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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 2A
Osteogenesis imperfecta type 1

VWF COL1A1
COL1A2


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 2A
VWF
Osteogenesis imperfecta type 1
COL1A1 COL1A2



Von Willebrand disease type 2A
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.