Search Ontology:
Human Disease

X-linked congenital bilateral absence of vas deferens

Term ID
DOID:0111863
Synonyms
  • CBAVDX
Definition
A congenital bilateral absence of vas deferens that has_material_basis_in mutation in the ADGRG2 gene on chromosome Xp22.13. https://pubmed.ncbi.nlm.nih.gov/27476656/
References
Ontology
Human Disease   ( DOID:0111863 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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