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Summary Literature (0)
DOID:0070182 - spermatogenic failure 13

Disease Ontology Definition:A spermatogenic failure that is characterized by autosomal recessive inheritance of azoospermia or oligozoospermia that has_material_basis_in mutation in the TAF4B gene on chromosome 18q11.

Synonyms: SPGF13,

Xenbase Genes : taf4b

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014365 - spermatogenic failure 13

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), spermatogenic failure (is_a)