ODCs

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

PROTEIN INTERACTIONS: 1

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

Spinocerebellar ataxia with epilepsy

Burkitt lymphoma


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	POLG	(0.63)	MYC

Citations in the biomedical literature:

Spinocerebellar ataxia with epilepsy		Burkitt lymphoma
	Synonym(s): - MSCAE - Mitochondrial spinocerebellar ataxia with epilepsy - SCAE		Synonym(s): - Small non-cleaved cell lymphoma

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

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

	Epidemiological data: Class of prevalence: - Average age onset: adolescence / young Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: any age Type of inheritance: sporadic

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 2 MeSH references: D002051 / D008228

No signs/symptoms info available.