Disease: Azoospermia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004509
Disease: Azoospermia
Azoospermia 		0.010 GeneticVariation disease BEFREE One intronic SNP in MLH1 (rs4647269) and two non-synonymous SNPs in PMS2 (rs1059060, Ser775Asn) and MSH5 (rs2075789, rs2075789;rs864622096;587781908;rs786203623;rs587781908;rs1248142939;s587781908" genes_norm="4292;4439;5395">Pro29Ser) seem to be risk factors for the development of azoospermia or oligozoospermia. 22594646 2012