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Burkitt lymphoma

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

PROTEIN INTERACTIONS: 1

Griscelli disease type 1

1 OMIM reference -
1 associated gene
12 signs/symptoms

Burkitt lymphoma

Griscelli disease type 1

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MYC	(0.63)	MYO5A

Citations in the biomedical literature:

Burkitt lymphoma		Griscelli disease type 1
	Synonym(s): - Small non-cleaved cell lymphoma		Synonym(s): - Griscelli-PruniÃ©ras syndrome type 1 - Hypopigmentation - neurologic impairment

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

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: any age Type of inheritance: sporadic		Epidemiological data: (no data available)

	External references: 1 OMIM reference - 2 MeSH references: D002051 / D008228		External references: 1 OMIM reference - 1 MeSH reference: C537301

Griscelli disease type 1
	Very frequent - Albinism (hair) - Ataxia / incoordination / trouble of the equilibrium - Diffuse / generalised skin hypopigmentation / cutaneous albinism - Hypertonia / spasticity / rigidity / stiffness - Iris albinism / ocular albinism - Movement disorder - Nystagmus - Premature greying of hair - Seizures / epilepsy / absences / spasms / status epilepticus Frequent - Hyperlipidemia / hypercholesterolemia / hypertriglyceridemia - Intellectual deficit / mental / psychomotor retardation / learning disability Occasional - Intracranial / cerebral calcifications
Burkitt lymphoma
(no data available)