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: nonobstructive Y-linked spermatogenic failure, SPGFY2

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

MIM:

MIM:415000 - SPERMATOGENIC FAILURE, Y-LINKED, 2; SPGFY2

MIM:415000 - SPERMATOGENIC FAILURE, Y-LINKED, 2; SPGFY2

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

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

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