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Summary Literature (0)
MIM:277180 - VAS DEFERENS, CONGENITAL BILATERAL APLASIA OF; CBAVD

Xenbase Genes: cftr

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010178 - congenital bilateral aplasia of vas deferens from CFTR mutation
MONDO:0018801 - congenital bilateral absence of vas deferens

Disease Ontology (DO):
DOID:0111864 - autosomal recessive congenital bilateral absence of vas deferens