{
  "id": 15830,
  "label": "spinocerebellar ataxia, autosomal recessive 23",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014846",
  "properties": {
    "xrefs": [
      "DOID:0111613",
      "GARD:0017677",
      "MEDGEN:1667331",
      "OMIM:616949",
      "Orphanet:404493",
      "UMLS:C4750914"
    ],
    "synonyms": [
      "SCAR23",
      "autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome due to TUD deficiency",
      "spinocerebellar ataxia autosomal recessive type 23",
      "spinocerebellar ataxia, autosomal recessive 23",
      "spinocerebellar ataxia, autosomal recessive type 23"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18492,
      "label": "autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16133,
        16437
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021719",
          "MEDGEN:1843349",
          "Orphanet:404481",
          "UMLS:C5681145"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 6,
      "reference_id": "MONDO:0018446"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18492,
      "label": "autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome"
    }
  ]
}