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Inflammatory myofibroblastic tumor
6 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
Inflammatory myofibroblastic tumor
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation

ALK
(UniProt - OMIM)
 LMNA
(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)
RANBP2
(0.49)
LMNA


Citations in the biomedical literature:


Inflammatory myofibroblastic tumor
ALK CARS CLTC RANBP2 TPM3 TPM4

Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
LMNA



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

Classification (Orphanet):
- Rare oncologic disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
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.