{
  "id": 4515,
  "label": "cerebellar disorder",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0002427",
  "properties": {
    "xrefs": [
      "DOID:2786",
      "MEDGEN:40186",
      "MESH:D002526",
      "SCTID:223176004",
      "UMLS:C0007760"
    ],
    "synonyms": [
      "cerebellum disease",
      "cerebellum disease or disorder",
      "disease of cerebellum",
      "disease or disorder of cerebellum",
      "disorder of cerebellum"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Diseases that affect the structure or function of the cerebellum. Cardinal manifestations of cerebellar dysfunction include dysmetria, gait ataxia, and muscle hypotonia."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 5,
  "parents": [
    {
      "id": 7209,
      "label": "brain disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4657
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:936",
          "EFO:0005774",
          "ICD9:348.3",
          "ICD9:348.30",
          "ICD9:348.8",
          "ICD9:348.9",
          "MEDGEN:14214",
          "MESH:D001927",
          "NCIT:C96413",
          "SCTID:81308009",
          "UMLS:C0006111"
        ],
        "synonyms": [
          "brain disease",
          "brain disease or disorder",
          "disease of brain",
          "disease or disorder of brain",
          "disorder of brain",
          "encephalopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A disease affecting the brain or part of the brain."
      },
      "child_count": 71,
      "reference_id": "MONDO:0005560"
    }
  ],
  "children": [
    {
      "id": 4920,
      "label": "cerebellar neoplasm",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4515,
        20429
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:4205",
          "MEDGEN:40187",
          "MESH:D002528",
          "NCIT:C2935",
          "SCTID:126960003",
          "UMLS:C0007762"
        ],
        "synonyms": [
          "cerebellar neoplasm",
          "cerebellar tumor",
          "cerebellar tumour",
          "cerebellum neoplasm",
          "cerebellum neoplasm (disease)",
          "cerebellum tumor",
          "cerebellum tumour",
          "neoplasm of cerebellum",
          "neoplasm of the cerebellum",
          "tumor of cerebellum",
          "tumor of the cerebellum",
          "tumour of cerebellum",
          "tumour of the cerebellum",
          "malignant tumor of cerebellum",
          "malignant tumour of cerebellum",
          "cerebellum cancer"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A benign or malignant (primary or metastatic) tumor involving the cerebellum. -- 2003"
      },
      "child_count": 16,
      "reference_id": "MONDO:0002913"
    },
    {
      "id": 7462,
      "label": "Miller Fisher syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2996,
        4370,
        4515
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:12889",
          "EFO:0007371",
          "GARD:0003668",
          "MEDGEN:95994",
          "MESH:D019846",
          "MedDRA:10049567",
          "NCIT:C116958",
          "Orphanet:98919",
          "SCTID:1767005",
          "UMLS:C0393799",
          "icd11.foundation:134795253"
        ],
        "synonyms": [
          "Fisher syndrome",
          "Guillain Barre syndrome, Miller Fisher variant",
          "Guillain-Barre syndrome, Miller Fisher variant",
          "Miller Fisher variant of Guillain Barre syndrome",
          "Miller-Fisher syndrome",
          "cranial variant of GBS",
          "cranial variant of Guillain-Barre syndrome",
          "cranial variant of Guillain-Barré syndrome",
          "ophthalmoplegia, ataxia and areflexia syndrome",
          "syndrome, Fisher",
          "syndrome, Miller Fisher",
          "syndrome, Miller-Fisher"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An autoimmune process characterized by the clinical triad of ophthalmoplegia, ataxia, and areflexia."
      },
      "child_count": 0,
      "reference_id": "MONDO:0005851"
    },
    {
      "id": 10321,
      "label": "Dandy-Walker syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4515,
        19751
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2785",
          "EFO:1000890",
          "GARD:0006242",
          "MEDGEN:4150",
          "MESH:D003616",
          "MedDRA:10048411",
          "NANDO:2200821",
          "NCIT:C75012",
          "NORD:1032",
          "OMIM:220200",
          "Orphanet:217",
          "SCTID:14447001",
          "UMLS:C0010964",
          "icd11.foundation:993088960"
        ],
        "synonyms": [
          "Dandy Walker Malformation",
          "Dandy-Walker syndrome",
          "Dandy-Walker syndrome, Isolated cases",
          "DW complex",
          "DWS",
          "Dandy-Walker complex",
          "Dandy-Walker malformation",
          "Dandy-Walker syndrome or malformation (type of DW complex)",
          "Dandy-Walker variant (type of DW complex)",
          "isolated Dandy-Walker malformation",
          "mega cisterna magna (type of DW complex)"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Dandy-Walker malformation (DWM) is the association of three signs: hydrocephalus, partial or complete absence of the cerebellar vermis, and posterior fossa cyst contiguous with the fourth ventricle, presenting early in life with hydrocephalus, bulging occiput and posterior fossa signs such as cranial nerve palsies, nystagmus and ataxia."
      },
      "child_count": 6,
      "reference_id": "MONDO:0009072"
    },
    {
      "id": 20888,
      "label": "Behrens Baumann dust syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4515,
        16704,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0004021",
          "MEDGEN:444092",
          "MESH:C537670",
          "UMLS:C2931582"
        ],
        "synonyms": [
          "Behrens-Baumann-Vogel syndrome",
          "oculo-cerebral dysplasia",
          "microphthalmia-optic nerve dysplasia",
          "unilateral aplasia of the optic nerve with cryptophthalmus and contralateral microphthalmus"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0022557"
    },
    {
      "id": 20940,
      "label": "cerebellar degeneration",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4515,
        7208
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1443",
          "MEDGEN:75496",
          "NCIT:C84624",
          "SCTID:95646004",
          "UMLS:C0262404"
        ],
        "synonyms": [
          "cerebellar Degeneration",
          "cerebellar degeneration",
          "cerebellum neurodegenerative disease",
          "neurodegenerative disease of cerebellum",
          "cerebral degeneration"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Degeneration of the cerebellum. It may be an inherited condition, a paraneoplastic syndrome, or secondary to autoimmune disorders."
      },
      "child_count": 4,
      "reference_id": "MONDO:0022687"
    }
  ],
  "roots": [
    {
      "id": 7209,
      "label": "brain disorder"
    }
  ]
}