{
  "id": 18798,
  "label": "striate palmoplantar keratoderma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018865",
  "properties": {
    "xrefs": [
      "DOID:0081105",
      "GARD:0015016",
      "MEDGEN:1631598",
      "Orphanet:50942",
      "SCTID:764958008",
      "UMLS:C4707237",
      "icd11.foundation:1171134598"
    ],
    "synonyms": [
      "keratosis palmoplantaris striata",
      "keratosis palmoplantaris striata et areata",
      "keratosis palmoplantaris varians of Wachters"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "Striate palmoplantar keratoderma is an isolated, focal, hereditary palmoplantar keratoderma characterized by linear hyperkeratosis along the flexor aspect of the fingers and on palms, as well as focal hyperkeratosis of the plantar skin. Patients present with painful thickening of the skin on palms and soles, with occasional fissuring, blistering and hyperhidrosis. Rarely, hyperkeratosis on other areas may be seen (knees, dorsal aspects of the digits). Histopatologically, widened intercellular spaces between keratinocytes are observed."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 17919,
      "label": "focal palmoplantar keratoderma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19132
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021294",
          "MEDGEN:419939",
          "Orphanet:307837",
          "UMLS:C2931923",
          "icd11.foundation:1676945961"
        ],
        "synonyms": [
          "focal PPK",
          "focal keratosis palmoplantaris",
          "focal palmoplantar hyperkeratosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ]
      },
      "child_count": 12,
      "reference_id": "MONDO:0017672"
    }
  ],
  "children": [
    {
      "id": 12958,
      "label": "keratosis palmoplantaris striata 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18798
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081110",
          "GARD:0009173",
          "MEDGEN:418996",
          "MESH:C536163",
          "OMIM:607654",
          "UMLS:C2931123"
        ],
        "synonyms": [
          "KRT1 striate palmoplantar keratoderma",
          "keratosis palmoplantaris striata type 3",
          "striate palmoplantar keratoderma caused by mutation in KRT1",
          "PPKS3",
          "keratoderma palmoplantar striate form 3",
          "keratoderma, palmoplantar, striate form 3",
          "keratosis palmoplantaris striata III",
          "striate palmoplantar keratoderma 3"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Any striate palmoplantar keratoderma in which the cause of the disease is a mutation in the KRT1 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011881"
    },
    {
      "id": 14072,
      "label": "keratosis palmoplantaris striata 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18798
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0081109",
          "GARD:0015590",
          "MEDGEN:343725",
          "MESH:C565102",
          "OMIM:612908",
          "UMLS:C1852127"
        ],
        "synonyms": [
          "DSP striate palmoplantar keratoderma",
          "keratosis palmoplantaris striata type 2",
          "striate palmoplantar keratoderma caused by mutation in DSP",
          "PPKS2",
          "keratoderma, palmoplantar, striate form 2",
          "keratosis palmoplantaris striata II",
          "striate palmoplantar keratoderma 2"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Any striate palmoplantar keratoderma in which the cause of the disease is a mutation in the DSP gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0013034"
    }
  ],
  "roots": [
    {
      "id": 17919,
      "label": "focal palmoplantar keratoderma"
    }
  ]
}