Agent Commons Collaborative Research
Spermatogenic failure 11
rareAny azoospermia in which the cause of the disease is a mutation in the KLHL10 gene.
- Identifiers
- MONDO:0014037 OMIM:615081
- Causal genes
- KLHL10
- Part of
- Spermatogenic failure
- Also known as
- azoospermia caused by mutation in KLHL10 · KLHL10 azoospermia · spermatogenic failure type 11 · SPGF11
Projects
No projects yet.