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    "id": "NANDO:1200010",
    "uid": "http://nanbyodata.jp/ontology/NANDO_1200010",
    "type": "parent"
  },
  {
    "parent": "NANDO:1200010",
    "id": "H00057",
    "displayid": "H00057",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "パーキンソン病",
    "kegg_label_en": "Parkinson disease",
    "kegg_url": "https://identifiers.org/kegg.disease:H00057"
  },
  {
    "id": "NANDO:1200012",
    "uid": "http://nanbyodata.jp/ontology/NANDO_1200012",
    "type": "parent"
  },
  {
    "parent": "NANDO:1200012",
    "id": "H00059",
    "displayid": "H00059",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "ハンチントン病",
    "kegg_label_en": "Huntington disease",
    "kegg_url": "https://identifiers.org/kegg.disease:H00059"
  },
  {
    "id": "NANDO:1200009",
    "uid": "http://nanbyodata.jp/ontology/NANDO_1200009",
    "type": "parent"
  },
  {
    "parent": "NANDO:1200009",
    "id": "H00077",
    "displayid": "H00077",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "進行性核上性麻痺",
    "kegg_label_en": "Progressive supranuclear palsy",
    "kegg_url": "https://identifiers.org/kegg.disease:H00077"
  },
  {
    "parent": "NANDO:1200009",
    "id": "H00077",
    "displayid": "H00077",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "進行性核上性麻痺",
    "kegg_label_en": "Steele-Richardson-Olszewski syndrome",
    "kegg_url": "https://identifiers.org/kegg.disease:H00077"
  },
  {
    "id": "NANDO:1200157",
    "uid": "http://nanbyodata.jp/ontology/NANDO_1200157",
    "type": "parent"
  },
  {
    "parent": "NANDO:1200157",
    "id": "H00125",
    "displayid": "H00125",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "ファブリー病",
    "kegg_label_en": "Fabry disease",
    "kegg_url": "https://identifiers.org/kegg.disease:H00125"
  },
  {
    "parent": "NANDO:1200157",
    "id": "H00125",
    "displayid": "H00125",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "ファブリー病",
    "kegg_label_en": "Anderson-Fabry disease",
    "kegg_url": "https://identifiers.org/kegg.disease:H00125"
  },
  {
    "id": "NANDO:1200056",
    "uid": "http://nanbyodata.jp/ontology/NANDO_1200056",
    "type": "parent"
  },
  {
    "parent": "NANDO:1200056",
    "id": "H00126",
    "displayid": "H00126",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "ゴーシェ病",
    "kegg_label_en": "Gaucher disease",
    "kegg_url": "https://identifiers.org/kegg.disease:H00126"
  },
  {
    "id": "NANDO:1200078",
    "uid": "http://nanbyodata.jp/ontology/NANDO_1200078",
    "type": "parent"
  },
  {
    "parent": "NANDO:1200078",
    "id": "H00127",
    "displayid": "H00127",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "異染性白質ジストロフィー",
    "kegg_label_en": "Metachromatic leukodystrophy",
    "kegg_url": "https://identifiers.org/kegg.disease:H00127"
  },
  {
    "id": "NANDO:1200097",
    "uid": "http://nanbyodata.jp/ontology/NANDO_1200097",
    "type": "parent"
  },
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    "parent": "NANDO:1200097",
    "id": "H00129",
    "displayid": "H00129",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "ハンター症候群",
    "kegg_label_en": "Hunter syndrome",
    "kegg_url": "https://identifiers.org/kegg.disease:H00129"
  },
  {
    "parent": "NANDO:1200097",
    "id": "H00129",
    "displayid": "H00129",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "ムコ多糖症 II 型",
    "kegg_label_en": "Hunter syndrome",
    "kegg_url": "https://identifiers.org/kegg.disease:H00129"
  },
  {
    "parent": "NANDO:1200097",
    "id": "H00129",
    "displayid": "H00129",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "ハンター症候群",
    "kegg_label_en": "Mucopolysaccharidosis type II",
    "kegg_url": "https://identifiers.org/kegg.disease:H00129"
  },
  {
    "parent": "NANDO:1200097",
    "id": "H00129",
    "displayid": "H00129",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "ムコ多糖症 II 型",
    "kegg_label_en": "Mucopolysaccharidosis type II",
    "kegg_url": "https://identifiers.org/kegg.disease:H00129"
  },
  {
    "id": "NANDO:1200108",
    "uid": "http://nanbyodata.jp/ontology/NANDO_1200108",
    "type": "parent"
  },
  {
    "parent": "NANDO:1200108",
    "id": "H00131",
    "displayid": "H00131",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "マロトー・ラミー症候群",
    "kegg_label_en": "Maroteaux-Lamy syndrome",
    "kegg_url": "https://identifiers.org/kegg.disease:H00131"
  },
  {
    "parent": "NANDO:1200108",
    "id": "H00131",
    "displayid": "H00131",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "ムコ多糖症 VI 型",
    "kegg_label_en": "Maroteaux-Lamy syndrome",
    "kegg_url": "https://identifiers.org/kegg.disease:H00131"
  },
  {
    "parent": "NANDO:1200108",
    "id": "H00131",
    "displayid": "H00131",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "マロトー・ラミー症候群",
    "kegg_label_en": "Mucopolysaccharidosis type VI",
