{
  "id": 11898,
  "label": "Wieacker-Wolff syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010758",
  "properties": {
    "xrefs": [
      "DOID:0060815",
      "GARD:0007890",
      "MEDGEN:163227",
      "MESH:C536703",
      "MESH:C537472",
      "NORD:91159",
      "OMIM:314580",
      "Orphanet:3454",
      "Orphanet:85283",
      "SCTID:719012009",
      "SCTID:722456001",
      "UMLS:C0796200"
    ],
    "synonyms": [
      "MCS",
      "MRXS4",
      "Miles-CARPENTER X-linked mental retardation syndrome",
      "Miles-Carpenter syndrome",
      "WRWF",
      "WRWFXLR",
      "Wieacker Wolff syndrome",
      "Wieacker syndrome",
      "Wieacker-Wolff syndrome",
      "Wieacker-Wolff syndrome, X-linked",
      "Wieacker-Wolff syndrome, X-linked recessive",
      "X-linked intellectual disability, Miles-Carpenter type",
      "ZC4H2-Associated Rare Disorders (ZARD)",
      "apraxia, oculomotor, with congenital contractures and muscle atrophy",
      "contractures of feet, muscle atrophy, and oculomotor apraxia",
      "foot contractures-muscle atrophy-oculomotor apraxia syndrome",
      "intellectual disability-developmental delay-contractures syndrome",
      "mental retardation, X-linked, syndromic 4",
      "mental retardation, X-linked, with congenital contractures and Low fingertip arches",
      "mental retardation, X-linked, with congenital contractures and low fingertip arches"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A severe X-linked recessive neurodevelopmental disorder characterized by severe contractures (arthrogryposis) and intellectual disability."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4427,
      "label": "congenital nervous system disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2490",
          "ICD9:742",
          "MEDGEN:105425",
          "NCIT:C97172",
          "UMLS:C0497552"
        ],
        "synonyms": [
          "congenital abnormality of the nervous system",
          "congenital nervous system disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An abnormality of the nervous system that is present at birth or detected in the neonatal period."
      },
      "child_count": 217,
      "reference_id": "MONDO:0002320"
    },
    {
      "id": 21691,
      "label": "Wieacker-Wolff syndrome (spectrum)",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16094,
        24618
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025477",
          "OMIMPS:314580"
        ],
        "synonyms": [
          "ZARD",
          "ZC4H2-associated disorder",
          "ZC4H2-associated rare disorders"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 4,
      "reference_id": "MONDO:0025445"
    },
    {
      "id": 24226,
      "label": "Mendelian neurodevelopmental disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24270,
        24488
      ],
      "type_id": 0,
      "properties": {
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A neurodevelopmental disorder that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 550,
      "reference_id": "MONDO:0100500"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4427,
      "label": "congenital nervous system disorder"
    },
    {
      "id": 21691,
      "label": "Wieacker-Wolff syndrome (spectrum)"
    },
    {
      "id": 24226,
      "label": "Mendelian neurodevelopmental disorder"
    }
  ]
}