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

F2 ACTN1
F5 ITGA2B
PROZ ITGB3
TUBB1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
F2
(0.75)
ITGA2B



Citations in the biomedical literature:


Cerebral sinovenous thrombosis
F2 F5 PROZ
Autosomal dominant macrothrombocytopenia
ACTN1 ITGA2B ITGB3 TUBB1



Cerebral sinovenous thrombosis
Autosomal dominant macrothrombocytopenia

Synonym(s):
- CSVT

Synonym(s):
(no synonyms)

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: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

External references:
No OMIM references
No MeSH references
External references:
3 OMIM references -
No MeSH references

No signs/symptoms info available.