{
  "id": 15913,
  "label": "spinocerebellar ataxia, autosomal recessive 24",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014934",
  "properties": {
    "xrefs": [
      "DOID:0111615",
      "GARD:0025035",
      "MEDGEN:934666",
      "OMIM:617133",
      "UMLS:C4310699"
    ],
    "synonyms": [
      "SCAR24",
      "UBA5 autosomal recessive cerebellar ataxia",
      "autosomal recessive cerebellar ataxia caused by mutation in UBA5",
      "spinocerebellar ataxia, autosomal recessive 24",
      "spinocerebellar ataxia, autosomal recessive 24; SCAR24",
      "spinocerebellar ataxia, autosomal recessive type 24"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any autosomal recessive cerebellar ataxia in which the cause of the disease is a mutation in the UBA5 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16133,
      "label": "autosomal recessive cerebellar ataxia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7611,
        24046
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050950",
          "GARD:0018718",
          "MEDGEN:1843058",
          "OMIMPS:213200",
          "Orphanet:1172",
          "UMLS:C5575375"
        ],
        "synonyms": [
          "ARCA",
          "arca",
          "cerebellar ataxia, autosomal recessive"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Autosomal recessive cerebellar ataxias (ARCA) are a heterogeneous group of rare neurological disorders involving both the central and peripheral nervous system (and in some cases other systems and organs), and characterized by degeneration or abnormal development of the cerebellum and spinal cord and, in most cases, early onset occurring before the age of 20 years."
      },
      "child_count": 58,
      "reference_id": "MONDO:0015244"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16133,
      "label": "autosomal recessive cerebellar ataxia"
    }
  ]
}