ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 2

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

Symptomatic form of hemophilia A in female carriers

Combined deficiency of factor V and factor VIII

F8	(UniProt - OMIM)		LMAN1	(UniProt - OMIM)
			MCFD2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	F8 F8	(0.73) (0.52)	LMAN1 MCFD2

Citations in the biomedical literature:

Symptomatic form of hemophilia A in female carriers		Combined deficiency of factor V and factor VIII
	Synonym(s): (no synonyms)		Synonym(s): - F5F8D - FV and FVIII combined deficiency - Familial multiple coagulation factor deficiency

	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: unknown Average age onset: - Average age of death: - Type of inheritance: x-linked recessive		Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: variable Average age of death: any age Type of inheritance: autosomal recessive

	External references: No OMIM references No MeSH references		External references: 3 OMIM references - No MeSH references

No signs/symptoms info available.