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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
Hypohidrotic ectodermal dysplasia with immunodeficiency

IRAK1 IKBKG
PTPN22 NFKBIA
SPP1
STAT4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
IRAK1
(0.9)
IKBKG



Citations in the biomedical literature:


Pediatric systemic lupus erythematosus
IRAK1 PTPN22 SPP1 STAT4
Hypohidrotic ectodermal dysplasia with immunodeficiency
IKBKG NFKBIA



Pediatric systemic lupus erythematosus
Hypohidrotic ectodermal dysplasia with immunodeficiency

Synonym(s):
- SLE, pediatric onset

Synonym(s):
- Anhidrotic ectodermal dysplasia with immunodeficiency
- EDA-ID
- HED-ID

Classification (Orphanet):
- Rare neurologic disease
- Rare renal disease
- Rare respiratory disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare immune disease
- Rare skin 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: neonatal/infancy
Average age of death: child / adolescent
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.