{
  "id": 15037,
  "label": "hypotrichosis 11",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014027",
  "properties": {
    "xrefs": [
      "DOID:0110708",
      "GARD:0015900",
      "MEDGEN:767323",
      "OMIM:615059",
      "UMLS:C3554409"
    ],
    "synonyms": [
      "HYPT11",
      "SNRPE hypotrichosis",
      "hypotrichosis 11",
      "hypotrichosis caused by mutation in SNRPE",
      "hypotrichosis type 11",
      "hypt11"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "Any hypotrichosis in which the cause of the disease is a mutation in the SNRPE 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": 18841,
      "label": "hypotrichosis simplex",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6660
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0009170",
          "MEDGEN:344257",
          "MESH:C537160",
          "Orphanet:55654",
          "SCTID:723362004",
          "UMLS:C1854310"
        ],
        "synonyms": [
          "hereditary hypotrichosis simplex"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Hypotrichosis simplex (HS) or hereditary hypotrichosis simplex (HHS) is characterized by reduced pilosity over the scalp and body (with sparse, thin, and short hair) in the absence of other anomalies."
      },
      "child_count": 8,
      "reference_id": "MONDO:0018914"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 5030,
      "label": "hypotrichosis"
    },
    {
      "id": 18841,
      "label": "hypotrichosis simplex"
    }
  ]
}