Cytoscape Web
Click node...

Mild hemophilia B
1 associated gene
12 connected diseases
No signs/symptoms info
Disease Type of connection
Moderately severe hemophilia B
Severe hemophilia B
Symptomatic form of hemophilia B in female carriers
Mild hemophilia A
Moderately severe hemophilia A
Severe hemophilia A
Symptomatic form of hemophilia A in female carriers
Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency
Cerebral sinovenous thrombosis
Congenital factor II deficiency
Congenital factor VII deficiency
Hereditary combined deficiency of vitamin K-dependent clotting factors
Synonym(s):
- Mild factor IX 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 / 1 000 000
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
F9 P00740300746
No signs/symptoms info available.