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Metadata
ID	DOID:0050977
Name	spinocerebellar ataxia type 28
Definition	An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, dysarthria, hyperreflexia, ophthalmoparesis, nystagmus and ptosis, and has_material_basis_in mutation in the AFG3L2 gene. https://rarediseases.info.nih.gov/diseases/9951/spinocerebellar-ataxia-28
Xrefs	MIM:610246
Parent Relationships	is_a autosomal dominant cerebellar ataxia
Subclass Logical Relationships	has symptom some ptosis