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Autosomal recessive ataxia, Beauce type

1 OMIM reference -
1 associated gene
1 sign/symptom

PROTEIN INTERACTIONS: 1

Burkitt lymphoma

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

Autosomal recessive ataxia, Beauce type

Burkitt lymphoma

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SYNE1	(0.63)	MYC

Citations in the biomedical literature:

Autosomal recessive ataxia, Beauce type		Burkitt lymphoma
	Synonym(s): - ARCA1 - Autosomal recessive cerebellar ataxia type 1 - SCAR8		Synonym(s): - Small non-cleaved cell lymphoma

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

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

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: no data available 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

Autosomal recessive ataxia, Beauce type
	Very frequent - Ataxia / incoordination / trouble of the equilibrium
Burkitt lymphoma
(no data available)