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

KIF21A MYC
PHOX2A
TUBB2B
TUBB3


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


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



Congenital fibrosis of extraocular muscles
Burkitt lymphoma

Synonym(s):
- FEOM

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

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

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

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

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

No signs/symptoms info available.