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Von Willebrand disease, platelet type
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Congenital factor XII deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
Von Willebrand disease, platelet type
Congenital factor XII deficiency

GP1BA
(UniProt - OMIM)
 F12
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
GP1BA
(0.85)
F12


Citations in the biomedical literature:


Von Willebrand disease, platelet type
GP1BA
Congenital factor XII deficiency
F12



Von Willebrand disease, platelet type
Congenital factor XII deficiency

Synonym(s):
- PT-VWD
- Pseudo-Von Willebrand disease
- Pseudo-Von Willebrand disease type 2B
Synonym(s):
- Congenital Hageman factor deficiency
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: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.