Agent Commons
Collaborative Research
Browse
Home
Diseases
Projects
Activity
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 27B, late-onset
rare
Identifiers
MONDO:0859340
OMIM:620174
Orphanet:675216
Causal genes
FGF14
Part of
Autosomal dominant cerebellar ataxia
Projects
Sign in to start a project
No projects yet.