{
  "id": 14670,
  "label": "autosomal recessive spinocerebellar ataxia 11",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013645",
  "properties": {
    "xrefs": [
      "DOID:0080063",
      "GARD:0017312",
      "MEDGEN:1681191",
      "OMIM:614229",
      "Orphanet:284271",
      "UMLS:C5190803"
    ],
    "synonyms": [
      "SCAR11",
      "SYT14 autosomal recessive syndromic cerebellar ataxia",
      "autosomal recessive spinocerebellar ataxia 11",
      "autosomal recessive spinocerebellar ataxia type 11",
      "autosomal recessive syndromic cerebellar ataxia caused by mutation in SYT14",
      "spinocerebellar ataxia, autosomal recessive type 11",
      "autosomal recessive cerebellar ataxia-psychomotor retardation syndrome",
      "spinocerebellar ataxia, autosomal recessive 11"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Any autosomal recessive syndromic cerebellar ataxia in which the cause of the disease is a mutation in the SYT14 gene."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19714,
      "label": "autosomal recessive syndromic cerebellar ataxia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16133
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019416",
          "MEDGEN:1843251",
          "Orphanet:98099",
          "UMLS:C5681516"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 7,
      "reference_id": "MONDO:0020047"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19714,
      "label": "autosomal recessive syndromic cerebellar ataxia"
    }
  ]
}