{
  "id": 16762,
  "label": "spinocerebellar ataxia 7",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016163",
  "properties": {
    "xrefs": [
      "DOID:0050958",
      "GARD:0020405",
      "MEDGEN:156006",
      "NCIT:C126562",
      "OMIM:164500",
      "Orphanet:208508",
      "Orphanet:94147",
      "SCTID:715726000",
      "UMLS:C0752125"
    ],
    "synonyms": [
      "ADCA2",
      "ADCAII",
      "ATXN7 autosomal dominant cerebellar ataxia type II",
      "SCA7",
      "ataxia with pigmentary retinopathy",
      "autosomal dominant cerebellar ataxia type 2",
      "autosomal dominant cerebellar ataxia type II",
      "autosomal dominant cerebellar ataxia type II caused by mutation in ATXN7",
      "cerebellar syndrome-pigmentary maculopathy syndrome",
      "spinocerebellar ataxia 7",
      "spinocerebellar ataxia type 7",
      "ADCA, type II",
      "Adca, type 2",
      "OPCA 3",
      "OPCA III",
      "OPCA with macular Degeneration and external ophthalmoplegia",
      "OPCA with retinal Degeneration",
      "OPCA3",
      "autosomal dominant cerebellar ataxia, type 2",
      "olivopontocerebellar atrophy 3"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19840,
      "label": "autosomal dominant cerebellar ataxia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        16360,
        24046
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:1441",
          "GARD:0004346",
          "ICD9:334.3",
          "MEDGEN:1684639",
          "NORD:825",
          "OMIMPS:164400",
          "Orphanet:99",
          "SCTID:129609000",
          "UMLS:C4087347"
        ],
        "synonyms": [
          "SCA",
          "spinocerebellar ataxia",
          "ADCA",
          "Autosomal Dominant Hereditary Ataxia",
          "autosomal dominant spinocerebellar ataxia",
          "cerebellar ataxia, autosomal dominant",
          "Pierre Marie cerebellar ataxia (formerly)"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A clinically and genetically heterogeneous group of neurodegenerative diseases characterized by a slowly progressive ataxia of gait, stance and limbs, dysarthria and/or oculomotor disorder, due to cerebellar degeneration in the absence of coexisting diseases. The degenerative process can be limited to the cerebellum (ADCA type 3) or may additionally involve the retina (ADCA type 2), optic nerve, ponto-medullary systems, basal ganglia, cerebral cortex, spinal tracts or peripheral nerves (ADCA type 1). In ACDA type 4, a cerebellar syndrome is associated with epilepsy."
      },
      "child_count": 45,
      "reference_id": "MONDO:0020380"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19840,
      "label": "autosomal dominant cerebellar ataxia"
    }
  ]
}