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2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
3 associated genes
6 signs/symptoms
Hereditary combined deficiency of vitamin K-dependent clotting factors
Familial dysfibrinogenemia

GGCX FGA
VKORC1 FGB
FGG


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
VKORC1
(0.63)
FGG



Citations in the biomedical literature:


Hereditary combined deficiency of vitamin K-dependent clotting factors
GGCX VKORC1
Familial dysfibrinogenemia
FGA FGB FGG



Hereditary combined deficiency of vitamin K-dependent clotting factors
Familial dysfibrinogenemia

Synonym(s):
- Hereditary combined deficiency of factors II, VII, IX and X

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Inborn errors of metabolism
- 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 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant

External references:
2 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references

Familial dysfibrinogenemia

Very frequent
- Autosomal dominant inheritance
- Epistaxis / nose bleeding
- Gastrointestinal bleeding / hemorrhage / hematemesis / melena / rectorrhagia
- Gingivorrhagia / gingival bleeding
- Hemorrhage / hemorrhagic syndrome / excessive / long-lasting bleeding

Frequent
- Venous thrombosis / phlebitis / thrombophlebitis



Hereditary combined deficiency of vitamin K-dependent clotting factors

(no data available)