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
/
Cataract
Cataract 48
rare
Identifiers
MONDO:0032735
OMIM:618415
Causal genes
DNMBP
Part of
Cataract
Also known as
CTRCT48
Projects
Sign in to start a project
No projects yet.