{
  "id": 20799,
  "label": "Basaran Yilmaz syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0021979",
  "properties": {
    "xrefs": [
      "MEDGEN:419444",
      "MESH:C537660",
      "UMLS:C2931577"
    ],
    "synonyms": [
      "keratoderma, hypotrichosis and leukonychia totalis"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "A congenital hypotrichosis that is characterized by trichorrhexis nodosa and trichoptilosis, dry skin, keratosis pilaris and leukonychia totalis. Other features include progressive transgrediens type of palmoplantar keratoderma, and hyperkeratotic lesions on the knees, elbows and perianal region."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4897,
      "label": "nail disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4198
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:4123",
          "ICD9:703",
          "ICD9:703.8",
          "ICD9:703.9",
          "MEDGEN:10171",
          "MESH:D009260",
          "SCTID:17790008",
          "UMLS:C0027339"
        ],
        "synonyms": [
          "disease of nail",
          "disease or disorder of nail",
          "disorder of nail",
          "nail disease",
          "nail disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A disease involving the nail."
      },
      "child_count": 7,
      "reference_id": "MONDO:0002884"
    },
    {
      "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"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4897,
      "label": "nail disorder"
    },
    {
      "id": 5030,
      "label": "hypotrichosis"
    }
  ]
}