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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease congenital bilateral absence of vas deferens
Comorbidity C0010674|cystic fibrosis
Sentences 3
PubMedID- 20100616 Association of cystic fibrosis genetic modifiers with congenital bilateral absence of the vas deferens.
PubMedID- 22842702 However, the distribution of the cftr polymorphisms m470v, poly-t, tg-repeats and f508del mutation in the chinese cbavd population with presumed low cystic fibrosis (cf) frequency remains to be evaluated.
PubMedID- 25899114 Objectives: to review the management with assisted reproductive technologies (art) of men with congenital bilateral absence of vas deferens (cbavd), associated with cystic fibrosis or not, after surgical retrieval [epididymal aspiration (mesa) or testicular biopsy (tese)].

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