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Alpers syndrome

1 OMIM reference -
1 associated gene
10 signs/symptoms

PROTEIN INTERACTIONS: 1

Burkitt lymphoma

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

Alpers syndrome

Burkitt lymphoma

(UniProt - OMIM)

(UniProt - OMIM)


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

Citations in the biomedical literature:

Alpers syndrome		Burkitt lymphoma
	Synonym(s): - Alpers progressive sclerosing poliodystrophy - Alpers-Huttenlocher syndrome - Progressive neuronal degeneration of childhood with liver disease		Synonym(s): - Small non-cleaved cell lymphoma

	Classification (Orphanet): - Inborn errors of metabolism - 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: neonatal/infancy 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 - 1 MeSH reference: D002549		External references: 1 OMIM reference - 2 MeSH references: D002051 / D008228

Alpers syndrome
	Frequent - Anomalies of eyes and vision - Ataxia / incoordination / trouble of the equilibrium - Autosomal recessive inheritance - Hemiplegia / diplegia / hemiparesia / limb palsy - Hypertonia / spasticity / rigidity / stiffness - Hypotonia - Intellectual deficit / mental / psychomotor retardation / learning disability - Microcephaly - Movement disorder - Seizures / epilepsy / absences / spasms / status epilepticus
Burkitt lymphoma
(no data available)