{
  "id": 9961,
  "label": "isolated familial wooly hair disorder",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008686",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 6,
  "parents": [
    {
      "id": 19134,
      "label": "hair anomaly",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4924,
        21436
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:539624",
          "Orphanet:79363",
          "UMLS:C0265991"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 16,
      "reference_id": "MONDO:0019278"
    }
  ],
  "children": [
    {
      "id": 11384,
      "label": "hypotrichosis 8",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        5030,
        9961,
        18841
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110705",
          "GARD:0015247",
          "MEDGEN:481100",
          "MESH:C566950",
          "OMIM:278150",
          "UMLS:C3279470"
        ],
        "synonyms": [
          "HYPT8",
          "LAH3",
          "LPAR6 hypotrichosis",
          "hypotrichosis 8",
          "hypotrichosis caused by mutation in LPAR6",
          "hypotrichosis type 8",
          "hypotrichosis, localized, autosomal recessive 3",
          "woolly hair, autosomal recessive 1, with or without hypotrichosis",
          "wooly hair, autosomal recessive 1, 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 LPAR6 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010206"
    },
    {
      "id": 12556,
      "label": "hypotrichosis 7",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        5030,
        9961,
        18841
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011452"
    },
    {
      "id": 15392,
      "label": "hypotrichosis 13",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        5030,
        9961
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0110710",
          "GARD:0016029",
          "MEDGEN:863053",
          "OMIM:615896",
          "UMLS:C4014616"
        ],
        "synonyms": [
          "HYPT13",
          "KRT71 hypotrichosis",
          "hypotrichosis 13",
          "hypotrichosis caused by mutation in KRT71",
          "hypotrichosis type 13",
          "hypotrichosis with woolly hair",
          "hypotrichosis with wooly hair",
          "hypt13"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Any hypotrichosis in which the cause of the disease is a mutation in the KRT71 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014390"
    },
    {
      "id": 15754,
      "label": "wooly hair, autosomal recessive 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        5714,
        9961
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0014765"
    },
    {
      "id": 20124,
      "label": "autosomal dominant wooly hair",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        5714,
        9961
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111573",
          "GARD:0025222",
          "MEDGEN:348571",
          "OMIM:194300",
          "UMLS:C1860238"
        ],
        "synonyms": [
          "woolly hair, autosomal dominant",
          "wooly hair, autosomal dominant",
          "ADWH"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0020717"
    },
    {
      "id": 24915,
      "label": "wooly hair, autosomal recessive 1, with or without hypotrichosis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9961
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026495",
          "MEDGEN:341227",
          "UMLS:C1848435"
        ],
        "synonyms": [
          "ARWH1"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0800312"
    }
  ],
  "roots": [
    {
      "id": 19134,
      "label": "hair anomaly"
    }
  ]
}