{
  "id": 11690,
  "label": "Bazex-Dupre-Christol syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010535",
  "properties": {
    "xrefs": [
      "GARD:0000838",
      "ICD9:757.39",
      "MEDGEN:87539",
      "OMIM:301845",
      "Orphanet:113",
      "Orphanet:166113",
      "SCTID:238640007",
      "SCTID:254820002",
      "UMLS:C0346104"
    ],
    "synonyms": [
      "BDCS",
      "Bazex syndrome",
      "Bazex syndrome, X-linked dominant",
      "Bazex-Dupre-Christol syndrome",
      "Bazex-Dupré-Christol syndrome",
      "acrokeratosis of Bazex",
      "acrokeratosis paraneoplastica",
      "acrokeratosis paraneoplastica of Bazex",
      "follicular atrophoderma and basal cell carcinomas",
      "BZX",
      "follicular atrophoderma-basal cell carcinoma syndrome",
      "follicular atrophoderma-basocellular proliferations-hypotrichosis syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "Bazex-Dupre-Christol syndrome is a rare genodermatosis (hereditary skin disease) with a predisposition to early-onset basal cell carcinomas."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 6820,
      "label": "skin disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4198
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:37",
          "EFO:0000701",
          "ICD9:702",
          "ICD9:702.8",
          "ICD9:709.8",
          "MEDGEN:20777",
          "MESH:D012871",
          "NANDO:2100281",
          "NCIT:C3371",
          "SCTID:95320005",
          "UMLS:C0037274"
        ],
        "synonyms": [
          "cutaneous disorder",
          "disease of zone of skin",
          "disease or disorder of zone of skin",
          "disorder of skin",
          "disorder of zone of skin",
          "skin diseases and manifestations",
          "skin disorder",
          "zone of skin disease",
          "zone of skin disease or disorder",
          "dermatosis",
          "genodermatosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Any deviation from the normal structure or function of the skin or subcutaneous tissue that is manifested by a characteristic set of symptoms and signs."
      },
      "child_count": 72,
      "reference_id": "MONDO:0005093"
    }
  ],
  "children": [
    {
      "id": 19158,
      "label": "follicular atrophoderma-basal cell carcinoma",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        7027,
        11690
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025135",
          "Orphanet:79459"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0019317"
    }
  ],
  "roots": [
    {
      "id": 6820,
      "label": "skin disorder"
    }
  ]
}