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DO Term : spinocerebellar ataxia type 15 [DOID:0050965] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, nystagmus, dysarthria and dysphagia, has_material_basis_in mutation in the ITPR1 gene.
  • synonyms:
  • OMIM:606658,
  • 606658,
  • DOID:0050966,
  • spinocerebellar ataxia type 16
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