{
  "id": 11385,
  "label": "wooly hair-hypotrichosis-everted lower lip-outstanding ears syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010207",
  "properties": {
    "xrefs": [
      "GARD:0005594",
      "MEDGEN:98033",
      "MESH:C536746",
      "OMIM:278200",
      "Orphanet:1409",
      "SCTID:239023005",
      "UMLS:C0406718"
    ],
    "synonyms": [
      "Salamon syndrome",
      "wooly hair-hypotrichosis-everted lower lip-outstanding ears syndrome",
      "woolly hair hypotrichosis everted lower lip and outstanding ears",
      "woolly hair, hypotrichosis, everted LOWER LIP, and outstanding ears",
      "wooly hair hypotrichosis everted lower lip and outstanding ears",
      "wooly hair, hypotrichosis, everted LOWER LIP, and outstanding ears"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ]
  },
  "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"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    }
  ]
}