Disease #01565 (SCA2;ALS13 (ataxia, spinocerebellar, type 2 (SCA-2, sclerosis, lateral, amyotrophic (ALS-13))), OMIM:183090)

Official abbreviation SCA2;ALS13
Name ataxia, spinocerebellar, type 2 (SCA-2, sclerosis, lateral, amyotrophic (ALS-13))
OMIM ID 183090
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 ATXN2
Associated tissues -
Disease features -
Remarks -