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

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 afibrinogenemia
FGA FGB FGG



Cerebral sinovenous thrombosis
Familial afibrinogenemia

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: 1-9 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive

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

Familial afibrinogenemia

Very frequent
- Autosomal recessive inheritance
- Epistaxis / nose bleeding
- Gingivorrhagia / gingival bleeding
- Hemorrhage / hemorrhagic syndrome / excessive / long-lasting bleeding
- Hydrarthrosis / articular / joint effusion
- Metrorrhagia / menorrhagia / hemorrhagic cycles / hyper / poly / spanio / dysmenorrhea
- Spontaneous abortions

Occasional
- Intracranial / cerebral / meningeal hemorrhage


Cerebral sinovenous thrombosis

(no data available)