X-linked congenital bilateral absence of vas deferens

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Summary

Literature (0)

DOID:0111863 - X-linked congenital bilateral absence of vas deferens

Disease Ontology Definition:A congenital bilateral absence of vas deferens that has_material_basis_in mutation in the ADGRG2 gene on chromosome Xp22.13.

Synonyms: CBAVDX

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

: adgrg2

MIM:

MIM:300985 - VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF, X-LINKED; CBAVDX

MIM:300985 - VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF, X-LINKED; CBAVDX

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

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

Parent(s): congenital bilateral absence of vas deferens (is_a)