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

LMNA
(UniProt - OMIM)
 ALK
(UniProt - OMIM)
CARS
(UniProt - OMIM)
CLTC
(UniProt - OMIM)
RANBP2
(UniProt - OMIM)
TPM3
(UniProt - OMIM)
TPM4
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
LMNA
(0.49)
RANBP2


Citations in the biomedical literature:


Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
LMNA
Inflammatory myofibroblastic tumor
ALK CARS CLTC RANBP2 TPM3 TPM4



Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Inflammatory myofibroblastic tumor

Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (Orphanet):
- Rare oncologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.