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References OMIM Gene GeneReviews HGMD HGNC
GENATLAS PHENOTYPE
last update : 19-09-2016
Symbol CBAVDX
Location Xp22.13
Name X-Linked congenital bilateral absence of vas deferens
Corresponding gene ADGRG2
Main clinical features
  • Congenital bilateral aplasia of the vas deferens (CBAVD) leads to male infertility
  • often accompanied by renal maldevelopment
  • Genetic determination sex linked
    Function/system disorder sex-genitalia
    Type disease
    Remark(s)