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

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

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