{
  "id": 9963,
  "label": "WT limb-blood syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008688",
  "properties": {
    "xrefs": [
      "GARD:0000039",
      "MEDGEN:231231",
      "MESH:C536751",
      "OMIM:194350",
      "Orphanet:3466",
      "SCTID:719019000",
      "UMLS:C1327917",
      "icd11.foundation:1407849410"
    ],
    "synonyms": [
      "WT limb-blood syndrome",
      "WT limb blood syndrome",
      "WTsyndrome",
      "radial-ulnar hypoplasia with bone marrow failure and/or leukaemia",
      "radial-ulnar hypoplasia with bone marrow failure and/or leukemia"
    ],
    "categories": [
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "WT limb-blood syndrome is characterized by hematological anomalies (Fanconi anemia, leukemia and lymphoma) often appearing during childhood. Anomalies of the limbs and hands are also present: bifid or hypoplastic thumbs, cutaneous syndactyly, and ulnar and radial defects. The syndrome has been described in several families. Transmission is autosomal dominant."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3901,
      "label": "inherited aplastic anemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        16610
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1342",
          "GARD:0018889",
          "ICD10CM:D61.0",
          "ICD9:284.0",
          "ICD9:284.09",
          "MEDGEN:1826154",
          "MESH:D029502",
          "NANDO:1200302",
          "NANDO:2201275",
          "Orphanet:397692",
          "Orphanet:68383",
          "SCTID:28975000",
          "UMLS:C5681331"
        ],
        "synonyms": [
          "constitutional aplastic anaemia",
          "constitutional aplastic anemia",
          "hereditary aplastic anaemia",
          "hereditary aplastic anemia",
          "rare constitutional aplastic anaemia",
          "rare constitutional aplastic anemia",
          "congenital aplastic anaemia",
          "congenital aplastic anemia",
          "congenital hypoplastic anaemia",
          "congenital hypoplastic anemia",
          "hypoplastic anaemia - familial",
          "hypoplastic anemia - familial"
        ],
        "categories": [
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "An inborn condition characterized by deficiencies of red cell precursors that sometimes also includes leukopenia and thrombocytopenia."
      },
      "child_count": 10,
      "reference_id": "MONDO:0001713"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3901,
      "label": "inherited aplastic anemia"
    }
  ]
}