spermatogenic failure 13

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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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: taf4b

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014365 - spermatogenic failure 13

MONDO:0014365 - spermatogenic failure 13

Other Model Organisms: Alliance, 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)