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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
Echinobase Genes

MIM:615841 - spermatogenic failure 13; spgf13 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee