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

IRAK1 EGLN1
PTPN22 EPAS1
SPP1
STAT4


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


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



Pediatric systemic lupus erythematosus
Autosomal dominant secondary polycythemia

Synonym(s):
- SLE, pediatric onset

Synonym(s):
- Autosomal dominant secondary erythrocytosis

Classification (Orphanet):
- Rare neurologic disease
- Rare renal disease
- Rare respiratory disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease

Classification (ICD10):
- Diseases of the musculoskeletal system and connective tissue -
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:
No OMIM references
No MeSH references
External references:
2 OMIM references -
No MeSH references

No signs/symptoms info available.