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Burkitt lymphoma
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal recessive myogenic arthrogryposis multiplex congenita
1 associated gene
No signs/symptoms info
Burkitt lymphoma
Autosomal recessive myogenic arthrogryposis multiplex congenita

MYC
(UniProt - OMIM)
 SYNE1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
MYC
(0.63)
SYNE1


Citations in the biomedical literature:


Burkitt lymphoma
MYC
Autosomal recessive myogenic arthrogryposis multiplex congenita
SYNE1



Burkitt lymphoma
Autosomal recessive myogenic arthrogryposis multiplex congenita

Synonym(s):
- Small non-cleaved cell lymphoma
Synonym(s):
- Autosomal recessive myogenic AMC
- SYNE1-related AMC
- SYNE1-related arthrogryposis multiplex congenita
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
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:
No OMIM references
No MeSH references
No signs/symptoms info available.