性",
    "mondo_label_en": "Guillain-Barre syndrome, familial",
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    "nando_id": "NANDO:1200012",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200012",
    "mondo_id": "MONDO:0007739",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "ハンチントン病",
    "mondo_label_en": "Huntington disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0007739"
  },
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    "nando_id": "NANDO:1200034",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200034",
    "mondo_id": "MONDO:0007803",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "多系統萎縮症",
    "mondo_label_en": "multiple system atrophy",
    "mondo_url": "https://monarchinitiative.org/MONDO:0007803"
  },
  {
    "nando_id": "NANDO:1200032",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200032",
    "mondo_id": "MONDO:0007827",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "封入体筋炎",
    "mondo_label_en": "inclusion body myositis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0007827"
  },
  {
    "nando_id": "NANDO:1200045",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200045",
    "mondo_id": "MONDO:0008119",
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    "mondo_label_ja": "脊髄小脳失調症1型",
    "mondo_label_en": "spinocerebellar ataxia type 1",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008119"
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    "nando_id": "NANDO:1200042",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200042",
    "mondo_id": "MONDO:0008457",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "脊髄小脳失調症6型",
    "mondo_label_en": "spinocerebellar ataxia type 6",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008457"
  },
  {
    "nando_id": "NANDO:1200046",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200046",
    "mondo_id": "MONDO:0008458",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "脊髄小脳失調症2型",
    "mondo_label_en": "spinocerebellar ataxia type 2",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008458"
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    "nando_id": "NANDO:1200014",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200014",
    "mondo_id": "MONDO:0008695",
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    "mondo_label_ja": "舞踏病-有棘赤血球症",
    "mondo_label_en": "chorea-acanthocytosis",
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    "nando_id": "NANDO:1200051",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200051",
    "mondo_id": "MONDO:0008842",
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    "mondo_label_ja": "運動失調, 早期発症, 眼球運動失行および低アルブミン血症を伴う",
    "mondo_label_en": "ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia",
    "mondo_url": "https://monarchinitiative.org/MONDO:0008842"
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    "nando_id": "NANDO:1200067",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200067",
    "mondo_id": "MONDO:0009260",
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    "mondo_label_ja": "GM1ガングリオシドーシス1型",
    "mondo_label_en": "GM1 gangliosidosis type 1",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009260"
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    "nando_id": "NANDO:1200068",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200068",
    "mondo_id": "MONDO:0009261",
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    "mondo_label_ja": "GM1ガングリオシドーシス2型",
    "mondo_label_en": "GM1 gangliosidosis type 2",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009261"
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    "nando_id": "NANDO:1200069",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200069",
    "mondo_id": "MONDO:0009262",
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    "mondo_label_ja": "GM1ガングリオシドーシス3型",
    "mondo_label_en": "GM1 gangliosidosis type 3",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009262"
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    "nando_id": "NANDO:1200057",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200057",
    "mondo_id": "MONDO:0009265",
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    "mondo_label_ja": "ゴーシェ病I型",
    "mondo_label_en": "Gaucher disease type I",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009265"
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    "nando_id": "NANDO:1200058",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200058",
    "mondo_id": "MONDO:0009266",
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    "mondo_label_ja": "ゴーシェ病II型",
    "mondo_label_en": "Gaucher disease type II",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009266"
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    "nando_id": "NANDO:1200059",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200059",
    "mondo_id": "MONDO:0009267",
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    "mondo_label_ja": "ゴーシェ病III型",
    "mondo_label_en": "Gaucher disease type III",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009267"
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    "nando_id": "NANDO:1200074",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200074",
    "mondo_id": "MONDO:0009499",
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    "mondo_label_ja": "クラッベ病",
    "mondo_label_en": "Krabbe disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009499"
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    "nando_id": "NANDO:1200080",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200080",
    "mondo_id": "MONDO:0009591",
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    "mondo_label_ja": "異染性白質ジストロフィー, 若年型",
    "mondo_label_en": "metachromatic leukodystrophy, juvenile form",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009591"
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    "nando_id": "NANDO:1200004",
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    "mondo_id": "MONDO:0009669",
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    "mondo_label_ja": "脊髄性筋萎縮症1型",
    "mondo_label_en": "spinal muscular atrophy, type 1",
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    "nando_id": "NANDO:1200006",
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    "mondo_id": "MONDO:0009672",
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    "mondo_label_ja": "脊髄性筋萎縮症III型",
    "mondo_label_en": "spinal muscular atrophy, type III",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009672"
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    "nando_id": "NANDO:1200005",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200005",
    "mondo_id": "MONDO:0009673",
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    "mondo_label_ja": "脊髄性筋萎縮症II型",
    "mondo_label_en": "spinal muscular atrophy, type II",
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    "nando_id": "NANDO:1200020",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200020",
    "mondo_id": "MONDO:0009688",
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    "mondo_label_ja": "重症筋無力症",
    "mondo_label_en": "myasthenia gravis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0009688"
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    "nando_id": "NANDO:1200061",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200061",
    "mondo_id": "MONDO:0009756",
