{
  "id": 20940,
  "label": "cerebellar degeneration",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0022687",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 4515,
      "label": "cerebellar disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7209
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 5,
      "reference_id": "MONDO:0002427"
    },
    {
      "id": 7208,
      "label": "neurodegenerative disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4657
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1289",
          "EFO:0005772",
          "ICD9:349.89",
          "MEDGEN:17999",
          "MESH:D019636",
          "NCIT:C4802",
          "SCTID:80690008",
          "UMLS:C0027746"
        ],
        "synonyms": [
          "degenerative disease",
          "brain degeneration",
          "central nervous system degenerative disorder",
          "central nervous system neurodegenerative disorder",
          "degenerative disorder of central nervous system",
          "cerebral degeneration disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A disorder of the central nervous system characterized by gradual and progressive loss of neural tissue and neurologic function."
      },
      "child_count": 22,
      "reference_id": "MONDO:0005559"
    }
  ],
  "children": [
    {
      "id": 2908,
      "label": "cerebellar ataxia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7073,
        20940,
        24044
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050753",
          "GARD:0019816",
          "ICD9:334.3",
          "MEDGEN:849",
          "MESH:D002524",
          "NANDO:1200037",
          "NANDO:2100238",
          "NANDO:2200882",
          "NCIT:C82341",
          "Orphanet:102002",
          "SCTID:85102008",
          "UMLS:C0007758"
        ],
        "synonyms": [
          "ataxia syndrome",
          "cerebellar ataxias",
          "spinocerebellar ataxia",
          "spinocerebellar degeneration",
          "ataxia",
          "ataxia, cerebellar",
          "ataxias, cerebellar",
          "cerebellar dysmetria",
          "cerebellar dysmetrias",
          "rare ataxia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A neurological syndrome characterized by clumsy and uncoordinated movement of the limbs, trunk, and cranial muscles. It results from pathology in the cerebellum and its connections, or in the proprioceptive sensory pathways."
      },
      "child_count": 3,
      "reference_id": "MONDO:0000437"
    },
    {
      "id": 23463,
      "label": "paraneoplastic cerebellar degeneration",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18348,
        20940
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022493",
          "MEDGEN:98273",
          "MESH:D020362",
          "NCIT:C4685",
          "Orphanet:623626",
          "UMLS:C0393534",
          "icd11.foundation:1087616692"
        ],
        "synonyms": [
          "paraneoplastic cerebellar degeneration"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare, immune-mediated disorder characterized by cerebellar degeneration due to the presence of an often undetected malignancy (usually carcinoma or lymphoma) in an anatomic site other than the cerebellum. Signs and symptoms include progressive ataxia, dysarthria, and nystagmus."
      },
      "child_count": 0,
      "reference_id": "MONDO:0044877"
    }
  ],
  "roots": [
    {
      "id": 4515,
      "label": "cerebellar disorder"
    },
    {
      "id": 7208,
      "label": "neurodegenerative disease"
    }
  ]
}