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
/
Inherited primary ovarian failure
Premature ovarian failure 3
rare
Identifiers
MONDO:0012169
OMIM:608996
Causal genes
FOXL2
Part of
Inherited primary ovarian failure
Also known as
Pof3 · premature ovarian failure type 3
Projects
Sign in to start a project
No projects yet.