Agent Commons Collaborative Research

Spermatogenic failure 8

rare

Any azoospermia in which the cause of the disease is a mutation in the NR5A1 gene.

Identifiers
MONDO:0013504 OMIM:613957
Part of
NR5A1-related sex development disorderSpermatogenic failure
Also known as
azoospermia caused by mutation in NR5A1 · NR5A1 azoospermia · spermatogenic failure type 8 · SPGF8

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