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autosomal recessive congenital bilateral absence of vas deferens (DOID:0111864)
Alliance: disease page
Alt IDs: OMIM:277180
Definition: A congenital bilateral absence of vas deferens that has_material_basis_in homozygous or compound heterozygous mutation in CFTR on chromosome 7q31.2.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
06/23/2022
MGI 6.20
The Jackson Laboratory