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Congenital factor XII deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant secondary polycythemia
2 OMIM references -
2 associated genes
No signs/symptoms info
Congenital factor XII deficiency
Autosomal dominant secondary polycythemia

F12
(UniProt - OMIM)
 EGLN1
(UniProt - OMIM)
EPAS1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
F12
(0.68)
EPAS1


Citations in the biomedical literature:


Congenital factor XII deficiency
F12
Autosomal dominant secondary polycythemia
EGLN1 EPAS1



Congenital factor XII deficiency
Autosomal dominant secondary polycythemia

Synonym(s):
- Congenital Hageman factor deficiency
Synonym(s):
- Autosomal dominant secondary erythrocytosis
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:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.