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dilated cardiomyopathy 1S | RareConnect | RareConnect.io

/left ventricular noncompaction

/familial isolated dilated cardiomyopathy

/dilated cardiomyopathy 1S

dilated cardiomyopathy 1S

Rare Disease

MONDO:0013262

Also Known As

CMD1SMYH7 familial isolated dilated cardiomyopathycardiomyopathy, dilated, type 1Sdilated cardiomyopathy type 1Sfamilial isolated dilated cardiomyopathy caused by mutation in MYH7cardiomyopathy, dilated, 1Sdilated cardiomyopathy-1Sleft ventricular noncompaction 5

Definition

Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the MYH7 gene.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:613426 ↗

GARD

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