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Burkitt lymphoma

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

PROTEIN INTERACTIONS: 1

Autosomal recessive ataxia, Beauce type

1 OMIM reference -
1 associated gene
1 sign/symptom

Burkitt lymphoma

Autosomal recessive ataxia, Beauce type

(UniProt - OMIM)

(UniProt - OMIM)


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

Citations in the biomedical literature:

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

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

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

	Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: any age Type of inheritance: sporadic		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

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

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