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"

17 matching diseasesClear search ×

Tako-Tsubo cardiomyopathy

Ampulla cardiomyopathy · Apical ballooning syndrome

ORPHA:66529

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 restrictive cardiomyopathy

ORPHA:217635

Histiocytoid cardiomyopathy

Foamy myocardial transformation of infancy · Infantile cardiomyopathy with histiocytoid change

ORPHA:137675

Inherited arrhythmogenic cardiomyopathy

Arrhythmogenic cardiomyopathy · ACM

ORPHA:247

Leigh syndrome with cardiomyopathy

Cardiomyopathy with hypotonia due to cytochrome C oxidase deficiency · Cardiomyopathy with myopathy due to COX deficiency

ORPHA:70474

Microcephaly-cardiomyopathy syndrome

Winship-Viljoen-Leary syndrome

ORPHA:2515

Mitochondrial DNA-related cardiomyopathy and hearing loss

mtDNA-related cardiomyopathy and deafness · Maternally-inherited cardiomyopathy and deafness

ORPHA:1349

Non-familial restrictive cardiomyopathy

ORPHA:217720

Peripartum cardiomyopathy

Postpartum cardiomyopathy

ORPHA:563

Rare cardiomyopathy

ORPHA:167848

Rare hypertrophic cardiomyopathy

ORPHA:217569

Restrictive cardiomyopathy

ORPHA:217632

Unclassified cardiomyopathy

ORPHA:217678