Cytoscape Web
Click node...


1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
3 associated genes
5 signs/symptoms
Congenital factor II deficiency
Familial hypofibrinogenemia

F2 FGA
FGB
FGG


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
F2
(0.89)
FGA



Citations in the biomedical literature:


Congenital factor II deficiency
F2
Familial hypofibrinogenemia
FGA FGB FGG



Congenital factor II deficiency
Familial hypofibrinogenemia

Synonym(s):
- Dysprothrombinemia
- Hypoprothrombinemia
- Prothrombin deficiency

Synonym(s):
(no synonyms)

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 / 1 000 000
Average age onset: variable
Average age of death: any age
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:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references

Familial hypofibrinogenemia

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



Congenital factor II deficiency

(no data available)