    "kegg_url": "https://identifiers.org/kegg.disease:H00131"
  },
  {
    "parent": "NANDO:1200108",
    "id": "H00131",
    "displayid": "H00131",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "ムコ多糖症 VI 型",
    "kegg_label_en": "Mucopolysaccharidosis type VI",
    "kegg_url": "https://identifiers.org/kegg.disease:H00131"
  },
  {
    "id": "NANDO:1200111",
    "uid": "http://nanbyodata.jp/ontology/NANDO_1200111",
    "type": "parent"
  },
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    "parent": "NANDO:1200111",
    "id": "H00132",
    "displayid": "H00132",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "スライ症候群",
    "kegg_label_en": "Mucopolysaccharidosis type VII",
    "kegg_url": "https://identifiers.org/kegg.disease:H00132"
  },
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    "parent": "NANDO:1200111",
    "id": "H00132",
    "displayid": "H00132",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "ムコ多糖症 VII 型",
    "kegg_label_en": "Mucopolysaccharidosis type VII",
    "kegg_url": "https://identifiers.org/kegg.disease:H00132"
  },
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    "parent": "NANDO:1200111",
    "id": "H00132",
    "displayid": "H00132",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "スライ症候群",
    "kegg_label_en": "Sly syndrome",
    "kegg_url": "https://identifiers.org/kegg.disease:H00132"
  },
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    "parent": "NANDO:1200111",
    "id": "H00132",
    "displayid": "H00132",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "ムコ多糖症 VII 型",
    "kegg_label_en": "Sly syndrome",
    "kegg_url": "https://identifiers.org/kegg.disease:H00132"
  },
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    "id": "NANDO:1200115",
    "uid": "http://nanbyodata.jp/ontology/NANDO_1200115",
    "type": "parent"
  },
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    "parent": "NANDO:1200115",
    "id": "H00133",
    "displayid": "H00133",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "ヒアルロニダーゼ欠損症",
    "kegg_label_en": "Hyaluronidase deficiency",
    "kegg_url": "https://identifiers.org/kegg.disease:H00133"
  },
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    "parent": "NANDO:1200115",
    "id": "H00133",
    "displayid": "H00133",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "ムコ多糖症 IX 型",
    "kegg_label_en": "Hyaluronidase deficiency",
    "kegg_url": "https://identifiers.org/kegg.disease:H00133"
  },
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    "parent": "NANDO:1200115",
    "id": "H00133",
    "displayid": "H00133",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "ヒアルロニダーゼ欠損症",
    "kegg_label_en": "Mucopolysaccharidosis type IX",
    "kegg_url": "https://identifiers.org/kegg.disease:H00133"
  },
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    "parent": "NANDO:1200115",
    "id": "H00133",
    "displayid": "H00133",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "ムコ多糖症 IX 型",
    "kegg_label_en": "Mucopolysaccharidosis type IX",
    "kegg_url": "https://identifiers.org/kegg.disease:H00133"
  },
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    "id": "NANDO:1200074",
    "uid": "http://nanbyodata.jp/ontology/NANDO_1200074",
    "type": "parent"
  },
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    "parent": "NANDO:1200074",
    "id": "H00135",
    "displayid": "H00135",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "クラッベ病",
    "kegg_label_en": "Krabbe disease",
    "kegg_url": "https://identifiers.org/kegg.disease:H00135"
  },
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    "parent": "NANDO:1200074",
    "id": "H00135",
    "displayid": "H00135",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "グロボイド細胞白質ジストロフィー",
    "kegg_label_en": "Krabbe disease",
    "kegg_url": "https://identifiers.org/kegg.disease:H00135"
  },
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    "parent": "NANDO:1200074",
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    "displayid": "H00135",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "クラッベ病",
    "kegg_label_en": "Globoid cell leukodystrophy",
    "kegg_url": "https://identifiers.org/kegg.disease:H00135"
  },
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    "parent": "NANDO:1200074",
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    "displayid": "H00135",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "グロボイド細胞白質ジストロフィー",
    "kegg_label_en": "Globoid cell leukodystrophy",
    "kegg_url": "https://identifiers.org/kegg.disease:H00135"
  },
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    "id": "NANDO:1200063",
    "uid": "http://nanbyodata.jp/ontology/NANDO_1200063",
    "type": "parent"
  },
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    "parent": "NANDO:1200063",
