{
  "id": 18054,
  "label": "erythrokeratoderma en cocardes",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0017836",
  "properties": {
    "xrefs": [
      "GARD:0001722",
      "ICD9:447.8",
      "MEDGEN:1845700",
      "Orphanet:315",
      "SCTID:239062001",
      "UMLS:C5848050"
    ],
    "synonyms": [
      "Degos genodermatosis",
      "Degos genodermatosis \"en cocardes\"",
      "Degos 'en cocarde' erythrokeratoderma",
      "Degos genodermatosis 'en cocardes'",
      "erythrokeratoderma \"en cocardes\"",
      "erythrokeratoderma ''en cocardes''",
      "erythrokeratoderma 'en cocardes'"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "Erythrokeratoderma 'en cocardes' is a rare genodermatosis characterized by circumscribed target-like (or 'en cocardes') erythematous hyperkeratotic lesions. These lesions, which remit and recur, affect the trunk and extremities and are accompanied by scaly plaques evocative of erythrokeratoderma variabilis. Onset usually occurs at birth or during early childhood. Only few cases have been described. Transmission is autosomal dominant."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19131,
      "label": "erythrokeratoderma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19129
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018986",
          "ICD9:757.39",
          "MEDGEN:609461",
          "MedDRA:10015280",
          "Orphanet:79355",
          "SCTID:254215005",
          "UMLS:C0432330"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "An umbrella term for a group of rare genetic skin disorders characterized by well-demarcated plaques of reddened, dry and thickened skin. Typically, these lesions are distributed symmetrically on the body and tend to slowly expand and progress over time."
      },
      "child_count": 6,
      "reference_id": "MONDO:0019270"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19131,
      "label": "erythrokeratoderma"
    }
  ]
}