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 -
Phenotype entries for this disease -
Associated with 1 gene WWOX
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 11:00:40 +02:00 (CEST)
Date last edited N/A