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 28, autosomal recessive
Identifiers
MONDO:0030697
OMIM:619781
Causal genes
LOXL3
Part of
Myopia
Also known as
MYP28
Projects
Sign in to start a project
No projects yet.