{
  "id": 21493,
  "label": "peeling skin syndrome 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0024548",
  "properties": {
    "xrefs": [
      "DOID:0070520",
      "GARD:0017259",
      "MEDGEN:1885521",
      "OMIM:270300",
      "Orphanet:263553",
      "UMLS:C5679693"
    ],
    "synonyms": [
      "CDSN peeling skin syndrome",
      "PSS type B",
      "generalised deciduous skin type B",
      "generalised peeling skin syndrome type B",
      "generalized deciduous skin type B",
      "generalized peeling skin syndrome type B",
      "inflammatory peeling skin syndrome",
      "peeling skin syndrome 1",
      "peeling skin syndrome caused by mutation in CDSN",
      "peeling skin syndrome type B",
      "PSS",
      "PSS1",
      "deciduous skin",
      "keratolysis exfoliativa congenita",
      "skin peeling, familial continuous generalised",
      "skin peeling, familial continuous generalized"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "Any peeling skin syndrome in which the cause of the disease is a mutation in the CDSN gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 11227,
      "label": "generalized peeling skin syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19185
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0012862",
          "MEDGEN:930825",
          "Orphanet:263543",
          "SCTID:718749004",
          "UMLS:C4305156"
        ],
        "synonyms": [
          "generalised PSS",
          "generalised deciduous skin",
          "generalized PSS",
          "generalized deciduous skin",
          "peeling skin syndrome type 1",
          "PSS1",
          "peeling skin syndrome 1"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Generalized peeling skin syndrome (PSS) is a form of PSS presenting with a generalized distribution. It comprises two sub-types: the non-inflammatory (PSS type A) and the inflammatory (PSS type B) form. PSS type A is characterized by generalized white scaling with superficial peeling of the skin, while PSS type B is characterized by superficial patchy peeling of the entire skin with underlying erythroderma, associated with pruritus, and atopy."
      },
      "child_count": 3,
      "reference_id": "MONDO:0010033"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 11227,
      "label": "generalized peeling skin syndrome"
    }
  ]
}