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Oculootodental syndrome
1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Pediatric systemic lupus erythematosus
4 associated genes
No signs/symptoms info
Oculootodental syndrome
Pediatric systemic lupus erythematosus

FADD
(UniProt - OMIM)
 IRAK1
(UniProt - OMIM)
FGF3
(UniProt - OMIM)
 PTPN22
(UniProt - OMIM)
SPP1
(UniProt - OMIM)
STAT4
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
FADD
(0.52)
IRAK1


Citations in the biomedical literature:


Oculootodental syndrome
FADD FGF3
Pediatric systemic lupus erythematosus
IRAK1 PTPN22 SPP1 STAT4



Oculootodental syndrome
Pediatric systemic lupus erythematosus

Synonym(s):
- OOD
Synonym(s):
- SLE, pediatric onset
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare odontologic disease
Classification (Orphanet):
- Rare neurologic disease
- Rare renal disease
- Rare respiratory disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Diseases of the digestive 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.