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dilated cardiomyopathy 1D

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the TNNT2 gene.
Uniprot Description A disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death.
Mondo Term and Equivalent IDs
MONDO:0011095:  dilated cardiomyopathy 1D
MESH:C563306: 
UMLS:C1832243: