spermatogenic failure 10

Summary

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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: septin12

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013901 - spermatogenic failure 10

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)