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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Congenital factor II deficiency
Von Willebrand disease, platelet type

F2 GP1BA


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
F2
(0.84)
GP1BA



Citations in the biomedical literature:


Congenital factor II deficiency
F2
Von Willebrand disease, platelet type
GP1BA



Congenital factor II deficiency
Von Willebrand disease, platelet type

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

Synonym(s):
- PT-VWD
- Pseudo-Von Willebrand disease
- Pseudo-Von Willebrand disease type 2B

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: -
Average age onset: -
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

No signs/symptoms info available.