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3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
2 associated genes
No signs/symptoms info
Cerebral sinovenous thrombosis
Glanzmann thrombasthenia

F2 ITGA2B
F5 ITGB3
PROZ


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
Glanzmann thrombasthenia
ITGA2B ITGB3



Cerebral sinovenous thrombosis
Glanzmann thrombasthenia

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: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive

External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.