Congenital bilateral aplasia of vas deferens from CFTR mutation
MONDO:0010178An 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
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Disease
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Hereditary disease
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Reproductive system disorder
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Human disease
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Male reproductive system disorder
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Disease of genetic or genomic mechanism
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CFTR-related disorder
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Congenital bilateral absence of vas deferens
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