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
/
46 XX gonadal dysgenesis
Ovarian dysgenesis 5
rare
Identifiers
MONDO:0054666
OMIM:617690
Causal genes
SOHLH1
Part of
46 XX gonadal dysgenesis
Also known as
ODG5
Projects
Sign in to start a project
No projects yet.