Disease #05066 (SCAR-12 (ataxia, spinocerebellar, autosomal recessive, type 12 (SCAR12)), OMIM:614322)

Official abbreviation SCAR-12
Name ataxia, spinocerebellar, autosomal recessive, type 12 (SCAR12)
OMIM ID 614322
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene WWOX
Associated tissues -
Disease features -
Remarks -