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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

MIM:
MIM:615081 - SPERMATOGENIC FAILURE 11; SPGF11

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

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