ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Sporadic pheochromocytoma

Familial multiple meningioma


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	EPAS1	(0.63)	SMARCB1

Citations in the biomedical literature:

Sporadic pheochromocytoma		Familial multiple meningioma

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

	Classification (ICD10): (no data available)		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: unknown Average age onset: - Average age of death: - Type of inheritance: sporadic		Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.