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
/
Fuchs' endothelial dystrophy
Corneal dystrophy, fuchs endothelial, 5
rare
Identifiers
MONDO:0013205
OMIM:613269
Part of
Fuchs' endothelial dystrophy
Also known as
FECD5
Projects
Sign in to start a project
No projects yet.