{
  "id": 9596,
  "label": "porokeratosis 1, Mibelli type",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008290",
  "properties": {
    "xrefs": [
      "GARD:0015108",
      "OMIM:175800"
    ],
    "synonyms": [
      "POROK1",
      "porokeratosis 1, MIBELLI type",
      "porokeratosis 1, multiple types",
      "porokeratosis of Mibelli"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19019,
      "label": "porokeratosis of Mibelli",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        8077
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0004438",
          "ICD9:757.39",
          "MEDGEN:181842",
          "Orphanet:735",
          "SCTID:80432009",
          "UMLS:C0949506"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "Porokeratosis of Mibelli (PM) is a form of porokeratosis that is characterized by the presence of brown single or multiple annular plaques of varying size, that are sometimes confluent, with a distinctive sharply-defined keratotic border."
      },
      "child_count": 2,
      "reference_id": "MONDO:0019141"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19019,
      "label": "porokeratosis of Mibelli"
    }
  ]
}