{
  "id": 25848,
  "label": "basal cell nevus syndrome 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0958174",
  "properties": {
    "xrefs": [
      "GARD:0026952",
      "OMIM:109400"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 8594,
      "label": "nevoid basal cell carcinoma syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        16218,
        19507,
        23107,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070365",
          "DOID:2512",
          "GARD:0007166",
          "MEDGEN:2554",
          "MESH:D001478",
          "MedDRA:10062804",
          "NANDO:2200828",
          "NCIT:C2892",
          "NORD:1507",
          "OMIMPS:109400",
          "Orphanet:377",
          "SCTID:69408002",
          "UMLS:C0004779",
          "icd11.foundation:1012745138"
        ],
        "synonyms": [
          "Gorlin syndrome",
          "Gorlin-Goltz syndrome",
          "NBCCS",
          "basal cell nevus syndrome",
          "multiple basal cell carcinomas",
          "nevoid basal cell cancer syndrome",
          "nevoid basal cell carcinoma syndrome",
          "BCNS",
          "multiple basal cell nevi, odontogenic keratocysts, and skeletal anomalies"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare hereditary disorder due to autosomal dominant transmission with hamartosis characterized by multiple early-onset basal cell carcinoma (BCC), multiple jaw keratocysts and skeletal abnormalities."
      },
      "child_count": 10,
      "reference_id": "MONDO:0007187"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 8594,
      "label": "nevoid basal cell carcinoma syndrome"
    }
  ]
}