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3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Cerebral sinovenous thrombosis
Hereditary angioedema type 1

F2 SERPING1
F5
PROZ


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
F2
(0.75)
SERPING1



Citations in the biomedical literature:


Cerebral sinovenous thrombosis
F2 F5 PROZ
Hereditary angioedema type 1
SERPING1



Cerebral sinovenous thrombosis
Hereditary angioedema type 1

Synonym(s):
- CSVT

Synonym(s):
- HAE-I
- Hereditary angioneurotic edema type 1

Classification (Orphanet):
- Rare neurologic disease
Classification (Orphanet):
- Rare allergic disease
- Rare genetic disease
- Rare systemic or rheumatologic disease

Classification (ICD10):
(no data available)
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: variable
Average age of death: -
Type of inheritance: autosomal dominant

External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: C538577

No signs/symptoms info available.