ODCs

Cytoscape Web

Click node...

Congenital analbuminemia

1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Familial hypofibrinogenemia

1 OMIM reference -
3 associated genes
5 signs/symptoms

Congenital analbuminemia

Familial hypofibrinogenemia

ALB	(UniProt - OMIM)		FGA	(UniProt - OMIM)
			FGB	(UniProt - OMIM)
			FGG	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ALB	(0.72)	FGA

Citations in the biomedical literature:

Congenital analbuminemia		Familial hypofibrinogenemia

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

	Classification (ICD10): - Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified -		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: normal 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: No OMIM references 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 analbuminemia
(no data available)