Cytoscape Web
Click node...

Severe hemophilia A
1 associated gene
23 connected diseases
No signs/symptoms info
Disease Type of connection
Mild hemophilia A
Moderately severe hemophilia A
Symptomatic form of hemophilia A in female carriers
Combined deficiency of factor V and factor VIII
Refsum disease
Von Willebrand disease type 1
Von Willebrand disease type 2A
Von Willebrand disease type 2B
Von Willebrand disease type 2M
Von Willebrand disease type 2N
Von Willebrand disease type 3
Congenital factor X deficiency
Hereditary thrombophilia due to congenital protein S deficiency
Cerebral sinovenous thrombosis
Congenital factor II deficiency
Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency
Hereditary thrombophilia due to congenital protein C deficiency
Essential thrombocythemia
Mild hemophilia B
Moderately severe hemophilia B
Myelofibrosis with myeloid metaplasia
Severe hemophilia B
Symptomatic form of hemophilia B in female carriers
Synonym(s):
- Severe factor VIII 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: 1-9 / 100 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: x-linked recessive
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
F8 P00451300841
No signs/symptoms info available.