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dilated cardiomyopathy 3B | RareConnect | RareConnect.io

/neuromuscular disease caused by qualitative or quantitative defects of dystrophin

/hereditary neurological disease

/familial isolated dilated cardiomyopathy

/dilated cardiomyopathy 3B

dilated cardiomyopathy 3B

Rare Disease

MONDO:0010542

Also Known As

CMD3BDMD dilated cardiomyopathycardiomyopathy, dilated, type 3Bdilated cardiomyopathy 3Bdilated cardiomyopathy caused by mutation in DMDdilated cardiomyopathy type 3BDMD-related dilated cardiomyopathyX-linked dilated cardiomyopathycardiomyopathy, dilated, 3Bcardiomyopathy, dilated, X-linked

Definition

Any dilated cardiomyopathy in which the cause of the disease is a mutation in the DMD 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:302045 ↗

GARD

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