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"

17 matching diseasesClear search ×

Mucocutaneous venous malformations

Cutaneous and mucosal venous malformation · VMCM

ORPHA:2451

Brain arteriovenous malformation

Cerebral arteriovenous malformation

ORPHA:46724

Capillary malformation-arteriovenous malformation

CM-AVM

ORPHA:137667

Fast-flow vascular malformation

Rare arteriovenous malformation

ORPHA:211266

Gastrointestinal tract arteriovenous malformation

GI arteriovenous malformation · Angiodysplasia of the GI tract

ORPHA:693832

Glomuvenous malformation

Glomangiomatosis · Hereditary multiple glomangiomas

ORPHA:83454

Hepatic arteriovenous malformation

Congenital hepatic arteriovenous malformation · HAVM

ORPHA:693846

Hereditary neurocutaneous malformation

ORPHA:1062

Peripheral arteriovenous malformation

Peripheral AVM

ORPHA:708046

Peripheral fast-flow vascular malformation

Peripheral arteriovenous malformation

ORPHA:707944

Rare genetic venous malformation

ORPHA:459548

Renal arteriovenous malformation

rAVM · Arteriovenous malformation of the kidney

ORPHA:693839

Segmental venous malformation

Bockenheimer syndrome · Genuine diffuse phlebectasia

ORPHA:217008

Slow-flow malformation, venous type

Rare venous malformation

ORPHA:211252

Splenic venous malformation

Splenic cavernous malformation · Splenic slow flow venous malformation

ORPHA:688523

Uterine arteriovenous malformation

UAVM · Arteriovenous malformation of the uterus

ORPHA:693815

Visceral arteriovenous malformation

Arteriovenous malformation of internal organs

ORPHA:693855