{
  "id": 14425,
  "label": "autosomal recessive spinocerebellar ataxia 10",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013392",
  "properties": {
    "xrefs": [
      "DOID:0050999",
      "GARD:0017314",
      "MEDGEN:462348",
      "OMIM:613728",
      "Orphanet:284289",
      "UMLS:C3150998"
    ],
    "synonyms": [
      "ANO10 autosomal recessive cerebellar ataxia",
      "SCAR10",
      "autosomal recessive cerebellar ataxia caused by mutation in ANO10",
      "autosomal recessive spinocerebellar ataxia type 10",
      "spinocerebellar ataxia, autosomal recessive type 10",
      "adult-onset autosomal recessive cerebellar ataxia",
      "spinocerebellar ataxia, autosomal recessive 10"
    ],
    "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 ANO10 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"
    }
  ]
}