{
  "id": 11899,
  "label": "Wildervanck syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010759",
  "properties": {
    "xrefs": [
      "GARD:0005569",
      "ICD9:759.89",
      "MEDGEN:120518",
      "MedDRA:10069402",
      "NORD:1853",
      "OMIM:314600",
      "Orphanet:3456",
      "SCTID:79665007",
      "UMLS:C0265239"
    ],
    "synonyms": [
      "Cervicooculoacoustic syndrome",
      "Wildervanck syndrome",
      "COA syndrome",
      "cervico-oculo-acoustic dysplasia",
      "cervico-oculo-acoustic syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Wildervanck syndrome is characterized by the triad of cervical vertebral fusion (Klippel-Feil anomaly), bilateral abducens palsy with retracted eyes (Duane syndrome) and congenital perceptive deafness."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3287,
      "label": "Klippel-Feil syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4222,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:10426",
          "GARD:0010280",
          "ICD10CM:Q76.1",
          "ICD9:756.16",
          "MEDGEN:9645",
          "MESH:D007714",
          "NCIT:C98967",
          "OMIMPS:118100",
          "Orphanet:2345",
          "SCTID:5601008",
          "UMLS:C0022738",
          "icd11.foundation:2139186992"
        ],
        "synonyms": [
          "Klippel-Feil Sequence",
          "Klippel Feil syndrome",
          "Klippel-Feil and Turner syndrome",
          "Klippel-Feil deformity, deafness and facial asymmetry",
          "autosomal dominant Klippel-Feil syndrome",
          "cervical vertebral fusion",
          "congenital dystrophia brevicollis",
          "congenital synostosis of cervical vertebrae"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A congenital, musculoskeletal condition characterized by the fusion of at least two vertebrae of the neck. Common symptoms include a short neck, low hairline at the back of the head, and restricted mobility of the upper spine. This syndrome can cause chronic headaches as well as pain in both the neck and the back.Other features may involve various other body parts or systems. Sometimes, KFS occurs as a feature of another disorder or syndrome, such as Wildervanck syndrome or hemifacial microsomia. In these cases, people have the features of both KFS and the additional disorder. KFS may be caused by mutations in the GDF6 or GDF3 gene and inherited in an autosomal dominant manner; or, it may be caused by mutations in the MEOX1 gene and inherited in an autosomal recessive manner. Treatment is symptomatic and may include medications, surgery, and/or physical therapy."
      },
      "child_count": 12,
      "reference_id": "MONDO:0001029"
    },
    {
      "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"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3287,
      "label": "Klippel-Feil syndrome"
    },
    {
      "id": 4370,
      "label": "syndromic disease"
    }
  ]
}