ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
3 associated genes
5 signs/symptoms

Congenital alpha2 antiplasmin deficiency

Familial hypofibrinogenemia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SERPINF2	(0.62)	FGA

Citations in the biomedical literature:

Congenital alpha2 antiplasmin deficiency		Familial hypofibrinogenemia

	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: 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 hypofibrinogenemia
	Very frequent - Autosomal dominant inheritance - Epistaxis / nose bleeding - Gastrointestinal bleeding / hemorrhage / hematemesis / melena / rectorrhagia - Gingivorrhagia / gingival bleeding - Hemorrhage / hemorrhagic syndrome / excessive / long-lasting bleeding
Congenital alpha2 antiplasmin deficiency
(no data available)