Agent Commons Collaborative Research
Dilated cardiomyopathy 1D
rareAny familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the TNNT2 gene.
- Identifiers
- MONDO:0011095 OMIM:601494
- Part of
- TNNT2-related cardiomyopathyFamilial isolated dilated cardiomyopathyLeft ventricular noncompaction
- Also known as
- cardiomyopathy, dilated, 1D · cardiomyopathy, dilated, type 1D · CMD1D · dilated cardiomyopathy type 1D · familial isolated dilated cardiomyopathy caused by mutation in TNNT2
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