{
  "id": 24044,
  "label": "atactic disorder",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0100308",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 4,
  "parents": [
    {
      "id": 6799,
      "label": "nervous system disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:863",
          "EFO:0000618",
          "ICD10CM:G00-G99",
          "ICD9:349.89",
          "ICD9:349.9",
          "MEDGEN:14336",
          "MESH:D009422",
          "NCIT:C26835",
          "SCTID:118940003",
          "UMLS:C0027765",
          "Wikipedia:Nervous_system_disease"
        ],
        "synonyms": [
          "disease of nervous system",
          "disease or disorder of nervous system",
          "disorder of nervous system",
          "nervous system disease",
          "nervous system disease or disorder",
          "nervous system disorder",
          "neurologic disease",
          "neurologic disorder",
          "neurological disease",
          "neurological disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A non-neoplastic or neoplastic disorder that affects the brain, spinal cord, or peripheral nerves."
      },
      "child_count": 72,
      "reference_id": "MONDO:0005071"
    }
  ],
  "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": 17080,
      "label": "acquired ataxia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24044
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 2,
      "reference_id": "MONDO:0016593"
    },
    {
      "id": 24045,
      "label": "hereditary ataxia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24044,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050951",
          "EFO:0009671",
          "GARD:0020286",
          "ICD10CM:G11",
          "ICD10WHO:G11",
          "MEDGEN:2478",
          "MESH:C531684",
          "Orphanet:183518",
          "SCTID:763597000",
          "UMLS:C0004138",
          "icd11.foundation:442347652"
        ],
        "synonyms": [
          "rare hereditary ataxia",
          "SCA"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An instance of an atactic disorder that is caused by an inherited genomic modification in an individual."
      },
      "child_count": 40,
      "reference_id": "MONDO:0100309"
    },
    {
      "id": 24047,
      "label": "sensory ataxia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24044
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:66020",
          "UMLS:C0240991"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any ataxia in which the causes of the disease is a perturbation of the sensory system, leading to its dysfunction."
      },
      "child_count": 2,
      "reference_id": "MONDO:0100311"
    }
  ],
  "roots": [
    {
      "id": 6799,
      "label": "nervous system disorder"
    }
  ]
}