{
  "id": 12151,
  "label": "Cayman type cerebellar ataxia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011025",
  "properties": {
    "xrefs": [
      "DOID:0060694",
      "GARD:0016836",
      "MEDGEN:331319",
      "MESH:C563363",
      "OMIM:601238",
      "Orphanet:94122",
      "SCTID:717332007",
      "UMLS:C1832585"
    ],
    "synonyms": [
      "Cayman ataxia",
      "Cayman type cerebellar ataxia",
      "ataxia, cerebellar, Cayman type",
      "ATCAY",
      "cerebellar ataxia, CAYMAN type",
      "cerebellar ataxia, Cayman type"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Cerebellar ataxia, Cayman type is characterized by psychomotor retardation, hypotonia and cerebellar dysfunction (nystagmus, ataxic gait, truncal ataxia, dysarthric speech and intention tremor), associated with cerebellar hypoplasia."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19711,
      "label": "autosomal recessive congenital cerebellar ataxia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16133
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019412",
          "MEDGEN:1843070",
          "Orphanet:98095",
          "UMLS:C5681519"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 7,
      "reference_id": "MONDO:0020043"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19711,
      "label": "autosomal recessive congenital cerebellar ataxia"
    }
  ]
}