{
  "id": 8458,
  "label": "NF2-related schwannomatosis",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007039",
  "properties": {
    "xrefs": [
      "DOID:0111252",
      "GARD:0007193",
      "ICD10CM:Q85.02",
      "ICD9:237.72",
      "MEDGEN:18014",
      "MedDRA:10000523",
      "MedDRA:10029271",
      "NANDO:1200227",
      "NCIT:C3274",
      "OMIM:101000",
      "Orphanet:637",
      "SCTID:92503002",
      "UMLS:C0027832",
      "icd11.foundation:14808714"
    ],
    "synonyms": [
      "acoustic neurofibromatosis",
      "NF2",
      "NF2-related schwannomatosis",
      "SWNV",
      "bilateral acoustic neurofibromatosis",
      "central neurofibromatosis",
      "full NF2",
      "full neurofibromatosis type 2",
      "neurofibromatosis 2",
      "neurofibromatosis type 2",
      "nonmosaic NF2-related schwannomatosis",
      "nonmosaic neurofibromatosis type 2",
      "acoustic Schwannomas, bilateral",
      "acoustic neurinoma bilateral",
      "acoustic neurinoma, bilateral",
      "acoustic schwannomas bilateral",
      "neurofibromatosis central type",
      "neurofibromatosis type II",
      "neurofibromatosis, central type",
      "neurofibromatosis, type 2",
      "neurofibromatosis, type II"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A tumor-prone disorder characterized by the development of multiple schwannomas and meningiomas."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 20303,
      "label": "neurofibromatosis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        16218,
        23107,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:8712",
          "EFO:0008514",
          "GARD:0010420",
          "ICD10CM:Q85.0",
          "ICD9:237.7",
          "ICD9:237.70",
          "ICDO:9540/1",
          "MEDGEN:58149",
          "MESH:D017253",
          "NANDO:1200225",
          "NANDO:1200226",
          "NANDO:1200227",
          "NANDO:2201003",
          "NCIT:C6727",
          "SCTID:19133005",
          "UMLS:C0162678"
        ],
        "synonyms": [
          "Recklinghausen's neurofibromatosis",
          "acoustic neurofibromatosis",
          "central Neurofibromatosis",
          "neurofibromatosis",
          "neurofibromatosis syndrome",
          "peripheral Neurofibromatosis",
          "type IV neurofibromatosis of riccardi",
          "von Reklinghausen disease",
          "neurofibromatosis type 2",
          "neurofibromatosis type 4",
          "neurofibromatosis type IV"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A hereditary neoplastic syndrome in which tumors grow in the nervous system. There are typically 3 main types recognized, but other forms with uncertain etiology exist."
      },
      "child_count": 20,
      "reference_id": "MONDO:0021061"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 20303,
      "label": "neurofibromatosis"
    }
  ]
}