{
  "id": 13399,
  "label": "acral peeling skin syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012345",
  "properties": {
    "xrefs": [
      "DOID:0070521",
      "GARD:0012863",
      "MEDGEN:342862",
      "MESH:C536316",
      "OMIM:609796",
      "Orphanet:263534",
      "SCTID:709416009",
      "UMLS:C1853354"
    ],
    "synonyms": [
      "acral PSS",
      "acral deciduous skin",
      "acral peeling skin syndrome",
      "localised PSS",
      "localised deciduous skin",
      "localized PSS",
      "localized deciduous skin",
      "peeling skin syndrome type 2",
      "PSS2",
      "peeling skin syndrome 2",
      "peeling skin syndrome, acral type"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "Acral peeling skin syndrome (PSS) is a form of PSS characterized by superficial peeling of the skin predominantly affecting the dorsa of the hands and feet."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19185,
      "label": "peeling skin syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16624
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060283",
          "GARD:0007347",
          "ICD9:757.39",
          "MEDGEN:336530",
          "NORD:1562",
          "OMIMPS:270300",
          "Orphanet:817",
          "SCTID:239065004",
          "UMLS:C1849193",
          "icd11.foundation:523640904"
        ],
        "synonyms": [
          "PSS",
          "deciduous skin",
          "familial continuous skin peeling syndrome",
          "idiopathic deciduous skin",
          "keratosis exfoliativa congenita",
          "peeling skin disease",
          "familial continuous skin peeling",
          "skin peeling syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Peeling skin syndrome (PSS) refers to a group of rare autosomal recessive forms of ichthyosis that is characterized clinically by superficial, asymptomatic, spontaneous peeling of the skin and histologically by a shedding of the outer layers of the epidermis. PSS presents with either an acral (acral PSS) or a generalized distribution (generalized PSS type A (non inflammatory) or B (inflammatory)). Some cases remain difficult to classify, suggesting that there could be additional subtypes of PSS."
      },
      "child_count": 5,
      "reference_id": "MONDO:0019347"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19185,
      "label": "peeling skin syndrome"
    }
  ]
}