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    "mondo_label_ja": "ニーマン・ピック病A型",
    "mondo_label_en": "Niemann-Pick disease type A",
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    "nando_id": "NANDO:1200072",
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    "mondo_id": "MONDO:0010006",
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    "mondo_label_ja": "サンドホフ病",
    "mondo_label_en": "Sandhoff disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0010006"
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    "nando_id": "NANDO:1200007",
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    "mondo_id": "MONDO:0010056",
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    "mondo_label_ja": "脊髄性筋萎縮症IV型",
    "mondo_label_en": "spinal muscular atrophy, type IV",
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    "nando_id": "NANDO:1200073",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200073",
    "mondo_id": "MONDO:0010099",
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    "mondo_label_ja": "テイ・サックス病AB変異体",
    "mondo_label_en": "Tay-Sachs disease AB variant",
    "mondo_url": "https://monarchinitiative.org/MONDO:0010099"
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    "nando_id": "NANDO:1200071",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200071",
    "mondo_id": "MONDO:0010100",
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    "mondo_label_ja": "テイ・サックス病",
    "mondo_label_en": "Tay-Sachs disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0010100"
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    "nando_id": "NANDO:1200050",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200050",
    "mondo_id": "MONDO:0010188",
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    "mondo_label_en": "familial isolated deficiency of vitamin E",
    "mondo_url": "https://monarchinitiative.org/MONDO:0010188"
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    "mondo_id": "MONDO:0010735",
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    "mondo_label_ja": "ケネディ病",
    "mondo_label_en": "Kennedy disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0010735"
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    "nando_id": "NANDO:1200062",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200062",
    "mondo_id": "MONDO:0011871",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "ニーマン・ピック病B型",
    "mondo_label_en": "Niemann-Pick disease type B",
    "mondo_url": "https://monarchinitiative.org/MONDO:0011871"
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    "nando_id": "NANDO:1200048",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200048",
    "mondo_id": "MONDO:0013594",
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    "mondo_label_ja": "脊髄小脳失調症36型",
    "mondo_label_en": "spinocerebellar ataxia type 36",
    "mondo_url": "https://monarchinitiative.org/MONDO:0013594"
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    "nando_id": "NANDO:1200053",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200053",
    "mondo_id": "MONDO:0015149",
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    "mondo_label_ja": "純粋型遺伝性痙性対麻痺",
    "mondo_label_en": "pure hereditary spastic paraplegia",
    "mondo_url": "https://monarchinitiative.org/MONDO:0015149"
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    "nando_id": "NANDO:1200054",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200054",
    "mondo_id": "MONDO:0015150",
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    "mondo_label_ja": "複合型遺伝性痙性対麻痺",
    "mondo_label_en": "complex hereditary spastic paraplegia",
    "mondo_url": "https://monarchinitiative.org/MONDO:0015150"
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    "nando_id": "NANDO:1200016",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200016",
    "mondo_id": "MONDO:0015626",
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    "mondo_label_ja": "シャルコー・マリー・トゥース病",
    "mondo_label_en": "Charcot-Marie-Tooth disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0015626"
  },
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    "nando_id": "NANDO:1200075",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200075",
    "mondo_id": "MONDO:0016089",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "乳児型クラッベ病",
    "mondo_label_en": "infantile Krabbe disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016089"
  },
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    "nando_id": "NANDO:1200077",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200077",
    "mondo_id": "MONDO:0016091",
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    "mondo_label_ja": "成人型クラッベ病",
    "mondo_label_en": "adult Krabbe disease",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016091"
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    "nando_id": "NANDO:1200001",
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    "mondo_id": "MONDO:0016113",
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    "mondo_label_ja": "球脊髄性筋萎縮症",
    "mondo_label_en": "bulbospinal muscular atrophy",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016113"
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    "nando_id": "NANDO:1200065",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200065",
    "mondo_id": "MONDO:0016310",
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    "mondo_label_ja": "ニーマン・ピック病C型, 成人期神経発症",
    "mondo_label_en": "Niemann-Pick disease type C, adult neurologic onset",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016310"
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    "nando_id": "NANDO:1200035",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200035",
    "mondo_id": "MONDO:0016418",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "MSA-C",
    "mondo_label_en": "multiple system atrophy, cerebellar type",
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    "nando_id": "NANDO:1200028",
    "nando_uid": "http://nanbyodata.jp/ontology/NANDO_1200028",
    "mondo_id": "MONDO:0016430",
    "property": "http://www.w3.org/2004/02/skos/core#exactMatch",
    "mondo_label_ja": "Baló病",
    "mondo_label_en": "Balo concentric sclerosis",
    "mondo_url": "https://monarchinitiative.org/MONDO:0016430"
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    "mondo_id": "MONDO:0004691",
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    "mondo_label_ja": "デニス・ドラッシュ症候群",
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    "mondo_id": "MONDO:0008977",
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    "mondo_label_ja": "軟骨肉腫",
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    "mondo_label_ja": "ファイファー症候群",
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    "mondo_id": "MONDO:0007113",
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    "mondo_label_ja": "アンジェルマン症候群",
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    "mondo_label_ja": "アラジール症候群",
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    "mondo_label_ja": "ネコ鳴き症候群",
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    "mondo_label_ja": "マルファン症候群",
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    "mondo_id": "MONDO:0016601",
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    "mondo_id": "MONDO:0009756",
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