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Congenital factor XII deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Hereditary angioedema type 3
1 OMIM reference -
1 associated gene
No signs/symptoms info
Congenital factor XII deficiency
Hereditary angioedema type 3

F12
(UniProt - OMIM)
 F12
(UniProt - OMIM)

COMMON
GENES 		F12


Citations in the biomedical literature:


Congenital factor XII deficiency
F12
Hereditary angioedema type 3



Congenital factor XII deficiency
Hereditary angioedema type 3

Synonym(s):
- Congenital Hageman factor deficiency
Synonym(s):
- HAE 3
- HAE-III
- Hereditary angioneurotic edema type 3
- Inherited estrogen-associated angioedema
- Inherited estrogen-associated angioneurotic edema
- Inherited estrogen-dependent angioedema
- Inherited estrogen-dependent angioneurotic edema
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
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 -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D056828
No signs/symptoms info available.