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spermatogenic failure 21

Disease Summary
Associated Targets (1)
Tchem

1


Uniprot Description An infertility disorder caused by spermatogenesis defects and characterized by acephalic spermatozoa in the semen of affected individuals. SPGF21 inheritance is autosomal recessive.
Mondo Term and Equivalent IDs
MONDO:0054725:  spermatogenic failure 21
UMLS:C4539991: