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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Quebec platelet disorder
Congenital plasminogen activator inhibitor type 1 deficiency

PLAU SERPINE1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PLAU
(0.88)
SERPINE1



Citations in the biomedical literature:


Quebec platelet disorder
PLAU
Congenital plasminogen activator inhibitor type 1 deficiency
SERPINE1



Quebec platelet disorder
Congenital plasminogen activator inhibitor type 1 deficiency

Synonym(s):
- Factor V Quebec

Synonym(s):
- Congenital PAI-1 deficiency

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

Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
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: childhood
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: C536260
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.