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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
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Burkitt lymphoma

LMNA MYC


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
LMNA
(0.82)
MYC



Citations in the biomedical literature:


Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
LMNA
Burkitt lymphoma
MYC



Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Burkitt lymphoma

Synonym(s):
(no synonyms)

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

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

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

Epidemiological data:
Class of prevalence: unknown
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:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
2 MeSH references: D002051 / D008228

No signs/symptoms info available.