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 ×

Multiple myeloma

Kahler disease · Medullary plasmacytoma

ORPHA:29073

Cutaneous mastocytoma

Cutaneous local mastocytoma · Multiple mastocytoma

ORPHA:79455

Familial keratoacanthoma

Hereditary keratoacanthoma · Multiple keratoacanthoma

ORPHA:493