ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Familial multiple meningioma

Cardiomyopathy - hypotonia - lactic acidosis


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SMARCE1	(0.63)	SLC25A3

Citations in the biomedical literature:

Familial multiple meningioma		Cardiomyopathy - hypotonia - lactic acidosis

	Classification (Orphanet): - Rare neurologic disease - Rare oncologic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare cardiac disease - Rare genetic disease

	Classification (ICD10): (no data available)		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

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

No signs/symptoms info available.