{
  "id": 20124,
  "label": "autosomal dominant wooly hair",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0020717",
  "properties": {
    "xrefs": [
      "DOID:0111573",
      "GARD:0025222",
      "MEDGEN:348571",
      "OMIM:194300",
      "UMLS:C1860238"
    ],
    "synonyms": [
      "woolly hair, autosomal dominant",
      "wooly hair, autosomal dominant",
      "ADWH"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    },
    {
      "id": 9961,
      "label": "isolated familial wooly hair disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19134
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111572",
          "GARD:0005597",
          "HP:0002224",
          "MEDGEN:87469",
          "MESH:C536745",
          "MedDRA:10048017",
          "Orphanet:170",
          "SCTID:52564001",
          "UMLS:C0343073"
        ],
        "synonyms": [
          "familial woolly hair syndrome",
          "familial wooly hair syndrome",
          "hereditary woolly hair syndrome",
          "hereditary wooly hair syndrome",
          "woolly hair",
          "wooly hair",
          "ADWH",
          "familial woolly hair (autosomal recessive)",
          "familial wooly hair (autosomal recessive)",
          "hereditary woolly hair (autosomal dominant)",
          "hereditary wooly hair (autosomal dominant)",
          "woolly hair syndrome",
          "woolly hair, autosomal dominant",
          "wooly hair syndrome",
          "wooly hair, autosomal dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Woolly hair is a rare congenital abnormality of the structure of the scalp hair marked by extreme kinkiness of the hair."
      },
      "child_count": 6,
      "reference_id": "MONDO:0008686"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 9961,
      "label": "isolated familial wooly hair disorder"
    }
  ]
}