{
  "id": 21093,
  "label": "Drachtman Weinblatt Sitarz syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0023007",
  "properties": {
    "xrefs": [
      "GARD:0001913",
      "MEDGEN:419292",
      "MESH:C535603",
      "UMLS:C2930947"
    ],
    "synonyms": [
      "Drachtman Weinblatt Sitarz syndrome",
      "marrow hypoplasia associated with congenital neurologic anomalies"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      },
      {
        "ref": "MONDO:0005570",
        "name": "hematologic disorder"
      }
    ],
    "definition": "A rare genetic disorder, characterized by under-development of bone marrow and neurological disorders such as weakness on one side of the body, agenesis of corpus callosum and hydrocephalus."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4370,
      "label": "syndromic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:225",
          "MEDGEN:11688",
          "MESH:D013577",
          "NCIT:C28193",
          "OGMS:0000086",
          "UMLS:C0039082"
        ],
        "synonyms": [
          "cluster, symptom",
          "clusters, symptom",
          "symptom cluster",
          "symptom clusters",
          "syndrome",
          "syndrome associated with disease or disorder",
          "syndromes",
          "syndromic disease",
          "syndromic disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition."
      },
      "child_count": 1182,
      "reference_id": "MONDO:0002254"
    },
    {
      "id": 5177,
      "label": "bone marrow disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6778,
        6893,
        7217
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:4961",
          "GARD:0023414",
          "ICD9:289.9",
          "MEDGEN:892905",
          "MESH:D001855",
          "NCIT:C34433",
          "SCTID:127035006",
          "UMLS:C4021634"
        ],
        "synonyms": [
          "bone marrow disease",
          "bone marrow disease or disorder",
          "bone marrow disorder",
          "disease of bone marrow",
          "disease or disorder of bone marrow",
          "disorder of bone marrow"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "Any disease of the bone marrow."
      },
      "child_count": 21,
      "reference_id": "MONDO:0003225"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 5177,
      "label": "bone marrow disorder"
    }
  ]
}