{
  "id": 23088,
  "label": "sacral hemangiomas multiple congenital abnormalities",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0042961",
  "properties": {
    "xrefs": [
      "GARD:0000317",
      "MEDGEN:419414",
      "MESH:C537222",
      "UMLS:C2931443"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16696,
      "label": "Cowden disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        23867
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:6457",
          "GARD:0006202",
          "MEDGEN:5420",
          "MESH:D006223",
          "MedDRA:10051906",
          "NANDO:2200918",
          "NCIT:C3076",
          "OMIMPS:158350",
          "Orphanet:201",
          "SCTID:58037000",
          "UMLS:C0018553"
        ],
        "synonyms": [
          "Cowden disease",
          "Cowden syndrome",
          "Cowden's disease",
          "multiple hamartoma syndrome",
          "CD",
          "MHAM",
          "dysplastic gangliocytoma of cerebellum"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A genodermatosis characterized by the presence of multiple hamartomas in various tissues and an increased risk for malignancies of the breast, thyroid, endometrium, kidney and colorectum. When CS is accompanied by germline PTEN mutations, it belongs to the PTEN hamartoma tumor syndrome (PHTS) group."
      },
      "child_count": 16,
      "reference_id": "MONDO:0016063"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16696,
      "label": "Cowden disease"
    }
  ]
}