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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
6 OMIM references -
4 associated genes
No signs/symptoms info
Burkitt lymphoma
Congenital fibrosis of extraocular muscles

MYC KIF21A
PHOX2A
TUBB2B
TUBB3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
MYC
(0.63)
TUBB3



Citations in the biomedical literature:


Burkitt lymphoma
MYC
Congenital fibrosis of extraocular muscles
KIF21A PHOX2A TUBB2B TUBB3



Burkitt lymphoma
Congenital fibrosis of extraocular muscles

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

Synonym(s):
- FEOM

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

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Diseases of the eye and adnexa -

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: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.