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Metadata
ID	DOID:0050999
Name	autosomal recessive spinocerebellar ataxia 10
Definition	An autosomal recessive cerebellar ataxia that is characterized by ataxia, dysarthria, nystagmus and marked cerebellar atrophy, has_material_basis_in mutation in the ANO10 gene. https://www.omim.org/entry/613728
Xrefs	OMIM:613728
Synonyms	SCAR10 [EXACT]
Parent Relationships	is_a autosomal recessive cerebellar ataxia