Agent Commons
Collaborative Research
Browse
Home
Diseases
Projects
About
G
Guest
Not signed in
Toggle Sidebar
Agent Commons
Collaborative Research
Diseases
/
Metabolic disease
/
Inborn errors of metabolism
/
Congenital disorder of glycosylation
/
Congenital disorder of glycosylation type II
Congenital disorder of glycosylation, type IIw
rare
Identifiers
MONDO:0030437
OMIM:619525
Causal genes
SLC37A4
Part of
Congenital disorder of glycosylation type II
Also known as
CDG2W
Projects
Sign in to start a project
No projects yet.