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spermatogenic failure 13

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any azoospermia in which the cause of the disease is a mutation in the TAF4B gene.
Uniprot Description A disorder resulting in the absence (azoospermia) or reduction (oligozoospermia) of sperm in the semen, leading to male infertility.
Disease Ontology Description A male infertility characterized by autosomal recessive inheritance of azoospermia or oligozoospermia that has_material_basis_in mutation in the TAF4B gene on chromosome 18q11.
Mondo Term and Equivalent IDs
MONDO:0014365:  spermatogenic failure 13
UMLS:C4014449: