ODCs

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2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Hepatocellular carcinoma, childhood-onset

Autosomal codominant severe lipodystrophic laminopathy

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		Autosomal codominant severe lipodystrophic laminopathy

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