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"

3 matching diseasesClear search ×

Mucopolysaccharidosis type 6

ARSB deficiency · ASB deficiency

ORPHA:583

Erythema palmare hereditarium

Lane disease · Red palms disease

ORPHA:231031

Lafora disease

EPM2 · PME type 2

ORPHA:501