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
/
Spermatogenic failure
Spermatogenic failure 30
rare
Identifiers
MONDO:0020851
OMIM:618110
Causal genes
TDRD9
Part of
Spermatogenic failure
Also known as
SPGF30
Projects
Sign in to start a project
No projects yet.