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 ×

F12-related hereditary angioedema with normal C1Inh

F12-related HAE with normal C1 inhibitor · HAE

ORPHA:100054

Acquired angioedema

AAE · Acquired C1 inhibitor deficiency

ORPHA:91385

Acquired angioedema type 1

Acquired angioneurotic edema type 1

ORPHA:100056

Acquired angioedema type 2

AAE 2 · AAE II

ORPHA:100055

Hereditary angioedema

Familial angioneurotic edema · HAE

ORPHA:91378

Non-histaminic angioedema

Angioneurotic edema · Bradykinine-induced angioedema

ORPHA:658

Renin-angiotensin-aldosterone system-blocker-induced angioedema

ACEI-related acquired angioedema · Acquired angioedema with normal C1INH

ORPHA:100057