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Congenital factor XII deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
1 OMIM reference -
1 associated gene
No signs/symptoms info
Congenital factor XII deficiency
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

F12
(UniProt - OMIM)
 APP
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
F12
(0.62)
APP


Citations in the biomedical literature:


Congenital factor XII deficiency
F12
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Congenital factor XII deficiency
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
- Congenital Hageman factor deficiency
Synonym(s):
- HCHWA, Flemish type
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
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.