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Metadata
ID	DOID:0080288
Name	spinocerebellar ataxia 46
Definition	An autosomal dominant cerebellar ataxia that has_material_basis_in heterozygous mutation in the PLD3 gene on chromosome 19q13. https://pubmed.ncbi.nlm.nih.gov/29053796/
Xrefs	OMIM:617770
Parent Relationships	is_a autosomal dominant cerebellar ataxia