{
  "id": 11254,
  "label": "spinocerebellar degeneration with slow eye movements",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010065",
  "properties": {
    "xrefs": [
      "GARD:0024704",
      "OMIM:271322"
    ],
    "synonyms": [
      "spinocerebellar degeneration with slow eye movements",
      "SDSEM"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 9750,
      "label": "spinocerebellar ataxia type 2",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6868,
        16361,
        19535
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050955",
          "DOID:0060204",
          "GARD:0004072",
          "MEDGEN:155704",
          "NANDO:1200046",
          "NCIT:C148315",
          "OMIM:183090",
          "Orphanet:98756",
          "SCTID:715751004",
          "UMLS:C0752121",
          "icd11.foundation:1232187870"
        ],
        "synonyms": [
          "ATXN2 autosomal dominant cerebellar ataxia type I",
          "OPCA2",
          "SCA2",
          "autosomal dominant cerebellar ataxia type I caused by mutation in ATXN2",
          "spinocerebellar ataxia type 2",
          "ALS13",
          "SCA 2",
          "Wadia swami syndrome",
          "Wadia-swami syndrome",
          "amyotrophic lateral sclerosis 13",
          "amyotrophic lateral sclerosis type 13",
          "amyotrophic lateral sclerosis, susceptibility to, 13",
          "cerebellar Degeneration with slow eye movements",
          "olivopontocerebellar atrophy 2",
          "olivopontocerebellar atrophy Holguin type",
          "olivopontocerebellar atrophy, Holguin type",
          "spinocerebellar Degeneration with slow eye movements",
          "spinocerebellar ataxia 2",
          "spinocerebellar ataxia Cuban type",
          "spinocerebellar ataxia with slow eye movements",
          "spinocerebellar ataxia, Cuban type",
          "spinocerebellar atrophy 2"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A subtype of type I autosomal dominant cerebellar ataxia (ADCA type I) characterized by truncal ataxia, dysarthria, slowed saccades and less commonly ophthalmoparesis and chorea."
      },
      "child_count": 3,
      "reference_id": "MONDO:0008458"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 9750,
      "label": "spinocerebellar ataxia type 2"
    }
  ]
}