ODCs

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2 OMIM references -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
3 associated genes
6 signs/symptoms

Hereditary combined deficiency of vitamin K-dependent clotting factors

Familial dysfibrinogenemia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	VKORC1	(0.63)	FGG

Citations in the biomedical literature:

Hereditary combined deficiency of vitamin K-dependent clotting factors		Familial dysfibrinogenemia
	Synonym(s): - Hereditary combined deficiency of factors II, VII, IX and X		Synonym(s): (no synonyms)

	Classification (Orphanet): - Inborn errors of metabolism - 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: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant

	External references: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

Familial dysfibrinogenemia
	Very frequent - Autosomal dominant inheritance - Epistaxis / nose bleeding - Gastrointestinal bleeding / hemorrhage / hematemesis / melena / rectorrhagia - Gingivorrhagia / gingival bleeding - Hemorrhage / hemorrhagic syndrome / excessive / long-lasting bleeding Frequent - Venous thrombosis / phlebitis / thrombophlebitis
Hereditary combined deficiency of vitamin K-dependent clotting factors
(no data available)