ODCs

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2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 2

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

High bone mass osteogenesis imperfecta

Von Willebrand disease type 1

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


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

Citations in the biomedical literature:

High bone mass osteogenesis imperfecta		Von Willebrand disease type 1
	Synonym(s): - High bone mass OI		Synonym(s): - Willebrand disease type 1

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		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: childhood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-5 / 10 000 Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.