Rare Disease Library

Hereditary angioedema type 2

HAE · HAE 2

Acquired angioedema

AAE · Acquired C1 inhibitor deficiency

Acquired angioedema type 1

Acquired angioneurotic edema type 1

Acquired angioedema type 2

AAE 2 · AAE II

Autosomal dominant Charcot-Marie-Tooth disease type 2

Autosomal dominant axonal Charcot-Marie-Tooth disease · CMT2

Distal hereditary motor neuropathy type 2

Distal spinal muscular atrophy type 2 · dHMN2

F12-related hereditary angioedema with normal C1Inh

F12-related HAE with normal C1 inhibitor · HAE

Hereditary angioedema

Familial angioneurotic edema · HAE

Hereditary angioedema type 1

HAE · HAE 1

Hereditary angioedema with C1Inh deficiency

HAE · HAE with C1 inhibitor deficiency

Hereditary angioedema with normal C1Inh

HAE · HAE with normal C1 inhibitor

Hereditary sensory and autonomic neuropathy type 2

Autosomal recessive sensory radicular neuropathy · HSAN2

Meige disease

Hereditary lymphedema type II · Meige lymphedema

Milroy disease

Hereditary lymphedema type I · Nonne-Milroy lymphedema

Non-histaminic angioedema

Angioneurotic edema · Bradykinine-induced angioedema