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 ×

Familial isolated restrictive cardiomyopathy

Familial or idiopathic restrictive cardiomyopathy

ORPHA:75249

Familial dilated cardiomyopathy

ORPHA:217607

Familial isolated dilated cardiomyopathy

Familial or idiopathic dilated cardiomyopathy

ORPHA:154

Familial restrictive cardiomyopathy

ORPHA:217635

Lysosomal disease with restrictive cardiomyopathy

ORPHA:217638

Non-familial dilated cardiomyopathy

ORPHA:217629

Non-familial hypertrophic cardiomyopathy

ORPHA:217598

Non-familial restrictive cardiomyopathy

ORPHA:217720

OBSOLETE: Familial restrictive cardiomyopathy type 1

ORPHA:99985

OBSOLETE: Familial restrictive cardiomyopathy type 2

ORPHA:99986

OBSOLETE: Familial restrictive cardiomyopathy type 3

OBSOLETE: RCM3

ORPHA:218432

Rare familial disorder with hypertrophic cardiomyopathy

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

ORPHA:99739

Restrictive cardiomyopathy

ORPHA:217632