ODCs

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

PROTEIN INTERACTIONS: 3

6 associated genes
No signs/symptoms info

Von Willebrand disease type 2M

Fetal and neonatal alloimmune thrombocytopenia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	VWF VWF VWF	(0.89) (0.55) (0.52)	GP1BA ITGA2B ITGB3

Citations in the biomedical literature:

Von Willebrand disease type 2M		Fetal and neonatal alloimmune thrombocytopenia
	Synonym(s): (no synonyms)		Synonym(s): - NAIT

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

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): - Certain conditions originating in the perinatal period -

	Epidemiological data: Class of prevalence: unknown Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

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

No signs/symptoms info available.