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Congenital factor II deficiency
1 OMIM reference -
1 associated gene
43 connected diseases
No signs/symptoms info
Disease Type of connection
Cerebral sinovenous thrombosis
Fetal and neonatal alloimmune thrombocytopenia
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
Budd-Chiari syndrome
Congenital factor V deficiency
Congenital plasminogen activator inhibitor type 1 deficiency
East Texas bleeding disorder
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
Glanzmann thrombasthenia
Hereditary angioedema type 1
Hereditary angioedema type 2
Immunodeficiency due to an early component of complement deficiency
Congenital analbuminemia
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
Congenital factor XI deficiency
Congenital factor XIII deficiency
Congenital high-molecular-weight kininogen deficiency
Hereditary thrombophilia due to congenital protein C deficiency
Hereditary thrombophilia due to congenital protein S deficiency
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
Synonym(s):
- Dysprothrombinemia
- Hypoprothrombinemia
- Prothrombin deficiency
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: any age
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
F2 P00734176930
No signs/symptoms info available.