AR, androgen receptor, 367

N. diseases: 854; N. variants: 163
Disease: Congenital hernia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0235832
Disease: Congenital hernia
Congenital hernia 		0.010 GeneticVariation disease BEFREE Androgen receptor genotypes encoding moderate functional variation may influence cryptorchidism risk, particularly among boys with bilateral nondescent or congenital hernia, and may explain in part the elevated risk of testicular seminoma experienced by ex-cryptorchid boys. 22188741 2012