    "id": "H00136",
    "displayid": "H00136",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "ニーマン・ピック病 C 型",
    "kegg_label_en": "Niemann-Pick disease type C",
    "kegg_url": "https://identifiers.org/kegg.disease:H00136"
  },
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    "id": "NANDO:1200086",
    "uid": "http://nanbyodata.jp/ontology/NANDO_1200086",
    "type": "parent"
  },
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    "parent": "NANDO:1200086",
    "id": "H00138",
    "displayid": "H00138",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "ファーバー病",
    "kegg_label_en": "Farber disease",
    "kegg_url": "https://identifiers.org/kegg.disease:H00138"
  },
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    "parent": "NANDO:1200086",
    "id": "H00138",
    "displayid": "H00138",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "ファーバー脂肪性肉芽腫症",
    "kegg_label_en": "Farber disease",
    "kegg_url": "https://identifiers.org/kegg.disease:H00138"
  },
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    "parent": "NANDO:1200086",
    "id": "H00138",
    "displayid": "H00138",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "ファーバー病",
    "kegg_label_en": "Farber lipogranulomatosis",
    "kegg_url": "https://identifiers.org/kegg.disease:H00138"
  },
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    "parent": "NANDO:1200086",
    "id": "H00138",
    "displayid": "H00138",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "ファーバー脂肪性肉芽腫症",
    "kegg_label_en": "Farber lipogranulomatosis",
    "kegg_url": "https://identifiers.org/kegg.disease:H00138"
  },
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    "id": "NANDO:1200126",
    "uid": "http://nanbyodata.jp/ontology/NANDO_1200126",
    "type": "parent"
  },
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    "parent": "NANDO:1200126",
    "id": "H00139",
    "displayid": "H00139",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "α-マンノシドーシス",
    "kegg_label_en": "alpha-Mannosidosis",
    "kegg_url": "https://identifiers.org/kegg.disease:H00139"
  },
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    "id": "NANDO:1200129",
    "uid": "http://nanbyodata.jp/ontology/NANDO_1200129",
    "type": "parent"
  },
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    "parent": "NANDO:1200129",
    "id": "H00140",
    "displayid": "H00140",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "β-マンノシドーシス",
    "kegg_label_en": "beta-Mannosidosis",
    "kegg_url": "https://identifiers.org/kegg.disease:H00140"
  },
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    "id": "NANDO:1200116",
    "uid": "http://nanbyodata.jp/ontology/NANDO_1200116",
    "type": "parent"
  },
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    "parent": "NANDO:1200116",
    "id": "H00142",
    "displayid": "H00142",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "シアリドーシス",
    "kegg_label_en": "Sialidosis",
    "kegg_url": "https://identifiers.org/kegg.disease:H00142"
  },
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    "parent": "NANDO:1200116",
    "id": "H00142",
    "displayid": "H00142",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "ムコリピドーシス 1 型",
    "kegg_label_en": "Sialidosis",
    "kegg_url": "https://identifiers.org/kegg.disease:H00142"
  },
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    "parent": "NANDO:1200116",
    "id": "H00142",
    "displayid": "H00142",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "シアリドーシス",
    "kegg_label_en": "Mucolipidosis I",
    "kegg_url": "https://identifiers.org/kegg.disease:H00142"
  },
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    "parent": "NANDO:1200116",
    "id": "H00142",
    "displayid": "H00142",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "ムコリピドーシス 1 型",
    "kegg_label_en": "Mucolipidosis I",
    "kegg_url": "https://identifiers.org/kegg.disease:H00142"
  },
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    "id": "NANDO:1200124",
    "uid": "http://nanbyodata.jp/ontology/NANDO_1200124",
    "type": "parent"
  },
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    "parent": "NANDO:1200124",
    "id": "H00143",
    "displayid": "H00143",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "I 細胞病",
    "kegg_label_en": "I-cell disease",
    "kegg_url": "https://identifiers.org/kegg.disease:H00143"
  },
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    "parent": "NANDO:1200124",
    "id": "H00143",
    "displayid": "H00143",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "ムコリピドーシス II 型",
    "kegg_label_en": "I-cell disease",
    "kegg_url": "https://identifiers.org/kegg.disease:H00143"
  },
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    "parent": "NANDO:1200124",
    "id": "H00143",
