{
  "id": 15754,
  "label": "wooly hair, autosomal recessive 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014765",
  "properties": {
    "xrefs": [
      "DOID:0111574",
      "GARD:0016157",
      "MEDGEN:902275",
      "OMIM:616760",
      "UMLS:C4225214"
    ],
    "synonyms": [
      "ARWH3",
      "KRT25 woolly hair (disease)",
      "KRT25 wooly hair (disease)",
      "woolly hair (disease) caused by mutation in KRT25",
      "woolly hair, autosomal recessive type 3",
      "wooly hair (disease) caused by mutation in KRT25",
      "wooly hair, autosomal recessive 3",
      "wooly hair, autosomal recessive type 3",
      "woolly hair, autosomal recessive 3, with hypotrichosis",
      "wooly hair, autosomal recessive 3, with hypotrichosis"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "Any wooly hair in which the cause of the disease is a mutation in the KRT25 gene."
  },
  "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"
    }
  ]
}