ODCs

Click node...

2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 2

1 OMIM reference -
2 associated genes
No signs/symptoms info

Hepatocellular carcinoma, childhood-onset

Familial capillary hemangioma

CTNNB1	(UniProt - OMIM)		ANTXR1	(UniProt - OMIM)
MET	(UniProt - OMIM)		KDR	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MET CTNNB1	(0.63) (0.52)	KDR KDR

Citations in the biomedical literature:

Hepatocellular carcinoma, childhood-onset		Familial capillary hemangioma

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

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Neoplasms -

	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: 1 OMIM reference - No MeSH references

No signs/symptoms info available.