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Craniopharyngioma

2 associated genes
No signs/symptoms info

COMMON GENES: 1
PROTEIN INTERACTIONS: 1

Hepatocellular carcinoma, childhood-onset

2 associated genes
No signs/symptoms info

Craniopharyngioma

Hepatocellular carcinoma, childhood-onset

BRAF	(UniProt - OMIM)		CTNNB1	(UniProt - OMIM)
CTNNB1	(UniProt - OMIM)		MET	(UniProt - OMIM)


COMMON GENES	CTNNB1


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CTNNB1	(0.83)	MET

Citations in the biomedical literature:

Craniopharyngioma		Hepatocellular carcinoma, childhood-onset

	Classification (Orphanet): - Rare endocrine disease - Rare neurologic disease - Rare oncologic disease		Classification (Orphanet): - Rare hepatic disease - Rare oncologic disease

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

	Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: variable Average age of death: - Type of inheritance: sporadic		Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: sporadic

	External references: No OMIM references 1 MeSH reference: D003397		External references: No OMIM references No MeSH references

No signs/symptoms info available.