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Cerebral sinovenous thrombosis
3 associated genes
50 connected diseases
No signs/symptoms info
Disease Type of connection
Congenital factor II deficiency
Budd-Chiari syndrome
Congenital factor V deficiency
East Texas bleeding disorder
Fetal and neonatal alloimmune thrombocytopenia
Hereditary thrombophilia due to congenital protein S deficiency
Hereditary thrombophilia due to congenital protein C deficiency
Atypical hemolytic uremic syndrome with thrombomodulin anomaly
Familial thrombomodulin anomalies
Familial afibrinogenemia
Familial dysfibrinogenemia
Familial hypodysfibrinogenemia
Familial hypofibrinogenemia
Familial renal amyloidosis due to fibrinogen A alpha-chain variant
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Congenital plasminogen activator inhibitor type 1 deficiency
Bernard-Soulier syndrome
Hereditary thrombophilia due to congenital antithrombin deficiency
Von Willebrand disease, platelet type
Mild hemophilia A
Moderately severe hemophilia A
Severe hemophilia A
Symptomatic form of hemophilia A in female carriers
Autosomal dominant macrothrombocytopenia
Congenital factor X deficiency
Glanzmann thrombasthenia
Hereditary angioedema type 1
Hereditary angioedema type 2
Immunodeficiency due to an early component of complement deficiency
Essential thrombocythemia
Myelofibrosis with myeloid metaplasia
Congenital analbuminemia
B-cell chronic lymphocytic leukemia
Fibronectin glomerulopathy
Myxoid / round cell liposarcoma
Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency
Hereditary combined deficiency of vitamin K-dependent clotting factors
Quebec platelet disorder
Alpha-1-antichymotrypsin deficiency
Autosomal dominant severe congenital neutropenia
Congenital factor XI deficiency
Congenital factor XIII deficiency
Congenital high-molecular-weight kininogen deficiency
Cyclic neutropenia
Immunodeficiency due to a late component of complements deficiency
Mild hemophilia B
Moderately severe hemophilia B
Pediatric systemic lupus erythematosus
Severe hemophilia B
Symptomatic form of hemophilia B in female carriers

Classification (Orphanet):
- Rare neurologic disease

Classification (ICD10):
(no data available)

Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references

Gene symbol UniProt reference OMIM reference
F2 P00734176930
F5 P12259612309
PROZ P22891176895
No signs/symptoms info available.