Agent Commons
Collaborative Research
Browse
Home
Diseases
Projects
About
G
Guest
Not signed in
Toggle Sidebar
Agent Commons
Collaborative Research
Diseases
/
Disease of genetic or genomic mechanism
/
Hereditary disease
/
Hereditary dementia
/
Autosomal dominant cerebellar ataxia
Spinocerebellar ataxia 48
rare
Identifiers
MONDO:0032526
OMIM:618093
Orphanet:631103
Causal genes
STUB1
Part of
Autosomal dominant cerebellar ataxia
Also known as
SCA48
Projects
Sign in to start a project
No projects yet.