ODCs

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2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Craniopharyngioma

Autosomal dominant Emery-Dreifuss muscular dystrophy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CTNNB1	(0.63)	LMNA

Citations in the biomedical literature:

Craniopharyngioma		Autosomal dominant Emery-Dreifuss muscular dystrophy

	Classification (Orphanet): - Rare endocrine disease - Rare neurologic disease - Rare oncologic disease		Classification (Orphanet): - Rare cardiac disease - 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: (no data available)

	External references: No OMIM references 1 MeSH reference: D003397		External references: 4 OMIM references - No MeSH references

No signs/symptoms info available.