ODCs

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

COMMON GENES: 1
PROTEIN INTERACTIONS: 2

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

Bernard-Soulier syndrome

Von Willebrand disease, platelet type


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	GP9 GP1BB	(0.65) (0.62)	GP1BA GP1BA

Citations in the biomedical literature:

Bernard-Soulier syndrome		Von Willebrand disease, platelet type
	Synonym(s): - Giant platelet syndrome - Hemorrhagiparous thrombocytic dystrophy		Synonym(s): - PT-VWD - Pseudo-Von Willebrand disease - Pseudo-Von Willebrand disease type 2B

	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: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

	External references: 2 OMIM references - 1 MeSH reference: D001606		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.