{
  "id": 11740,
  "label": "epidermodysplasia verruciformis, X-linked",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010587",
  "properties": {
    "xrefs": [
      "GARD:0015291",
      "MEDGEN:337033",
      "MESH:C564430",
      "OMIM:305350",
      "UMLS:C1844589"
    ],
    "synonyms": [
      "X-linked epidermodysplasia verruciformis",
      "epidermodysplasia verruciformis, X-linked",
      "EDV2",
      "EDVX"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      }
    ],
    "definition": "X-linked form of epidermodysplasia verruciformis."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2902,
      "label": "X-linked disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050735",
          "ICD9:799.89",
          "MEDGEN:222910",
          "MESH:D040181",
          "NCIT:C85865",
          "SCTID:128430005",
          "UMLS:C1138434"
        ],
        "synonyms": [
          "X-linked disease or disorder",
          "X-linked hereditary disease",
          "X-linked hereditary disorder",
          "X-linked inherited disease",
          "X-linked inherited disorder",
          "disease or disorder, X-linked",
          "disease, X-linked",
          "X linked genetic diseases",
          "X-linked genetic disease",
          "X-linked genetic diseases",
          "disease, X-linked genetic",
          "diseases, X-linked genetic",
          "genetic disease, X-linked",
          "genetic diseases, X chromosome linked",
          "genetic diseases, X linked",
          "genetic diseases, X-chromosome linked"
        ],
        "definition": "X-linked form of disease."
      },
      "child_count": 50,
      "reference_id": "MONDO:0000425"
    },
    {
      "id": 10419,
      "label": "epidermodysplasia verruciformis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6778,
        23867
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:13777",
          "GARD:0006357",
          "ICD9:078.19",
          "ICD9:757.8",
          "MEDGEN:41831",
          "MESH:D004819",
          "MedDRA:10052339",
          "NANDO:2200768",
          "NCIT:C126877",
          "Orphanet:302",
          "SCTID:19138001",
          "UMLS:C0014522",
          "icd11.foundation:1191479808"
        ],
        "synonyms": [
          "Lewandowsky-Lutz dysplasia",
          "Lewandowsky-Lutz syndrome",
          "Lutz-Lewandowsky epidermodysplasia verruciformis",
          "epidermodysplasia verruciformis",
          "EV",
          "ever"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "A rare inherited genodermatosis characterized by chronic infection with human papillomavirus (HPV) leading to polymorphous cutaneous lesions and high risk of developing non melanoma skin cancer."
      },
      "child_count": 2,
      "reference_id": "MONDO:0009176"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2902,
      "label": "X-linked disease"
    },
    {
      "id": 10419,
      "label": "epidermodysplasia verruciformis"
    }
  ]
}