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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
Von Willebrand disease type 2A
Severe hemophilia A

VWF F8


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
VWF
(0.88)
F8



Citations in the biomedical literature:


Von Willebrand disease type 2A
VWF
Severe hemophilia A
F8



Von Willebrand disease type 2A
Severe hemophilia A

Synonym(s):
(no synonyms)

Synonym(s):
- Severe factor VIII 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: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: x-linked recessive

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

No signs/symptoms info available.