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Standards Ontologies Notations
Guidelines
MIRAGE
X-linked congenital bilateral absence of vas deferens

Summary
Synonym
  • CBAVDX
Definition
A congenital bilateral absence of vas deferens that has_material_basis_in mutation in the ADGRG2 gene on chromosome Xp22.13.
Super Class
congenital bilateral absence of vas deferens
Disease Ontology
DOID:0111863
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
10149 ADGRG2 adhesion G protein-coupled receptor G2
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
Q8IZP9 Adhesion G-protein coupled receptor G2
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 8, 2025