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Autosomal dominant secondary polycythemia
2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Pediatric systemic lupus erythematosus
4 associated genes
No signs/symptoms info
Autosomal dominant secondary polycythemia
Pediatric systemic lupus erythematosus

EGLN1
(UniProt - OMIM)
 IRAK1
(UniProt - OMIM)
EPAS1
(UniProt - OMIM)
 PTPN22
(UniProt - OMIM)
SPP1
(UniProt - OMIM)
STAT4
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
EPAS1
(0.63)
SPP1


Citations in the biomedical literature:


Autosomal dominant secondary polycythemia
EGLN1 EPAS1
Pediatric systemic lupus erythematosus
IRAK1 PTPN22 SPP1 STAT4



Autosomal dominant secondary polycythemia
Pediatric systemic lupus erythematosus

Synonym(s):
- Autosomal dominant secondary erythrocytosis
Synonym(s):
- SLE, pediatric onset
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare neurologic disease
- Rare renal disease
- Rare respiratory 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):
- Diseases of the musculoskeletal system and connective tissue -
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
2 OMIM references -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.