Search Ontology:
Human Disease
X-linked congenital bilateral absence of vas deferens
- Term ID
- DOID:0111863
- Synonyms
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- 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 )
- is a type of
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