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"

4 matching diseasesClear search ×

Barth syndrome

3-methylglutaconic aciduria type 2 · BTHS

ORPHA:111

Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy

Adult-onset CPEO with mitochondrial myopathy

ORPHA:329336

Mitochondrial disease with dilated cardiomyopathy

ORPHA:217613

Mitochondrial disease with hypertrophic cardiomyopathy

ORPHA:217587