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4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
2 associated genes
No signs/symptoms info
Pediatric systemic lupus erythematosus
Familial medullary thyroid carcinoma

IRAK1 NTRK1
PTPN22 RET
SPP1
STAT4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PTPN22
(0.68)
NTRK1



Citations in the biomedical literature:


Pediatric systemic lupus erythematosus
IRAK1 PTPN22 SPP1 STAT4
Familial medullary thyroid carcinoma
NTRK1 RET



Pediatric systemic lupus erythematosus
Familial medullary thyroid carcinoma

Synonym(s):
- SLE, pediatric onset

Synonym(s):
- Familial MTC

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

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

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: C536911

No signs/symptoms info available.