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"

9 matching diseasesClear search ×

Peripartum cardiomyopathy

Postpartum cardiomyopathy

ORPHA:563

Congenital disorder of glycosylation with dilated cardiomyopathy

CDG with dilated cardiomyopathy

ORPHA:371176

Dilated cardiomyopathy

ORPHA:217604

Histiocytoid cardiomyopathy

Foamy myocardial transformation of infancy · Infantile cardiomyopathy with histiocytoid change

ORPHA:137675

Inherited arrhythmogenic cardiomyopathy

Arrhythmogenic cardiomyopathy · ACM

ORPHA:247

Rare cardiomyopathy

ORPHA:167848

Restrictive cardiomyopathy

ORPHA:217632

Tako-Tsubo cardiomyopathy

Ampulla cardiomyopathy · Apical ballooning syndrome

ORPHA:66529

Unclassified cardiomyopathy

ORPHA:217678