{
  "id": 19380,
  "label": "hypotrichosis simplex of the scalp",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0019575",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 6660,
      "label": "alopecia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19134
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:987",
          "ICD9:704.0",
          "ICD9:704.00",
          "ICD9:704.09",
          "MEDGEN:7982",
          "MESH:D000505",
          "NCIT:C50575",
          "Orphanet:79364",
          "SCTID:56317004",
          "UMLS:C0002170",
          "icd11.foundation:1313926062"
        ],
        "synonyms": [
          "alopecia",
          "hair loss",
          "loss Of hair",
          "alopecia areata"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Hair loss usually from the scalp. It may result in bald spots or spread to the entire scalp or the entire epidermis. It may be androgenetic or caused by chemotherapeutic agents, compulsive hair pulling, autoimmune disorders or congenital conditions."
      },
      "child_count": 26,
      "reference_id": "MONDO:0004907"
    }
  ],
  "children": [
    {
      "id": 9148,
      "label": "hypotrichosis 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        5030,
        19380
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110699",
          "GARD:0018093",
          "MEDGEN:374435",
          "MESH:C564143",
          "OMIM:146520",
          "UMLS:C1840299"
        ],
        "synonyms": [
          "CDSN hypotrichosis",
          "HYPT2",
          "hypotrichosis 2",
          "hypotrichosis caused by mutation in CDSN",
          "hypotrichosis simplex of the scalp 1",
          "hypotrichosis type 2",
          "hypt2",
          "Htss",
          "hypotrichosis, Spanish type"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Any hypotrichosis in which the cause of the disease is a mutation in the CDSN gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007805"
    },
    {
      "id": 14544,
      "label": "hypotrichosis 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        5030,
        19380
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013514"
    }
  ],
  "roots": [
    {
      "id": 6660,
      "label": "alopecia"
    }
  ]
}