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.

Also known as: congenital bilateral absence of vas deferens, congenital bilateral aplasia of the vas deferens, vas deferens, congenital bilateral aplasia of, CAVD, CBAVD

0 clinical trials for this condition and its sub-types, 0 tagged with Congenital bilateral aplasia of vas deferens from CFTR mutation itself.