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2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hepatocellular carcinoma, childhood-onset
Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency

CTNNB1 SH2B1
MET


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
MET
(0.72)
SH2B1



Citations in the biomedical literature:


Hepatocellular carcinoma, childhood-onset
CTNNB1 MET
Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency
SH2B1



Hepatocellular carcinoma, childhood-onset
Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency

Classification (Orphanet):
- Rare hepatic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant

External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.