    "displayid": "H00143",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "I 細胞病",
    "kegg_label_en": "Mucolipidosis II",
    "kegg_url": "https://identifiers.org/kegg.disease:H00143"
  },
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    "parent": "NANDO:1200124",
    "id": "H00143",
    "displayid": "H00143",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "ムコリピドーシス II 型",
    "kegg_label_en": "Mucolipidosis II",
    "kegg_url": "https://identifiers.org/kegg.disease:H00143"
  },
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    "id": "NANDO:1200133",
    "uid": "http://nanbyodata.jp/ontology/NANDO_1200133",
    "type": "parent"
  },
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    "parent": "NANDO:1200133",
    "id": "H00145",
    "displayid": "H00145",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "アスパルチルグルコサミン尿症",
    "kegg_label_en": "Aspartylglucosaminuria",
    "kegg_url": "https://identifiers.org/kegg.disease:H00145"
  },
  {
    "id": "NANDO:1200165",
    "uid": "http://nanbyodata.jp/ontology/NANDO_1200165",
    "type": "parent"
  },
  {
    "parent": "NANDO:1200165",
    "id": "H00176",
    "displayid": "H00176",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "副腎白質ジストロフィー",
    "kegg_label_en": "Adrenoleukodystrophy",
    "kegg_url": "https://identifiers.org/kegg.disease:H00176"
  },
  {
    "id": "NANDO:1200016",
    "uid": "http://nanbyodata.jp/ontology/NANDO_1200016",
    "type": "parent"
  },
  {
    "parent": "NANDO:1200016",
    "id": "H00264",
    "displayid": "H00264",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "シャルコー・マリー・トゥース病",
    "kegg_label_en": "Charcot-Marie-Tooth disease",
    "kegg_url": "https://identifiers.org/kegg.disease:H00264"
  },
  {
    "parent": "NANDO:1200016",
    "id": "H00264",
    "displayid": "H00264",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "遺伝性運動感覚ニューロパチー",
    "kegg_label_en": "Charcot-Marie-Tooth disease",
    "kegg_url": "https://identifiers.org/kegg.disease:H00264"
  },
  {
    "parent": "NANDO:1200016",
    "id": "H00264",
    "displayid": "H00264",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "シャルコー・マリー・トゥース病",
    "kegg_label_en": "Hereditary motor and sensory neuropathy",
    "kegg_url": "https://identifiers.org/kegg.disease:H00264"
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    "displayid": "H01829",
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    "parent": "NANDO:1200597",
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    "displayid": "H01831",
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    "id": "NANDO:1200563",
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    "parent": "NANDO:1200563",
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    "displayid": "H01833",
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    "displayid": "H01835",
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    "parent": "NANDO:1200553",
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    "displayid": "H01836",
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    "displayid": "H00718",
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    "parent": "NANDO:1200614",
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    "id": "NANDO:1200645",
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    "parent": "NANDO:1200645",
    "id": "H00802",
    "displayid": "H00802",
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    "kegg_label_ja": "エーラス・ダンロス症候群",
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    "id": "NANDO:1200663",
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    "parent": "NANDO:1200663",
    "id": "H00908",
    "displayid": "H00908",
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    "kegg_label_ja": "モワットウィルソン症候群",
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    "id": "NANDO:1200670",
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    "parent": "NANDO:1200670",
    "id": "H01403",
    "displayid": "H01403",
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    "kegg_label_ja": "コフィン・シリス症候群",
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    "id": "NANDO:1200664",
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    "parent": "NANDO:1200664",
    "id": "H01439",
    "displayid": "H01439",
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    "kegg_label_ja": "ウィリアムズ症候群",
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    "id": "NANDO:1200632",
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    "parent": "NANDO:1200632",
    "id": "H01650",
    "displayid": "H01650",
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    "kegg_label_ja": "類天疱瘡",
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    "id": "NANDO:1200676",
    "uid": "http://nanbyodata.jp/ontology/NANDO_1200676",
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    "parent": "NANDO:1200676",
