Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.100 GeneticVariation phenotype GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
CUI: C0010495
Disease: Cutis Laxa
Cutis Laxa 		0.100 GeneticVariation disease CLINVAR
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum 		0.100 GeneticVariation disease CLINVAR
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		0.100 GeneticVariation disease CLINVAR
CUI: C0746102
Disease: Chronic lung disease
Chronic lung disease 		0.100 GeneticVariation disease CLINVAR
CUI: C1845847
Disease: Coarse facial features
Coarse facial features 		0.100 GeneticVariation phenotype CLINVAR
CUI: C4317146
Disease: Acid reflux
Acid reflux 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0041956
Disease: Ureteral obstruction
Ureteral obstruction 		0.010 AlteredExpression phenotype BEFREE Interestingly, the up-regulation of lncRNA Gm16076, Gm26669, and down-regulation of Fam120aos were highly correlated with the up-regulation of mRNA levels of fibrosis-related gene ITGB1, STAT3 and reduction of Pink1 in UUO kidney, respectively. 31104327 2019