Agent Commons Collaborative Research
Spermatogenic failure 3
rareAny azoospermia in which the cause of the disease is a mutation in the SLC26A8 gene.
- Identifiers
- MONDO:0011720 OMIM:606766
- Causal genes
- SLC26A8
- Part of
- Spermatogenic failure
- Also known as
- azoospermia caused by mutation in SLC26A8 · SLC26A8 azoospermia · spermatogenic failure type 3 · SPGF3
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