    "id": "H01733",
    "displayid": "H01733",
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    "id": "NANDO:1200671",
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    "parent": "NANDO:1200671",
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    "displayid": "H01734",
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    "displayid": "H01738",
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    "id": "NANDO:1200659",
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    "parent": "NANDO:1200659",
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    "displayid": "H01751",
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    "displayid": "H01753",
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    "displayid": "H00205",
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    "displayid": "H00217",
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    "displayid": "H00252",
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    "displayid": "H00533",
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    "parent": "NANDO:1200757",
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    "displayid": "H00916",
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    "displayid": "H01802",
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    "displayid": "H01803",
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    "displayid": "H00271",
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    "displayid": "H00292",
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    "displayid": "H00436",
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    "displayid": "H00454",
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    "displayid": "H01177",
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    "displayid": "H01388",
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    "displayid": "H01388",
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    "displayid": "H01396",
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    "displayid": "H01425",
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    "displayid": "H00183",
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    "displayid": "H00184",
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    "displayid": "H00186",
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    "displayid": "H00187",
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    "displayid": "H00189",
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    "parent": "NANDO:2200484",
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    "displayid": "H00190",
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    "id": "NANDO:2200476",
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    "displayid": "H00205",
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    "displayid": "H00210",
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    "kegg_label_ja": "無セルロプラスミン血症",
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  },
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    "kegg_label_ja": "セルロプラスミン欠損症",
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    "kegg_label_ja": "セルロプラスミン欠損症",
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    "kegg_url": "https://identifiers.org/kegg.disease:H02206"
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    "uid": "http://nanbyodata.jp/ontology/NANDO_1201154",
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    "displayid": "H00682",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "Woodhouse-Sakati 症候群",
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  },
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    "kegg_label_ja": "Woodhouse-Sakati 症候群",
    "kegg_label_en": "Hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome",
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  },
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    "id": "NANDO:1201153",
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    "type": "parent"
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    "id": "H02207",
    "displayid": "H02207",
    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "パーキンソン病 9 型",
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  },
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    "kegg_label_ja": "パーキンソン病 9 型",
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    "property": "http://www.geneontology.org/formats/oboInOwl#hasDbXref",
    "kegg_label_ja": "Kufor-Rakeb 症候群",
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  },
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    "kegg_label_ja": "Kufor-Rakeb 症候群",
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    "kegg_url": "https://identifiers.org/kegg.disease:H02207"
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]