SRY, sex determining region Y, 6736

N. diseases: 315; N. variants: 27
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0151721
Disease: Testicular hypogonadism
Testicular hypogonadism
0.110 GeneticVariation disease BEFREE Cytogenetic, molecular cytogenetic and molecular genetic studies indicated the derivative monocentric Y chromosome with duplication of Yp11 (including SRY gene) and partial deletion of Yq11 (including azoospermia factor - AZFb-c regions) as the most probable cause of the severe testicular failure. 17935509 2007
CUI: C0151721
Disease: Testicular hypogonadism
Testicular hypogonadism
0.110 Biomarker disease HPO