Source: ORPHANET

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7139
Gene Symbol: TNNT2
TNNT2
CUI: C0348616
Disease: Other restrictive cardiomyopathy
Other restrictive cardiomyopathy 		0.300 GermlineCausalMutation ORPHANET Infantile restrictive cardiomyopathy resulting from a mutation in the cardiac troponin T gene. 16651346

2006