ODCs

Click node...

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 factor II deficiency


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PLAU	(0.62)	F2

Citations in the biomedical literature:

Quebec platelet disorder		Congenital factor II deficiency
	Synonym(s): - Factor V Quebec		Synonym(s): - Dysprothrombinemia - Hypoprothrombinemia - Prothrombin 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: <1 / 1 000 000 Average age onset: variable Average age of death: any age Type of inheritance: autosomal recessive

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

No signs/symptoms info available.