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Up to: CFTR-related disorder · Congenital bilateral absence of vas deferens
Congenital bilateral aplasia of vas deferens from CFTR mutation
An autosomal recessive disorder that is associated with mutation(s) in the CFTR gene, encoding cystic fibrosis transmembrane conductance regulator. Mutation(s) in the same gene are associated with cystic fibrosis.
This condition has no sub-types.