autosomal recessive congenital bilateral absence of vas deferens Disease Ontology Browser

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Disease Ontology Browser

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 the CFTR gene 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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