autosomal recessive congenital bilateral absence of vas deferens

Term ID

DOID:0111864

Synonyms

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. https://pubmed.ncbi.nlm.nih.gov/7529962/

References

• OMIM:277180

Ontology

Human Disease   ( DOID:0111864 )