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Disease association ontology term - MONDO:0013901 - spermatogenic failure 10

Term summary

ID
MONDO:0013901
Name
spermatogenic failure 10
Ontology or CV name
Disease association
Definition
Any azoospermia in which the cause of the disease is a mutation in the SEPT12 gene.

Parents

Annotation

Disease association

MONDO:0013901 - spermatogenic failure 10

References:

Genes: