ODCs

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

PROTEIN INTERACTIONS: 2

1 OMIM reference -
2 associated genes
No signs/symptoms info

Von Willebrand disease type 1

Glanzmann thrombasthenia

VWF	(UniProt - OMIM)		ITGA2B	(UniProt - OMIM)
			ITGB3	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	VWF VWF	(0.55) (0.52)	ITGA2B ITGB3

Citations in the biomedical literature:

Von Willebrand disease type 1		Glanzmann thrombasthenia
	Synonym(s): - Willebrand disease type 1		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: 1-5 / 10 000 Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - 1 MeSH reference: D056725		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.