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4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
4 associated genes
No signs/symptoms info
Pediatric systemic lupus erythematosus
Severe congenital nemaline myopathy

IRAK1 ACTA1
PTPN22 KLHL40
SPP1 KLHL41
STAT4 NEB


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PTPN22
(0.63)
ACTA1



Citations in the biomedical literature:


Pediatric systemic lupus erythematosus
IRAK1 PTPN22 SPP1 STAT4
Severe congenital nemaline myopathy
ACTA1 KLHL40 KLHL41 NEB



Pediatric systemic lupus erythematosus
Severe congenital nemaline myopathy

Synonym(s):
- SLE, pediatric onset

Synonym(s):
(no synonyms)

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

Classification (ICD10):
- Diseases of the musculoskeletal system and connective tissue -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: child / adolescent
Type of inheritance: autosomal recessive

External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.