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"

4 matching diseasesClear search ×

Acquired angioedema

AAE · Acquired C1 inhibitor deficiency

ORPHA:91385

Acquired angioedema type 2

AAE 2 · AAE II

ORPHA:100055

Adenoid ameloblastoma

AA

ORPHA:689430

Autoimmune encephalitis

AE · AIE

ORPHA:622014