Disease #06331 (SCA42 (Spinocerebellar ataxia 42), OMIM:616795)

Official abbreviation SCA42
Name Spinocerebellar ataxia 42
OMIM ID 616795
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene CACNA1G
Associated tissues -
Disease features -
Remarks -