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Hepatocellular carcinoma, childhood-onset
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Atypical Werner syndrome
1 associated gene
No signs/symptoms info
Hepatocellular carcinoma, childhood-onset
Atypical Werner syndrome

CTNNB1
(UniProt - OMIM)
 LMNA
(UniProt - OMIM)
MET
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CTNNB1
(0.63)
LMNA


Citations in the biomedical literature:


Hepatocellular carcinoma, childhood-onset
CTNNB1 MET
Atypical Werner syndrome
LMNA



Hepatocellular carcinoma, childhood-onset
Atypical Werner syndrome

Synonym(s):
(no synonyms)

Synonym(s):
- Atypical progeroid syndrome
Classification (Orphanet):
- Rare hepatic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- 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:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.