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4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
4 OMIM references -
5 associated genes
No signs/symptoms info
Pediatric systemic lupus erythematosus
Hereditary spherocytosis

IRAK1 ANK1
PTPN22 EPB42
SPP1 SLC4A1
STAT4 SPTA1
SPTB


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PTPN22
(0.63)
SPTA1



Citations in the biomedical literature:


Pediatric systemic lupus erythematosus
IRAK1 PTPN22 SPP1 STAT4
Hereditary spherocytosis
ANK1 EPB42 SLC4A1 SPTA1 SPTB



Pediatric systemic lupus erythematosus
Hereditary spherocytosis

Synonym(s):
- SLE, pediatric onset

Synonym(s):
- Minkowski-Chauffard disease

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: 1-5 / 10 000
Average age onset: variable
Average age of death: normal
Type of inheritance: autosomal dominant

External references:
No OMIM references
No MeSH references
External references:
4 OMIM references -
2 MeSH references: C536356 / D013103

No signs/symptoms info available.