FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term autosomal recessive congenital bilateral absence of vas deferens ID (Ontology) DOID:0111864 (Human Disease)
Definition A congenital bilateral absence of vas deferens that has_material_basis_in homozygous or compound heterozygous mutation in the CFTR gene on chromosome 7q31.2.
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 Genes
 autosomal recessive congenital bilateral absence of vas deferens       3
 for disease ribbon | autosomal recessive congenital bilateral absence of vas deferens       3
 model of | autosomal recessive congenital bilateral absence of vas deferens       3
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X-linked monogenic disease
 |__congenital bilateral absence of vas deferens__
autosomal genetic disease                         |
 |__autosomal recessive disease___________________|
physical disorder                                 |
 |__congenital bilateral absence of vas deferens__|
male infertility                                  |
 |__congenital bilateral absence of vas deferens__|
                                                  autosomal recessive congenital bilateral absence of vas deferens  3 rec.
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Is a autosomal recessive disease
congenital bilateral absence of vas deferens
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MIM:277180