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Summary Literature (0)
DOID:0070180 - spermatogenic failure 11


Disease Ontology Definition:A spermatogenic failure that is characterized by autosomal dominant inheritance of oligozoospermia and in some cases teratozoospermia and/or moderate asthenozoospermia that has_material_basis_in mutation in the KLHL10 gene on chromosome 17q21.

Synonyms: SPGF11,

Xenbase Genes : klhl10

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014037 - spermatogenic failure 11


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

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