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

F8
(UniProt - OMIM)
 VWF
(UniProt - OMIM)

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


Citations in the biomedical literature:


Mild hemophilia A
F8
Von Willebrand disease type 2N
VWF



Mild hemophilia A
Von Willebrand disease type 2N

Synonym(s):
- Mild factor VIII deficiency
Synonym(s):
(no synonyms)
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: 1-9 / 100 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: x-linked recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.