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

MIM:277180

Ontology

Human Disease ( DOID:0111864 )

Relationships

is a type of: autosomal recessive disease congenital bilateral absence of vas deferens

autosomal recessive disease congenital bilateral absence of vas deferens Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models