{
  "id": 14544,
  "label": "hypotrichosis 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013514",
  "properties": {
    "xrefs": [
      "DOID:0110700",
      "GARD:0018094",
      "MEDGEN:462782",
      "OMIM:613981",
      "UMLS:C3151432"
    ],
    "synonyms": [
      "HTSS2",
      "HYPT3",
      "Htss2",
      "KRT74 hypotrichosis",
      "hypotrichosis 3",
      "hypotrichosis caused by mutation in KRT74",
      "hypotrichosis simplex of the scalp 2",
      "hypotrichosis type 3",
      "hypt3"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "Any hypotrichosis in which the cause of the disease is a mutation in the KRT74 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 5030,
      "label": "hypotrichosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4924,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:4535",
          "ICD9:704.09",
          "MEDGEN:6993",
          "MESH:D007039",
          "NCIT:C34720",
          "OMIMPS:605389",
          "SCTID:53602002",
          "UMLS:C0020678"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A congenital condition, usually due to genetic aberrations, that is characterized by a lack of hair growth on the head and/or body."
      },
      "child_count": 38,
      "reference_id": "MONDO:0003037"
    },
    {
      "id": 19380,
      "label": "hypotrichosis simplex of the scalp",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6660
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016789",
          "Orphanet:90368",
          "SCTID:717256009"
        ],
        "synonyms": [
          "hereditary hypotrichosis simplex of the scalp"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Hypotrichosis simplex of the scalp (HSS) is characterized by diffuse progressive hair loss that is confined to the scalp."
      },
      "child_count": 2,
      "reference_id": "MONDO:0019575"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5030,
      "label": "hypotrichosis"
    },
    {
      "id": 19380,
      "label": "hypotrichosis simplex of the scalp"
    }
  ]
}