Cytoscape Web
Click node...

Cerebral sinovenous thrombosis
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Von Willebrand disease, platelet type
1 OMIM reference -
1 associated gene
No signs/symptoms info
Cerebral sinovenous thrombosis
Von Willebrand disease, platelet type

F2
(UniProt - OMIM)
 GP1BA
(UniProt - OMIM)
F5
(UniProt - OMIM)
PROZ
(UniProt - OMIM)

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


Citations in the biomedical literature:


Cerebral sinovenous thrombosis
F2 F5 PROZ
Von Willebrand disease, platelet type
GP1BA



Cerebral sinovenous thrombosis
Von Willebrand disease, platelet type

Synonym(s):
- CSVT
Synonym(s):
- PT-VWD
- Pseudo-Von Willebrand disease
- Pseudo-Von Willebrand disease type 2B
Classification (Orphanet):
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.