{
  "id": 17681,
  "label": "hereditary acrokeratotic poikiloderma, Weary type",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0017365",
  "properties": {
    "xrefs": [
      "GARD:0018781",
      "MEDGEN:96059",
      "Orphanet:2907",
      "UMLS:C0406556",
      "icd11.foundation:837824031"
    ],
    "synonyms": [
      "congenital poikiloderma with bullae, Weary type"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 9567,
      "label": "Kindler syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19133
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060472",
          "GARD:0004391",
          "MEDGEN:96060",
          "MESH:C536321",
          "NANDO:1200239",
          "OMIM:173650",
          "Orphanet:2908",
          "SCTID:238836000",
          "UMLS:C0406557",
          "icd11.foundation:726317303"
        ],
        "synonyms": [
          "KS",
          "Kindler syndrome",
          "poikiloderma of Kindler",
          "KINDLER syndrome",
          "KNDLRS",
          "bullous acrokeratotic poikiloderma of Kindler and Weary",
          "congenital bullous poikiloderma",
          "poikiloderma, congenital, with bullae, Weary type",
          "poikiloderma, hereditary acrokeratotic"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Kindler syndrome (KS) is the fourth major type of epidermolysis bullosa (EB), besides simplex, junctional and dystrophic forms, and is characterized by skin fragility and blistering at birth followed by development of photosensitivity and progressive poikilodermatous skin changes."
      },
      "child_count": 1,
      "reference_id": "MONDO:0008260"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 9567,
      "label": "Kindler syndrome"
    }
  ]
}