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Congenital high-molecular-weight kininogen deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Von Willebrand disease, platelet type
1 OMIM reference -
1 associated gene
No signs/symptoms info
Congenital high-molecular-weight kininogen deficiency
Von Willebrand disease, platelet type

KNG1
(UniProt - OMIM)
 GP1BA
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
KNG1
(0.55)
GP1BA


Citations in the biomedical literature:


Congenital high-molecular-weight kininogen deficiency
KNG1
Von Willebrand disease, platelet type
GP1BA



Congenital high-molecular-weight kininogen deficiency
Von Willebrand disease, platelet type

Synonym(s):
(no synonyms)

Synonym(s):
- PT-VWD
- Pseudo-Von Willebrand disease
- Pseudo-Von Willebrand disease type 2B
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 recessive
Epidemiological data:
Class of prevalence: -
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.