{
  "id": 9236,
  "label": "lichen planus, familial",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007902",
  "properties": {
    "xrefs": [
      "MEDGEN:372036",
      "MESH:C563624",
      "OMIM:151620",
      "UMLS:C1835402"
    ],
    "synonyms": [
      "hereditary lichen planus",
      "lichen planus, familial"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "An instance of lichen planus that is caused by an inherited modification of the individual's genome."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 8052,
      "label": "lichen planus",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4496,
        8050
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:9201",
          "EFO:1000726",
          "ICD10CM:L43",
          "ICD10WHO:L43",
          "ICD9:697.0",
          "MEDGEN:9753",
          "MESH:D008010",
          "NCIT:C3189",
          "SCTID:4776004",
          "UMLS:C0023646",
          "icd11.foundation:1402978031"
        ],
        "synonyms": [
          "lichen ruber planus",
          "ruber planus"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A chronic, recurrent, pruritic inflammatory disorder of unknown etiology that affects the skin and mucus membranes. It presents with rashes and papules that tend to resolve spontaneously. It may be associated with hepatitis C. Certain drugs that contain arsenic or bismuth are associated with reactions mimicking lichen planus."
      },
      "child_count": 22,
      "reference_id": "MONDO:0006572"
    },
    {
      "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": [],
  "roots": [
    {
      "id": 8052,
      "label": "lichen planus"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder"
    }
  ]
}