{
  "id": 8808,
  "label": "Darier disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007417",
  "properties": {
    "xrefs": [
      "DOID:2734",
      "GARD:0006243",
      "ICD9:757.39",
      "MEDGEN:5956",
      "MESH:D007644",
      "MedDRA:10023369",
      "NCIT:C84665",
      "NORD:1329",
      "OMIM:124200",
      "Orphanet:218",
      "SCTID:48611009",
      "UMLS:C0022595",
      "Wikipedia:Darier%27s_disease",
      "icd11.foundation:643994486"
    ],
    "synonyms": [
      "Darier disease",
      "Darier's disease",
      "Darier-White disease",
      "Keratosis Follicularis",
      "keratosis follicularis",
      "DAR",
      "Darier White disease",
      "Darier disease, acral hemorrhagic type",
      "Darier disease, segmental",
      "dar"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "Darier disease (DD) is a keratinization disorder characterized by the development of keratotic papules in seborrheic areas and specific nail anomalies."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19129,
      "label": "epidermal disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6820
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1842776",
          "Orphanet:79353",
          "UMLS:C5681492"
        ],
        "synonyms": [
          "epidermal disease",
          "rare epidermal disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A skin disease that involves the epidermis."
      },
      "child_count": 25,
      "reference_id": "MONDO:0019268"
    },
    {
      "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": 19129,
      "label": "epidermal disease"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder"
    }
  ]
}