ODCs

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2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

3 OMIM references -
2 associated genes
No signs/symptoms info

Hepatocellular carcinoma, childhood-onset

Rieger anomaly

CTNNB1	(UniProt - OMIM)		FOXC1	(UniProt - OMIM)
MET	(UniProt - OMIM)		PITX2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CTNNB1	(0.85)	PITX2

Citations in the biomedical literature:

Hepatocellular carcinoma, childhood-onset		Rieger anomaly

	Classification (Orphanet): - Rare hepatic disease - Rare oncologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	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: 3 OMIM references - No MeSH references

No signs/symptoms info available.