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 ×

Congenital retinal arteriovenous communication

Congenital arteriovenous anastomoses of the retina · Congenital arteriovenous communication of the retina

ORPHA:353334

Congenital renal artery stenosis

Congenital renovascular hypoplasia

ORPHA:97598

Hepatic arteriovenous malformation

Congenital hepatic arteriovenous malformation · HAVM

ORPHA:693846

Isolated retinal racemose hemangioma

RRH · Isolated retinal arteriovenous aneurysm 3

ORPHA:674924

OBSOLETE: Congenital arteriovenous fistula

ORPHA:98731

OBSOLETE: Congenital systemic arteriovenous fistula

ORPHA:2039

Peripheral congenital arteriovenous fistula

Peripheral congenital AVF

ORPHA:708051