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FG syndrome type 1
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
FG syndrome type 1
Autosomal dominant secondary polycythemia

MED12
(UniProt - OMIM)
 EGLN1
(UniProt - OMIM)
EPAS1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
MED12
(0.63)
EPAS1


Citations in the biomedical literature:


FG syndrome type 1
MED12
Autosomal dominant secondary polycythemia
EGLN1 EPAS1



FG syndrome type 1
Autosomal dominant secondary polycythemia

Synonym(s):
- Opitz-Kaveggia syndrome
Synonym(s):
- Autosomal dominant secondary erythrocytosis
Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
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.