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Summary Literature (0)
DOID:0070178 - spermatogenic failure 10

Disease Ontology Definition:A spermatogenic failure that is characterized by defects in the annulus or the ring-like structure located at the distal end of the flagellar midpiece the autosomal dominant inheritance of that has_material_basis_in mutation in the SEPT12 gene on chromosome 16p13.

Synonyms: SPGF10, Spermatogenic failure with defective sperm annulus,

Xenbase Genes : septin12

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013901 - spermatogenic failure 10

Other Model Organisms: Alliance, 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)