{
  "id": 9567,
  "label": "Kindler syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008260",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 19133,
      "label": "inherited epidermolysis bullosa",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        8025,
        19129,
        23867
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018992",
          "ICD9:757.39",
          "MEDGEN:697573",
          "Orphanet:79361",
          "SCTID:402781004",
          "UMLS:C1274224"
        ],
        "synonyms": [
          "epidermolysis bullosa hereditaria",
          "hereditary epidermolysis bullosa"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Inherited epidermolysis bullosa (EB) encompasses a number of disorders characterized by recurrent blister formation as the result of structural fragility within the skin and selected other tissues."
      },
      "child_count": 12,
      "reference_id": "MONDO:0019276"
    }
  ],
  "children": [
    {
      "id": 17681,
      "label": "hereditary acrokeratotic poikiloderma, Weary type",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9567
      ],
      "type_id": 0,
      "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"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0017365"
    }
  ],
  "roots": [
    {
      "id": 19133,
      "label": "inherited epidermolysis bullosa"
    }
  ]
}