Subtype of: Autosomal recessive ataxia · Spinocerebellar ataxia

Pathways column key: KEGG Reactome

Disease Term	Disease ID	Gene Symbol	Classification	References	Source	Pathways
spinocerebellar ataxia, autosomal recessive 27	EFO_0010248	GDAP2	Causal	38587696 30084953 37070050 32437512 32428220	ClinGen, Open Targets	—

Spinocerebellar ataxia, autosomal recessive 27