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"

5 matching diseasesClear search ×

Retinal capillary malformation

Retinal cavernous hemangioma

ORPHA:71213

Familial cerebral cavernous malformation

Familial brain cavernous angioma · Familial cerebral cavernoma

ORPHA:221061

Isolated retinal racemose hemangioma

RRH · Isolated retinal arteriovenous aneurysm 3

ORPHA:674924

Macrocystic lymphatic malformation

Cavernous lymphangioma · Cavernous lymphatic malformation

ORPHA:79489

Verrucous hemangioma

ORPHA:464318