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Von Willebrand disease type 2M
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Von Willebrand disease type 2A
1 OMIM reference -
1 associated gene
No signs/symptoms info
Von Willebrand disease type 2M
Von Willebrand disease type 2A

VWF
(UniProt - OMIM)
 VWF
(UniProt - OMIM)

COMMON
GENES 		VWF


Citations in the biomedical literature:


Von Willebrand disease type 2M
VWF
Von Willebrand disease type 2A



Von Willebrand disease type 2M
Von Willebrand disease type 2A

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: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.