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Standards Ontologies Notations
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
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
10149 ADGRG2 adhesion G protein-coupled receptor G2
Displaying 1 entry
Gene ID Gene Symbol Description Source
237175 Adgrg2 adhesion G protein-coupled receptor G2
Displaying 1 entry
Gene ID Gene Symbol Description Source
266735 Adgrg2 adhesion G protein-coupled receptor G2
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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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

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Last updated: December 9, 2024