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4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
3 OMIM references -
5 associated genes
No signs/symptoms info
Pediatric systemic lupus erythematosus
Autoimmune lymphoproliferative syndrome

IRAK1 CASP10
PTPN22 FAS
SPP1 FASLG
STAT4 NRAS
PRKCD


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PTPN22
IRAK1
(0.68)
(0.63)
PRKCD
PRKCD



Citations in the biomedical literature:


Pediatric systemic lupus erythematosus
IRAK1 PTPN22 SPP1 STAT4
Autoimmune lymphoproliferative syndrome
CASP10 FAS FASLG NRAS PRKCD



Pediatric systemic lupus erythematosus
Autoimmune lymphoproliferative syndrome

Synonym(s):
- SLE, pediatric onset

Synonym(s):
- ALPS
- Canale-Smith syndrome
- FAS deficiency

Classification (Orphanet):
- Rare neurologic disease
- Rare renal disease
- Rare respiratory disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
- Rare immune disease
- Rare oncologic 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: variable
Average age of death: -
Type of inheritance: autosomal dominant

External references:
No OMIM references
No MeSH references
External references:
3 OMIM references -
1 MeSH reference: D056735

No signs/symptoms info available.