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3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
3 associated genes
6 signs/symptoms
Cerebral sinovenous thrombosis
Familial dysfibrinogenemia

F2 FGA
F5 FGB
PROZ FGG


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
F2
(0.89)
FGA



Citations in the biomedical literature:


Cerebral sinovenous thrombosis
F2 F5 PROZ
Familial dysfibrinogenemia
FGA FGB FGG



Cerebral sinovenous thrombosis
Familial dysfibrinogenemia

Synonym(s):
- CSVT

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic 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 -
No MeSH references

Familial dysfibrinogenemia

Very frequent
- Autosomal dominant inheritance
- Epistaxis / nose bleeding
- Gastrointestinal bleeding / hemorrhage / hematemesis / melena / rectorrhagia
- Gingivorrhagia / gingival bleeding
- Hemorrhage / hemorrhagic syndrome / excessive / long-lasting bleeding

Frequent
- Venous thrombosis / phlebitis / thrombophlebitis



Cerebral sinovenous thrombosis

(no data available)