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

GeneID	Gene_Symbol	DisGeNet_diseaseID	Disease_name	DisGeNet score	DisGeNet_sourceDB
7139	TNNT2	C1832243	CARDIOMYOPATHY, DILATED, 1D (disorder)	0.48	CTD_human;MGD;UNIPROT
7139	TNNT2	C1861864	Cardiomyopathy, Familial Hypertrophic, 2	0.48	CTD_human;MGD;UNIPROT
7139	TNNT2	C0007194	Hypertrophic Cardiomyopathy	0.438811308291123	BEFREE;CTD_human;GAD;HPO;LHGDN
7139	TNNT2	C0878544	Cardiomyopathies	0.426593983448111	BEFREE;CTD_human;GAD;HPO;LHGDN
7139	TNNT2	C0007193	Cardiomyopathy, Dilated	0.414507683674358	BEFREE;CTD_human;GAD;HPO
7139	TNNT2	C0018801	Heart failure	0.400549453568426	BEFREE;CTD_human;HPO
7139	TNNT2	C0949658	Cardiomyopathy, Hypertrophic, Familial	0.215862376597774	BEFREE;CTD_human;LHGDN
7139	TNNT2	C0018800	Cardiomegaly	0.205139940988102	CTD_human;GAD;LHGDN
7139	TNNT2	C0085298	Sudden Cardiac Death	0.204814057046576	CTD_human;GAD
7139	TNNT2	C0024117	Chronic Obstructive Airway Disease	0.202732912464814	CTD_human;LHGDN
7139	TNNT2	C0042514	Tachycardia, Ventricular	0.202407028523288	CTD_human;GAD
7139	TNNT2	C0018799	Heart Diseases	0.200549453568426	BEFREE;CTD_human
7139	TNNT2	C0018802	Congestive heart failure	0.200549453568426	BEFREE;HPO
7139	TNNT2	C0948089	Acute Coronary Syndrome	0.200274726784213	BEFREE;CTD_human
7139	TNNT2	C1960469	Left ventricular noncompaction	0.200274726784213	BEFREE;ORPHANET
7139	TNNT2	C0007222	Cardiovascular Diseases	0.2	CTD_human
7139	TNNT2	C0011071	Sudden death	0.2	HPO
7139	TNNT2	C0027540	Necrosis	0.2	CTD_human
7139	TNNT2	C0035220	Respiratory Distress Syndrome, Newborn	0.2	CTD_human
7139	TNNT2	C0151744	Myocardial Ischemia	0.2	CTD_human
7139	TNNT2	C0242698	Ventricular Dysfunction, Left	0.2	CTD_human
7139	TNNT2	C0348616	Other restrictive cardiomyopathy	0.2	ORPHANET
7139	TNNT2	C2676271	CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)	0.2	CTD_human
7139	TNNT2	C3715165	LEFT VENTRICULAR NONCOMPACTION 10	0.2	ORPHANET
7139	TNNT2	C3809288	LEFT VENTRICULAR NONCOMPACTION 8	0.2	ORPHANET
7139	TNNT2	C0027051	Myocardial Infarction	0.0166722015730956	BEFREE;LHGDN
7139	TNNT2	C0149721	Left Ventricular Hypertrophy	0.0159692765327315	BEFREE;GAD;LHGDN
7139	TNNT2	C1449563	Cardiomyopathy, Familial Idiopathic	0.0072865981044939	BEFREE;GAD
7139	TNNT2	C0016719	Friedreich Ataxia	0.00300763924902685	BEFREE;LHGDN
7139	TNNT2	C0004153	Atherosclerosis	0.00273291246481375	LHGDN
7139	TNNT2	C0007196	Restrictive cardiomyopathy	0.00273291246481375	LHGDN
7139	TNNT2	C0038454	Cerebrovascular accident	0.00273291246481375	LHGDN
7139	TNNT2	C1956346	Coronary Artery Disease	0.00273291246481375	LHGDN
7139	TNNT2	C1383860	Cardiac Hypertrophy	0.002407028523288	GAD
7139	TNNT2	C0340427	Familial dilated cardiomyopathy	0.0008241803526393	BEFREE
7139	TNNT2	C0745103	Hyperlipoproteinemia Type IIa	0.0005494535684262	BEFREE
7139	TNNT2	C0003507	Aortic Valve Stenosis	0.0002747267842131	BEFREE
7139	TNNT2	C0008031	Chest Pain	0.0002747267842131	BEFREE
7139	TNNT2	C0015230	Exanthema	0.0002747267842131	BEFREE
7139	TNNT2	C0085612	Ventricular arrhythmia	0.0002747267842131	BEFREE
7139	TNNT2	C0152101	Hypoplastic Left Heart Syndrome	0.0002747267842131	BEFREE
7139	TNNT2	C0349782	Ischemic cardiomyopathy	0.0002747267842131	BEFREE
7139	TNNT2	C0741923	cardiac event	0.0002747267842131	BEFREE
7139	TNNT2	C0848332	Spots on skin	0.0002747267842131	BEFREE
7139	TNNT2	C1841658	Progressive Familial Heart Block, Type II	0.0002747267842131	BEFREE
7139	TNNT2	C3887505	DYSFUNCTION - SKIN DISORDERS	0.0002747267842131	BEFREE
7139	TNNT2	C4021133	Left Ventricular Non-Compaction Syndrome	0.0002747267842131	BEFREE