ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
4 associated genes
No signs/symptoms info

Congenital factor V deficiency

Myelofibrosis with myeloid metaplasia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	F5	(0.73)	CALR

Citations in the biomedical literature:

Congenital factor V deficiency		Myelofibrosis with myeloid metaplasia
	Synonym(s): - Owren disease - Parahemophilia - Proaccelerin deficiency		Synonym(s): - Agnogenic myeloid metaplasia - Idiopathic myelofibrosis - Myelosclerosis with myeloid metaplasia - Primary myelofibrosis

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

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): - Neoplasms -

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

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

No signs/symptoms info available.