Rare Disease Library

Familial isolated dilated cardiomyopathy

Familial or idiopathic dilated cardiomyopathy

Congenital disorder of glycosylation with dilated cardiomyopathy

CDG with dilated cardiomyopathy

Dilated cardiomyopathy

Dilated cardiomyopathy with ataxia

3-methylglutaconic aciduria type 5 · DCMA syndrome

Familial dilated cardiomyopathy

Familial dilated cardiomyopathy with conduction defect due to LMNA mutation

Familial idiopathic dilatation of the right atrium

Familial isolated restrictive cardiomyopathy

Familial or idiopathic restrictive cardiomyopathy

Familial restrictive cardiomyopathy

Kidney tubulopathy-dilated cardiomyopathy syndrome

Mitochondrial disease with dilated cardiomyopathy

Non-familial dilated cardiomyopathy

Non-familial hypertrophic cardiomyopathy

Non-familial rare disease with dilated cardiomyopathy

Non-familial restrictive cardiomyopathy

OBSOLETE: Familial restrictive cardiomyopathy type 1

OBSOLETE: Familial restrictive cardiomyopathy type 2

OBSOLETE: Familial restrictive cardiomyopathy type 3

OBSOLETE: RCM3

Rare familial disorder with hypertrophic cardiomyopathy

Rare familial disorder with hypertrophic obstructive cardiomyopathy · Rare familial disorder with hypertrophic subaortic stenosis

Sensorineural deafness with dilated cardiomyopathy

Neurosensory deafness with dilated cardiomyopathy · Neurosensory hearing loss with dilated cardiomyopathy

Severe dilated cardiomyopathy due to lamin A/C mutation

Severe dilated cardiomyopathy with or without myopathy

Syndrome associated with dilated cardiomyopathy