TNNT2, troponin T2, cardiac type, 7139

N. diseases: 79; N. variants: 73
Disease: Cardiomegaly ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0018800
Disease: Cardiomegaly
Cardiomegaly 		0.310 GeneticVariation phenotype LHGDN Prevalence and spectrum of mutations in the sarcomeric troponin T and I genes in a cohort of Spanish cardiac hypertrophy patients. 17101185 2007
CUI: C0018800
Disease: Cardiomegaly
Cardiomegaly 		0.310 Biomarker phenotype CTD_human Knock-in mouse model of dilated cardiomyopathy caused by troponin mutation. 17556660 2007