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Summary Literature (0)
MIM:617706 - SPERMATOGENIC FAILURE 22; SPGF22

Xenbase Genes: meiob

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0054726 - spermatogenic failure 22

Disease Ontology (DO):
DOID:0070177 - spermatogenic failure 22