ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
3 associated genes
6 signs/symptoms

Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency

Familial dysfibrinogenemia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HRG	(0.75)	FGA

Citations in the biomedical literature:

Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency		Familial dysfibrinogenemia
	Synonym(s): - Hereditary thrombophilia due to congenital HRG deficiency		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare bone disease - 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: variable Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 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 thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
(no data available)