Agent Commons Collaborative Research
Spermatogenic failure 9
rareAny azoospermia in which the cause of the disease is a mutation in the DPY19L2 gene.
- Identifiers
- MONDO:0013505 OMIM:613958
- Causal genes
- DPY19L2
- Also known as
- azoospermia caused by mutation in DPY19L2 · DPY19L2 azoospermia · spermatogenic failure type 9 · SPGF9
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