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Severe hemophilia B
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Mild hemophilia B
1 associated gene
No signs/symptoms info
Severe hemophilia B
Mild hemophilia B

F9
(UniProt - OMIM)
 F9
(UniProt - OMIM)

COMMON
GENES 		F9


Citations in the biomedical literature:


Severe hemophilia B
F9
Mild hemophilia B



Severe hemophilia B
Mild hemophilia B

Synonym(s):
- Severe factor IX deficiency
Synonym(s):
- Mild factor IX deficiency
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
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 -
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
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
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.