{
  "id": 15330,
  "label": "palmoplantar keratoderma, nonepidermolytic, focal or diffuse",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014327",
  "properties": {
    "xrefs": [
      "DOID:0111710",
      "GARD:0017669",
      "MEDGEN:816724",
      "OMIM:615735",
      "Orphanet:402003",
      "UMLS:C3810394"
    ],
    "synonyms": [
      "autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering",
      "palmoplantar keratoderma, nonepidermolytic, focal or diffuse",
      "PPKNEFD"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19132,
      "label": "hereditary palmoplantar keratoderma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        8066,
        19129,
        23867
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018988",
          "ICD9:757.39",
          "MEDGEN:590657",
          "Orphanet:79357",
          "SCTID:239066003",
          "UMLS:C0406757",
          "icd11.foundation:1941547119"
        ],
        "synonyms": [
          "hereditary PPK",
          "hereditary keratosis palmoplantaris",
          "hereditary palmoplantar hyperkeratosis",
          "hereditary palmoplantar keratosis"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "An instance of palmoplantar keratosis that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 24,
      "reference_id": "MONDO:0019272"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19132,
      "label": "hereditary palmoplantar keratoderma"
    }
  ]
}