Cytoscape Web
Click node...

Cerebral sinovenous thrombosis
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant severe congenital neutropenia
4 OMIM references -
2 associated genes
No signs/symptoms info
Cerebral sinovenous thrombosis
Autosomal dominant severe congenital neutropenia

F2
(UniProt - OMIM)
 ELANE
(UniProt - OMIM)
F5
(UniProt - OMIM)
 GFI1
(UniProt - OMIM)
PROZ
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
F5
(0.52)
ELANE


Citations in the biomedical literature:


Cerebral sinovenous thrombosis
F2 F5 PROZ
Autosomal dominant severe congenital neutropenia
ELANE GFI1



Cerebral sinovenous thrombosis
Autosomal dominant severe congenital neutropenia

Synonym(s):
- CSVT
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare immune 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: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: any age
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
External references:
4 OMIM references -
No MeSH references
No signs/symptoms info available.