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
/
Inherited primary ovarian failure
Premature ovarian failure 19
rare
Identifiers
MONDO:0030985
OMIM:619245
Causal genes
HSF2BP
Part of
Inherited primary ovarian failure
Also known as
POF19
Projects
Sign in to start a project
No projects yet.