FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term X-linked congenital bilateral absence of vas deferens ID (Ontology) DOID:0111863 (Human Disease)
Definition A congenital bilateral absence of vas deferens that has_material_basis_in mutation in the ADGRG2 gene on chromosome Xp22.13.
Also Known As "CBAVDX"
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 Genes
 X-linked congenital bilateral absence of vas deferens       2
 for disease ribbon | X-linked congenital bilateral absence of vas deferens       2
 model of | X-linked congenital bilateral absence of vas deferens       2
Spanning Tree (Parents/Children)
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X-linked monogenic disease__
physical disorder___________|
male infertility____________|
                            congenital bilateral absence of vas deferens
                             |__X-linked congenital bilateral absence of vas deferens  2 rec.
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Is a congenital bilateral absence of vas deferens
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Synonyms
  • "CBAVDX" EXACT OMO:0003012
Secondary IDs
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MIM:300985