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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

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