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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
X-linked Emery-Dreifuss muscular dystrophy

IRAK1 EMD
PTPN22 FHL1
SPP1
STAT4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
STAT4
(0.63)
FHL1



Citations in the biomedical literature:


Pediatric systemic lupus erythematosus
IRAK1 PTPN22 SPP1 STAT4
X-linked Emery-Dreifuss muscular dystrophy
EMD FHL1



Pediatric systemic lupus erythematosus
X-linked Emery-Dreifuss muscular dystrophy

Synonym(s):
- SLE, pediatric onset

Synonym(s):
- EDMD1

Classification (Orphanet):
- Rare neurologic disease
- Rare renal disease
- Rare respiratory disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare cardiac disease
- 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: unknown
Average age onset: -
Average age of death: -
Type of inheritance: x-linked recessive

External references:
No OMIM references
No MeSH references
External references:
2 OMIM references -
No MeSH references

No signs/symptoms info available.