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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
12 signs/symptoms
Burkitt lymphoma
X-linked sideroblastic anemia - ataxia

MYC ABCB7


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
MYC
(0.63)
ABCB7



Citations in the biomedical literature:


Burkitt lymphoma
MYC
X-linked sideroblastic anemia - ataxia
ABCB7



Burkitt lymphoma
X-linked sideroblastic anemia - ataxia

Synonym(s):
- Small non-cleaved cell lymphoma

Synonym(s):
(no synonyms)

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

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

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: neonatal/infancy
Average age of death: -
Type of inheritance: x-linked recessive

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

X-linked sideroblastic anemia - ataxia

Very frequent
- Anaemia
- Ataxia / incoordination / trouble of the equilibrium
- Nystagmus
- Speech troubles / aphasia / dysphasia / echolalia / mutism / logorrhea / dysprosodia
- X-linked recessive inheritance

Frequent
- Hypereflexia
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Movement disorder

Occasional
- Hypotonia
- Intrauterine growth retardation
- Scoliosis
- Strabismus / squint


Burkitt lymphoma

(no data available)