X-linked congenital bilateral absence of vas deferens Disease Ontology Browser

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Disease Ontology Browser

X-linked congenital bilateral absence of vas deferens (DOID:0111863)
Alliance: disease page
Synonyms: CBAVDX
Alt IDs: OMIM:300985
Definition: A congenital bilateral absence of vas deferens that has_material_basis_in mutation in the ADGRG2 gene on chromosome Xp22.13.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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