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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 3
1 OMIM reference -
1 associated gene
No signs/symptoms info
Von Willebrand disease type 2M
Von Willebrand disease type 3

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

COMMON
GENES 		VWF


Citations in the biomedical literature:


Von Willebrand disease type 2M
VWF
Von Willebrand disease type 3



Von Willebrand disease type 2M
Von Willebrand disease type 3

Synonym(s):
(no synonyms)

Synonym(s):
- Willebrand disease type 3
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: 1-9 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D056729
No signs/symptoms info available.