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Summary Literature (0)
DOID:0070173 - spermatogenic failure 7

Disease Ontology Definition:A spermatogenic failure that is characterized by autosomal recessive inheritance of impaired or absent sperm motility and increased incidence of morphologically abnormal sperm that has_material_basis_in mutation in the CATSPER1 gene on chromosome 11q13.

Synonyms: SPGF7

Xenbase Genes : strc

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013070 - spermatogenic failure 7

MIM:
MIM:612997 - SPERMATOGENIC FAILURE 7; SPGF7

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)