Genes | Associated disease | ICD –10 code | PMID | |
---|---|---|---|---|
Heart | MIF,CAV2,ACSS2,JARID2,FAM212B,FRMD4A,CHM,TRPM6,PDSS2,NFIA,HTR1D,HS6ST3,DIS3,PARP4,SOX6,DAAM2,DOPEY2,MYO5A,PLA2G4E,HDAC9,MYO1H,ABCB1,GREM1,RPS6KA5,HYOU1 | Coronary artery disease in patients with heart failure | I25* | 32,618,141 [33] |
ST6GALNAC1,HOXA5,EMP1,SULF1,NGEF,SOST,HOXD4,TM4SF1,PLG,TMCO5A,WT1,IKZF1,ALDH1A3,ALX4,THSD4,PAX9,CEP170,S100A10,RNF207,GLRX,SH2D2A,ESR1,ELANE | Coronary artery disease | I25* | 25,856,389 [22] | |
F2RL3, ABTB2 | Myocardial Infarction | I21.9 | ||
ADAMTS2 | Cardiac hypertrophy | I42.2 | 28,373,586 [116] | |
ZBTB20 | Cardiac remodeling | - | 33,063,955 [117] | |
Shared | C7orf50, FBXL13, PRKCZ, KCNQ1, THBS1, PRDM16, DNMT3A, HOXA, HOXC4, TNXB, HOXB3, PTPRN2, SHANK2 | Weight loss | R63. 4 | 25,651,499 [118] |
RUNX3, MYLK, GALNT2, TRAPPC9, PRDM16, NR2F2, HOXA3, HOXB3, AXIN2 | Congenital heart defects (CHD) | Q24.9 | ||
PTPRN2, TRAPPC9 | Incident coronary heart disease | I25.10 | 34,627,379 [121] | |
ACAP2 | Myocardial infarction | I21.9 | 34,139,744 [122] | |
Vasculature | CD4, CCR5, CD8A, CXCR3 | Chronic Chagasic Cardiomyopathy | B57. 2 | 31,087,713 [123] |
CD2, CCR5, CCR2, CD8A | Diabetes mellitus | E11.9 | 10,400,139 [124] | |
ARHGEF10 | Atherothrombotic stroke | I63.40 | 20,042,462 [125] | |
CAMTA1 | Cognitive function in adults with cardiovascular disease | - | 21,951,953 [126] | |
COL5A1 | Aortic dissection | I71. 010 | 34,041,919 [127] |