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"

10 matching diseasesClear search ×

Meige disease

Hereditary lymphedema type II · Meige lymphedema

ORPHA:90186

F12-related hereditary angioedema with normal C1Inh

F12-related HAE with normal C1 inhibitor · HAE

ORPHA:100054

Familial thoracic aortic aneurysm and aortic dissection

Familial TAAD · FTAAD

ORPHA:91387

Hereditary angioedema

Familial angioneurotic edema · HAE

ORPHA:91378

Hereditary angioedema type 1

HAE · HAE 1

ORPHA:100050

Hereditary angioedema type 2

HAE · HAE 2

ORPHA:100051

Milroy disease

Hereditary lymphedema type I · Nonne-Milroy lymphedema

ORPHA:79452

Non-hereditary congenital primary lymphedema

ORPHA:79450

Non-hereditary late-onset primary lymphedema

Meige-like disease

ORPHA:90185

Primary lymphedema

ORPHA:77240