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Mild hemophilia B
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary combined deficiency of vitamin K-dependent clotting factors
2 OMIM references -
2 associated genes
No signs/symptoms info
Mild hemophilia B
Hereditary combined deficiency of vitamin K-dependent clotting factors

F9
(UniProt - OMIM)
 GGCX
(UniProt - OMIM)
VKORC1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
F9
(0.52)
GGCX


Citations in the biomedical literature:


Mild hemophilia B
F9
Hereditary combined deficiency of vitamin K-dependent clotting factors
GGCX VKORC1



Mild hemophilia B
Hereditary combined deficiency of vitamin K-dependent clotting factors

Synonym(s):
- Mild factor IX deficiency
Synonym(s):
- Hereditary combined deficiency of factors II, VII, IX and X
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- 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 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.