TNNT2, troponin T2, cardiac type, 7139

N. diseases: 79; N. variants: 73
Disease: Left ventricular noncompaction ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1960469
Disease: Left ventricular noncompaction
Left ventricular noncompaction 		0.310 GermlineCausalMutation disease ORPHANET Severe familial left ventricular non-compaction cardiomyopathy due to a novel troponin T (TNNT2) mutation. 20083571 2010
CUI: C1960469
Disease: Left ventricular noncompaction
Left ventricular noncompaction 		0.310 GeneticVariation disease BEFREE Recently, mutations in myosin heavy chain (MYH7), cardiac actin (ACTC), and troponin T (TNNT2) were associated with left ventricular noncompaction, a form of cardiomyopathy characterized with hypertrabeculation that may also include reduced function of the left ventricle. 20031619 2009