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Hereditary angioedema type 1
1 OMIM reference -
1 associated gene
11 connected diseases
No signs/symptoms info
Disease Type of connection
Immunodeficiency due to an early component of complement deficiency
Hereditary angioedema type 2
Cerebral sinovenous thrombosis
Congenital factor II deficiency
Craniofacial-ulnar-renal syndrome
Immunodeficiency due to MASP-2 deficiency
Congenital analbuminemia
Autosomal dominant severe congenital neutropenia
Cyclic neutropenia
Hypoplasminogenemia
Ligneous conjunctivitis
Synonym(s):
- HAE-I
- Hereditary angioneurotic edema type 1
Classification (Orphanet):
- Rare allergic disease
- Rare genetic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
1 MeSH reference: C538577
Gene symbol UniProt reference OMIM reference
SERPING1 P05155606860
No signs/symptoms info available.