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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
3 associated genes
No signs/symptoms info
Congenital factor XI deficiency
Cerebral sinovenous thrombosis

F11 F2
F5
PROZ


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
F11
(0.52)
F2



Citations in the biomedical literature:


Congenital factor XI deficiency
F11
Cerebral sinovenous thrombosis
F2 F5 PROZ



Congenital factor XI deficiency
Cerebral sinovenous thrombosis

Synonym(s):
- Hemophilia C
- PTA deficiency
- Plasma thromboplastin antecedent deficiency
- Rosenthal factor deficiency
- Rosenthal syndrome

Synonym(s):
- CSVT

Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare neurologic disease

Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: variable
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

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

No signs/symptoms info available.