{
  "id": 12556,
  "label": "hypotrichosis 7",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011452",
  "properties": {
    "xrefs": [
      "DOID:0110704",
      "GARD:0008178",
      "MEDGEN:322969",
      "MESH:C536973",
      "OMIM:604379",
      "UMLS:C1836672"
    ],
    "synonyms": [
      "HYPT7",
      "LAH2",
      "LIPH hypotrichosis",
      "Lah2",
      "hypotrichosis 7",
      "hypotrichosis caused by mutation in LIPH",
      "hypotrichosis type 7",
      "hypotrichosis, localized, autosomal recessive 2",
      "total Mari type hypotrichosis,",
      "woolly hair, autosomal recessive 2 with or without hypotrichosis",
      "wooly hair, autosomal recessive 2 with or without hypotrichosis",
      "Mari type alopecia universalis congenita",
      "Wh/Ht",
      "alopecia universalis congenita, Mari type",
      "hypotrichosis, autosomal recessive",
      "hypotrichosis, total, Mari type",
      "total hypotrichosis, Mari type",
      "woolly hair, autosomal recessive 2, with or without hypotrichosis",
      "wooly hair, autosomal recessive 2, with or without hypotrichosis"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "Any hypotrichosis in which the cause of the disease is a mutation in the LIPH 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": 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"
    },
    {
      "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": 9961,
      "label": "isolated familial wooly hair disorder"
    },
    {
      "id": 18841,
      "label": "hypotrichosis simplex"
    }
  ]
}