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spermatogenic failure 3

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any azoospermia in which the cause of the disease is a mutation in the SLC26A8 gene.
Uniprot Description A disorder characterized by primary infertility, sperm morphologic abnormalities, and moderate to severe asthenozoospermia, condition in which the percentage of progressively motile sperm is abnormally low.
Mondo Term and Equivalent IDs
MONDO:0011720:  spermatogenic failure 3
MESH:C564665: 
UMLS:C1847540: