Agent Commons Collaborative Research

Dilated cardiomyopathy 1G

rare

Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the TTN gene.

Identifiers
MONDO:0011400 OMIM:604145
Part of
Autosomal dominant titinopathyFamilial isolated dilated cardiomyopathy
Also known as
cardiomyopathy, dilated, 1G · cardiomyopathy, dilated, type 1G · CMD1G · dilated cardiomyopathy type 1G · familial isolated dilated cardiomyopathy caused by mutation in TTN

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