ODCs

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2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 3

16 OMIM references -
4 associated genes
No signs/symptoms info

Craniopharyngioma

Early-onset autosomal dominant Alzheimer disease


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CTNNB1 CTNNB1 CTNNB1	(0.97) (0.56) (0.52)	PSEN1 APP PSEN2

Citations in the biomedical literature:

Craniopharyngioma		Early-onset autosomal dominant Alzheimer disease
	Synonym(s): (no synonyms)		Synonym(s): - EOFAD - Early-onset familial autosomal dominant Alzheimer disease - Familial Alzheimer disease

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

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Diseases of the nervous system -

	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: 1-9 / 100 000 Average age onset: adulthood Average age of death: adult Type of inheritance: autosomal dominant

	External references: No OMIM references 1 MeSH reference: D003397		External references: 16 OMIM references - No MeSH references

No signs/symptoms info available.