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Myxofibrosarcoma
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
1 OMIM reference -
1 associated gene
No signs/symptoms info
Myxofibrosarcoma
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation

CREB3L1
(UniProt)
 LMNA
(UniProt - OMIM)
CREB3L2
(UniProt - OMIM)
FUS
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
FUS
(0.49)
LMNA


Citations in the biomedical literature:


Myxofibrosarcoma
CREB3L1 CREB3L2 FUS
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
LMNA



Myxofibrosarcoma
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation

Synonym(s):
- Fibromyxosarcoma
- Myxoid malignant fibrous histiocytoma
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare neurologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.