* We recommend a score >= 0.08 for meaningful Gene-Disease associations

GeneID Gene_Symbol DisGeNet_diseaseID Disease_name DisGeNet score DisGeNet_sourceDB
7137TNNI3C0007193Cardiomyopathy, Dilated0.418222833584082BEFREE;CTD_human;GAD;HPO
7137TNNI3C0007196Restrictive cardiomyopathy0.413627760544073BEFREE;CTD_human;GAD;HPO;LHGDN
7137TNNI3C0878544Cardiomyopathies0.408971760589768BEFREE;CTD_human;GAD;HPO;LHGDN
7137TNNI3C1861861CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)0.401923087489492BEFREE;CTD_human;UNIPROT
7137TNNI3C1860752CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 70.4CTD_human;UNIPROT
7137TNNI3C2678474CARDIOMYOPATHY, DILATED, 2A (disorder)0.4CTD_human;UNIPROT
7137TNNI3C2750091Cardiomyopathy, Dilated, 1FF0.4CTD_human;UNIPROT
7137TNNI3C0949658Cardiomyopathy, Hypertrophic, Familial0.2166353997931BEFREE;CTD_human;GAD;LHGDN
7137TNNI3C0027051Myocardial Infarction0.206015278498054BEFREE;CTD_human;LHGDN
7137TNNI3C0948089Acute Coronary Syndrome0.205465824929628CTD_human;LHGDN
7137TNNI3C0018799Heart Diseases0.200549453568426BEFREE;CTD_human
7137TNNI3C0018801Heart failure0.200549453568426BEFREE;HPO
7137TNNI3C0018802Congestive heart failure0.200549453568426BEFREE;HPO
7137TNNI3C0340279Ventricular hypertrophy0.200274726784213BEFREE;HPO
7137TNNI3C0348616Other restrictive cardiomyopathy0.2ORPHANET
7137TNNI3C3278923Dilated ventricles (finding)0.2HPO
7137TNNI3C3554568Young adult onset0.2HPO
7137TNNI3C3715165LEFT VENTRICULAR NONCOMPACTION 100.2ORPHANET
7137TNNI3C3809288LEFT VENTRICULAR NONCOMPACTION 80.2ORPHANET
7137TNNI3C4020899Autosomal recessive predisposition0.2HPO
7137TNNI3C0007194Hypertrophic Cardiomyopathy0.0415953779132494BEFREE;GAD;LHGDN
7137TNNI3C0018800Cardiomegaly0.0078728534529155GAD;LHGDN
7137TNNI3C0149721Left Ventricular Hypertrophy0.0053635106150022BEFREE;GAD
7137TNNI3C0085298Sudden Cardiac Death0.004814057046576GAD
7137TNNI3C1449563Cardiomyopathy, Familial Idiopathic0.0037806624443535BEFREE;GAD
7137TNNI3C0206146Myocardial Stunning0.00328236603323995BEFREE;LHGDN
7137TNNI3C0022661Kidney Failure, Chronic0.00300763924902685BEFREE;LHGDN
7137TNNI3C0034065Pulmonary Embolism0.00300763924902685BEFREE;LHGDN
7137TNNI3C0038454Cerebrovascular accident0.00300763924902685BEFREE;LHGDN
7137TNNI3C0002965Angina, Unstable0.00273291246481375LHGDN
7137TNNI3C0011880Diabetic Ketoacidosis0.00273291246481375LHGDN
7137TNNI3C0002395Alzheimer's Disease0.002407028523288GAD
7137TNNI3C0042514Tachycardia, Ventricular0.002407028523288GAD
7137TNNI3C1383860Cardiac Hypertrophy0.002407028523288GAD
7137TNNI3C3887505DYSFUNCTION - SKIN DISORDERS0.0016483607052786BEFREE
7137TNNI3C0745103Hyperlipoproteinemia Type IIa0.0008241803526393BEFREE
7137TNNI3C0004238Atrial Fibrillation0.0005494535684262BEFREE
7137TNNI3C0011570Mental Depression0.0005494535684262BEFREE
7137TNNI3C0011581Depressive disorder0.0005494535684262BEFREE
7137TNNI3C0149978Adenocarcinoma of rectum0.0005494535684262BEFREE
7137TNNI3C0003507Aortic Valve Stenosis0.0002747267842131BEFREE
7137TNNI3C0007113Rectal Carcinoma0.0002747267842131BEFREE
7137TNNI3C0007222Cardiovascular Diseases0.0002747267842131BEFREE
7137TNNI3C0008626Congenital chromosomal disease0.0002747267842131BEFREE
7137TNNI3C0009402Colorectal Carcinoma0.0002747267842131BEFREE
7137TNNI3C0013264Muscular Dystrophy, Duchenne0.0002747267842131BEFREE
7137TNNI3C0015672Fatigue0.0002747267842131BEFREE
7137TNNI3C0026848Myopathy0.0002747267842131BEFREE
7137TNNI3C0027059Myocarditis0.0002747267842131BEFREE
7137TNNI3C0155626Acute myocardial infarction0.0002747267842131BEFREE
7137TNNI3C0276138Viral myocarditis0.0002747267842131BEFREE
7137TNNI3C0349782Ischemic cardiomyopathy0.0002747267842131BEFREE
7137TNNI3C0494165Secondary malignant neoplasm of liver0.0002747267842131BEFREE
7137TNNI3C0700323Observation of Neuromuscular Block0.0002747267842131BEFREE
7137TNNI3C0741923cardiac event0.0002747267842131BEFREE
7137TNNI3C2316810Chronic kidney disease stage 50.0002747267842131BEFREE
7137TNNI3C2584778Thrombotic thrombocytopenic purpura, acquired0.0002747267842131BEFREE
7137TNNI3C2717961Thrombotic Microangiopathies0.0002747267842131BEFREE