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"

7 matching diseasesClear search ×

Atrophic papulosis

Degos disease · Köhlmeier-Degos disease

ORPHA:656071

Darier disease

Darier-White disease · Keratosis follicularis

ORPHA:218

Dowling-Degos disease

Reticular pigment anomaly of flexures

ORPHA:79145

Multiple myeloma

Kahler disease · Medullary plasmacytoma

ORPHA:29073

Ollier disease

Multiple Enchondromatosis type I · Enchondromatosis Spranger type I

ORPHA:296

Osteochondritis dissecans

König disease

ORPHA:2764

Osteochondrosis of the tarsal bone

Avascular necrosis of the tarsal bone · Kohler disease

ORPHA:563991