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Summary Literature (0)
DOID:0070181 - spermatogenic failure 23

Disease Ontology Definition:A spermatogenic failure that is characterized by autosomal recessive inhertitance of nonobstructive azoospermia that has_material_basis_in mutation in the TEX14 gene on chromosome 17q23.

Synonyms: SPGF23

Xenbase Genes : tex14


MIM:
MIM:617707 - SPERMATOGENIC FAILURE 23; SPGF23

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)