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"

10 matching diseasesClear search ×

Familial intraosseous vascular malformation

Hereditary intraosseous vascular malformation · VMOS

ORPHA:140436

Familial cerebral cavernous malformation

Familial brain cavernous angioma · Familial cerebral cavernoma

ORPHA:221061

Fast-flow vascular malformation

Rare arteriovenous malformation

ORPHA:211266

Hereditary neurocutaneous malformation

ORPHA:1062

Neurovascular malformation

ORPHA:102006

Peripheral fast-flow vascular malformation

Peripheral arteriovenous malformation

ORPHA:707944

Rare combined vascular malformation

ORPHA:458837

Rare vascular malformation of major vessels

ORPHA:458844

Simple vascular malformation

ORPHA:211243

Uterine arteriovenous malformation

UAVM · Arteriovenous malformation of the uterus

ORPHA:693815