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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Burkitt lymphoma
Intellectual disability-severe speech delay-mild dysmorphism syndrome

MYC FOXP1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
MYC
(0.72)
FOXP1



Citations in the biomedical literature:


Burkitt lymphoma
MYC
Intellectual disability-severe speech delay-mild dysmorphism syndrome
FOXP1



Burkitt lymphoma
Intellectual disability-severe speech delay-mild dysmorphism syndrome

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

Synonym(s):
(no synonyms)

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

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
(no data available)

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 -
No MeSH references

No signs/symptoms info available.