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
/
Myopia
Myopia 11, autosomal dominant
Identifiers
MONDO:0012388
OMIM:609994
Part of
Myopia
Also known as
myopia 11 · MYP11
Projects
Sign in to start a project
No projects yet.