ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

2 associated genes
No signs/symptoms info

Familial adenomatous polyposis due to 5q22.2 microdeletion

Craniopharyngioma

APC	(UniProt - OMIM)		BRAF	(UniProt - OMIM)
			CTNNB1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	APC	(0.99)	CTNNB1

Citations in the biomedical literature:

Familial adenomatous polyposis due to 5q22.2 microdeletion		Craniopharyngioma
	Synonym(s): - Colorectal adenomatous polyposis due to monosomy 5q22.2 - FAP due to monosomy 5q22.2 - Familial adenomatous polyposis due to del(5)(q22.2) - Familial adenomatous polyposis due to monosomy 5q22.2 - Familial polyposis coli due to monosomy 5q22.2		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare gastroenterologic disease - Rare genetic disease - Rare oncologic disease		Classification (Orphanet): - Rare endocrine disease - Rare neurologic disease - Rare oncologic disease

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

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: variable Average age of death: - Type of inheritance: sporadic

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

No signs/symptoms info available.