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Congenital factor XIII deficiency

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

PROTEIN INTERACTIONS: 3

Familial afibrinogenemia

1 OMIM reference -
3 associated genes
8 signs/symptoms

Congenital factor XIII deficiency

Familial afibrinogenemia

F13A1	(UniProt - OMIM)		FGA	(UniProt - OMIM)
F13B	(UniProt - OMIM)		FGB	(UniProt - OMIM)
			FGG	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	F13A1 F13A1 F13B	(0.78) (0.63) (0.58)	FGA FGG FGG

Citations in the biomedical literature:

Congenital factor XIII deficiency		Familial afibrinogenemia
	Synonym(s): - Fibrin-stabilizing factor deficiency		Synonym(s): (no synonyms)

	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: Class of prevalence: <1 / 1 000 000 Average age onset: variable Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

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

Familial afibrinogenemia
	Very frequent - Autosomal recessive inheritance - Epistaxis / nose bleeding - Gingivorrhagia / gingival bleeding - Hemorrhage / hemorrhagic syndrome / excessive / long-lasting bleeding - Hydrarthrosis / articular / joint effusion - Metrorrhagia / menorrhagia / hemorrhagic cycles / hyper / poly / spanio / dysmenorrhea - Spontaneous abortions Occasional - Intracranial / cerebral / meningeal hemorrhage
Congenital factor XIII deficiency
(no data available)