{
  "id": 2908,
  "label": "cerebellar ataxia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0000437",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 7073,
      "label": "movement disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:480",
          "EFO:0004280",
          "ICD9:333.90",
          "ICD9:333.99",
          "MEDGEN:10113",
          "MESH:D009069",
          "NCIT:C116757",
          "SCTID:60342002",
          "UMLS:C0026650"
        ],
        "synonyms": [
          "movement disease",
          "movement disorder",
          "movement disorders"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Neurological conditions resulting in abnormal voluntary or involuntary movement, which may impact the speed, fluency, quality and ease of movement."
      },
      "child_count": 54,
      "reference_id": "MONDO:0005395"
    },
    {
      "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"
    },
    {
      "id": 24044,
      "label": "atactic disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "ataxic disorder",
          "ataxia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A central nervous system disease that consists of gait impairment, unclear (“scanning”) speech, visual blurring due to nystagmus, hand incoordination, and tremor with movement."
      },
      "child_count": 4,
      "reference_id": "MONDO:0100308"
    }
  ],
  "children": [
    {
      "id": 24046,
      "label": "hereditary cerebellar ataxia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2908,
        21292,
        24045
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026137",
          "MEDGEN:78726",
          "NCIT:C140268",
          "UMLS:C0270749"
        ],
        "synonyms": [
          "cerebellar hereditary ataxia",
          "hereditary cerebellar ataxia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Cerebellar ataxia that is transmitted from parent to child."
      },
      "child_count": 15,
      "reference_id": "MONDO:0100310"
    }
  ],
  "roots": [
    {
      "id": 7073,
      "label": "movement disorder"
    },
    {
      "id": 20940,
      "label": "cerebellar degeneration"
    },
    {
      "id": 24044,
      "label": "atactic disorder"
    }
  ]
}