{
  "id": 17080,
  "label": "acquired ataxia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016593",
  "properties": {
    "xrefs": [
      "GARD:0020656",
      "MEDGEN:927781",
      "Orphanet:247242",
      "SCTID:722968003",
      "UMLS:C4302112",
      "icd11.foundation:71197968"
    ],
    "synonyms": [
      "acquired ataxia"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A type of ataxia that is acquired during the lifetime of the individual."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "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": 17079,
      "label": "sporadic adult-onset ataxia of unknown etiology",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17080
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020654",
          "MEDGEN:1383968",
          "Orphanet:247234",
          "SCTID:734023003",
          "UMLS:C4518339"
        ],
        "synonyms": [
          "SAOA",
          "idiopathic late-onset cerebellar ataxia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Sporadic adult-onset ataxia of unknown etiology describes a group of non-hereditary degenerative ataxias characterized by a slowly progressive cerebellar syndrome (with ataxia of stance and gait, upper limb dysmetria and intention tremor, ataxic speech, and oculomotor abnormalities), presenting in adulthood (at around 50 years of age), that is not due to a known cause. Extracerebellar symptoms (e.g., decreased vibration sense and absent or decreased ankle reflexes), polyneuropathy and mild autonomic dysfunction may also be present. Mild cognitive impairment has also rarely been reported."
      },
      "child_count": 0,
      "reference_id": "MONDO:0016591"
    },
    {
      "id": 25556,
      "label": "immune-mediated cerebellar ataxia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        17080
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022494",
          "MEDGEN:1814462",
          "Orphanet:623638",
          "UMLS:C5680410"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0859692"
    }
  ],
  "roots": [
    {
      "id": 24044,
      "label": "atactic disorder"
    }
  ]
}