Cytoscape Web
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1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 1
4 OMIM references -
4 associated genes
No signs/symptoms info
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Autosomal dominant Emery-Dreifuss muscular dystrophy

LMNA LMNA
SYNE1
SYNE2
TMEM43


COMMON
GENES
LMNA


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
LMNA
(0.88)
SYNE1



Citations in the biomedical literature:


Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
LMNA
Autosomal dominant Emery-Dreifuss muscular dystrophy
SYNE1 SYNE2 TMEM43



Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Autosomal dominant Emery-Dreifuss muscular dystrophy

Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the nervous system -

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:
4 OMIM references -
No MeSH references

No signs/symptoms info available.