Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.100 GeneticVariation disease GWASDB Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. 18587394 2008
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.100 GeneticVariation disease GWASDB Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. 17804789 2007
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.010 GeneticVariation disease BEFREE Additionally, two haplotypes (TCTG, TCTA) were also significantly associated with SCZ. 26654950 2016
CUI: C0740394
Disease: Hyperuricemia
Hyperuricemia 		0.010 GeneticVariation disease BEFREE Alleles of the TCTA repeat in the 3rd intron of the HPRT gene were found to be associated with primary hyperuricemia; consequently, these alleles may be considered risk factors for primary hyperuricemia. 22194167 2011
CUI: C0023492
Disease: Leukemia, T-Cell
Leukemia, T-Cell 		0.010 GeneticVariation disease BEFREE T-cell leukemia translocation-associated gene (TCTA) protein is required for human osteoclastogenesis. 19560569 2009