Rare Disease Library

Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.

Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"

13 matching diseasesClear search ×

Isolated atrial standstill

Isolated atrial cardiomyopathy with heart block

ORPHA:1344

Congenital disorder of glycosylation with dilated cardiomyopathy

CDG with dilated cardiomyopathy

ORPHA:371176

Dilated cardiomyopathy

ORPHA:217604

Dilated cardiomyopathy with ataxia

3-methylglutaconic aciduria type 5 · DCMA syndrome

ORPHA:66634

Familial dilated cardiomyopathy

ORPHA:217607

Familial isolated dilated cardiomyopathy

Familial or idiopathic dilated cardiomyopathy

ORPHA:154

Familial isolated restrictive cardiomyopathy

Familial or idiopathic restrictive cardiomyopathy

ORPHA:75249

Inherited isolated arrhythmogenic cardiomyopathy

ORPHA:217656

Mitochondrial disease with dilated cardiomyopathy

ORPHA:217613

Non-familial rare disease with dilated cardiomyopathy

ORPHA:324767

Sensorineural deafness with dilated cardiomyopathy

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

ORPHA:217622

Severe dilated cardiomyopathy due to lamin A/C mutation

Severe dilated cardiomyopathy with or without myopathy

ORPHA:83618

Syndrome associated with dilated cardiomyopathy

ORPHA:217619