{
  "id": 10419,
  "label": "epidermodysplasia verruciformis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009176",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 6778,
      "label": "immune system disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2914",
          "EFO:0000540",
          "ICD9:279",
          "ICD9:279.1",
          "ICD9:279.10",
          "ICD9:279.19",
          "ICD9:279.4",
          "ICD9:279.49",
          "ICD9:279.8",
          "ICD9:279.9",
          "MEDGEN:5759",
          "MESH:D007154",
          "NANDO:1100004",
          "NANDO:2100202",
          "NCIT:C3507",
          "SCTID:414029004",
          "UMLS:C0021053"
        ],
        "synonyms": [
          "disease of immune system",
          "disease or disorder of immune system",
          "disorder of immune system",
          "immune disease",
          "immune disorder",
          "immune dysfunction",
          "immune system disease or disorder",
          "immune system disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "A disorder resulting from an abnormality in the immune system."
      },
      "child_count": 47,
      "reference_id": "MONDO:0005046"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6820
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MESH:D012873",
          "SCTID:239001006"
        ],
        "synonyms": [
          "disease, genetic skin",
          "diseases, genetic skin",
          "genetic skin disease",
          "genetic skin diseases",
          "genodermatosis",
          "skin disease, genetic"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "An instance of skin disease that is caused by a modification of the individual's genome."
      },
      "child_count": 228,
      "reference_id": "MONDO:0100118"
    }
  ],
  "children": [
    {
      "id": 11740,
      "label": "epidermodysplasia verruciformis, X-linked",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2902,
        10419
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010587"
    }
  ],
  "roots": [
    {
      "id": 6778,
      "label": "immune system disorder"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder"
    }
  ]
}