ODCs

Click node...

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

PROTEIN INTERACTIONS: 2

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

Von Willebrand disease type 2M

Osteogenesis imperfecta type 1

VWF	(UniProt - OMIM)		COL1A1	(UniProt - OMIM)
			COL1A2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	VWF VWF	(0.76) (0.52)	COL1A1 COL1A2

Citations in the biomedical literature:

Von Willebrand disease type 2M		Osteogenesis imperfecta type 1
	Synonym(s): (no synonyms)		Synonym(s): - Adair-Dighton syndrome - Mild osteogenesis imperfecta - Non-deforming osteogenesis imperfecta - OI type 1 - Van der Hoeve syndrome

	Classification (Orphanet): - Rare genetic disease - Rare hematologic disease		Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

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

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

No signs/symptoms info available.