Y-linked spermatogenic failure 2

Summary

DOID:0070187 - Y-linked spermatogenic failure 2

Disease Ontology Definition:A spermatogenic failure that is characterized by nonobstroctive azoospermia or oligozoospermia that has_material_basis_in interstitial deletions on the Yq11.221 chromosomal region.

Synonyms: SPGFY2, nonobstructive Y-linked spermatogenic failure,

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

: ddx3y

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010767 - spermatogenic failure, Y-linked, 2

MONDO:0010767 - spermatogenic failure, Y-linked, 2

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): Y-linked monogenic disease (is_a), spermatogenic failure (is_a)