Rare Disease Library

Hereditary angioedema type 1

HAE · HAE 1

Acquired angioedema

AAE · Acquired C1 inhibitor deficiency

Acquired angioedema type 1

Acquired angioneurotic edema type 1

Acquired angioedema type 2

AAE 2 · AAE II

Charcot-Marie-Tooth disease type 1

Autosomal dominant demyelinating Charcot-Marie-Tooth disease · CMT1

Distal hereditary motor neuropathy type 1

Autosomal dominant distal juvenile spinal muscular atrophy type 1 · dHMN1

F12-related hereditary angioedema with normal C1Inh

F12-related HAE with normal C1 inhibitor · HAE

Hereditary angioedema

Familial angioneurotic edema · HAE

Hereditary angioedema type 2

HAE · HAE 2

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 1

HSAN1 · Hereditary sensory and autonomic neuropathy type I

Hereditary sensory and autonomic neuropathy type 1B

HSAN with cough and gastroesophageal reflux · HSAN1B

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