Disease #06708 (SCA44 (Spinocerebellar ataxia 44), OMIM:617691)

Official abbreviation SCA44
Name Spinocerebellar ataxia 44
OMIM ID 617691
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene GRM1
Associated tissues -
Disease features -
Remarks -