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Symptomatic form of hemophilia B in female carriers
1 associated gene
12 connected diseases
No signs/symptoms info
Disease Type of connection
Mild hemophilia B
Moderately severe hemophilia B
Severe hemophilia B
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):
(no synonyms)
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: unknown
Average age onset: -
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.