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2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Hepatocellular carcinoma, childhood-onset
Hereditary hypotrichosis with recurrent skin vesicles

CTNNB1 DSC3
MET


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CTNNB1
(0.73)
DSC3



Citations in the biomedical literature:


Hepatocellular carcinoma, childhood-onset
CTNNB1 MET
Hereditary hypotrichosis with recurrent skin vesicles
DSC3



Hepatocellular carcinoma, childhood-onset
Hereditary hypotrichosis with recurrent skin vesicles

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

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
(no data available)

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: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive

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

No signs/symptoms info available.