Disease #02497 (SCA12 (ataxia, spinocerebellar, type 12 (SCA-12)), OMIM:604326)

Official abbreviation SCA12
Name ataxia, spinocerebellar, type 12 (SCA-12)
OMIM ID 604326
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene PPP2R2B
Associated tissues -
Disease features -
Remarks -