{
  "id": 12441,
  "label": "spinocerebellar ataxia type 10",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011330",
  "properties": {
    "xrefs": [
      "DOID:0050960",
      "GARD:0010474",
      "MEDGEN:369786",
      "MESH:C566874",
      "OMIM:603516",
      "Orphanet:98761",
      "SCTID:715754007",
      "UMLS:C1963674",
      "icd11.foundation:157300879"
    ],
    "synonyms": [
      "SCA10",
      "spinocerebellar ataxia type 10",
      "spinocerebellar ataxia 10"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Spinocerebellar ataxia type 10 (SCA10) is a subtype of type I autosomal dominant cerebellar ataxia (ADCA type I). It is characterized by slowly progressive cerebellar syndrome and epilepsy, sometimes mild pyramidal signs, peripheral neuropathy and neuropsychological disturbances."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19537,
      "label": "autosomal dominant cerebellar ataxia type IV",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19840
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019254",
          "MEDGEN:1842584",
          "Orphanet:94149",
          "UMLS:C5680261"
        ],
        "synonyms": [
          "ADCA4",
          "ADCAIV",
          "autosomal dominant cerebellar ataxia type 4",
          "autosomal dominant cerebellar ataxia type IV"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0019794"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19537,
      "label": "autosomal dominant cerebellar ataxia type IV"
    }
  ]
}