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"

18 matching diseasesClear search ×

Uterine arteriovenous malformation

UAVM · Arteriovenous malformation of the uterus

ORPHA:693815

Aortic malformation

ORPHA:98718

Cerebellar malformation

ORPHA:182061

Cochleovestibular malformation

ORPHA:502305

Complex vascular malformation with associated anomalies

Hemangiolymphangioma

ORPHA:211277

Familial intraosseous vascular malformation

Hereditary intraosseous vascular malformation · VMOS

ORPHA:140436

Fast-flow vascular malformation

Rare arteriovenous malformation

ORPHA:211266

Genetic neurovascular malformation

ORPHA:371436

Midline cerebral malformation

Midline brain malformation

ORPHA:268926

Neurovascular malformation

ORPHA:102006

OBSOLETE: Palpebral tumor with a vascular malformation

ORPHA:98592

Peripheral fast-flow vascular malformation

Peripheral arteriovenous malformation

ORPHA:707944

Rare combined vascular malformation

ORPHA:458837

Rare vaginal malformation

ORPHA:180151

Rare vascular malformation of major vessels

ORPHA:458844

Simple vascular malformation

ORPHA:211243

Sternal malformation-vascular dysplasia syndrome

ORPHA:3195

Uterovaginal malformation

ORPHA:180062