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Congenital myopathy with excess of thin filaments
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Pediatric systemic lupus erythematosus
4 associated genes
No signs/symptoms info
Congenital myopathy with excess of thin filaments
Pediatric systemic lupus erythematosus

ACTA1
(UniProt - OMIM)
 IRAK1
(UniProt - OMIM)
PTPN22
(UniProt - OMIM)
SPP1
(UniProt - OMIM)
STAT4
(UniProt - OMIM)

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


Citations in the biomedical literature:


Congenital myopathy with excess of thin filaments
ACTA1
Pediatric systemic lupus erythematosus
IRAK1 PTPN22 SPP1 STAT4



Congenital myopathy with excess of thin filaments
Pediatric systemic lupus erythematosus

Synonym(s):
- Actin myopathy
Synonym(s):
- SLE, pediatric onset
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare neurologic disease
- Rare renal disease
- Rare respiratory disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the musculoskeletal system and connective tissue -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.