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Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Laminopathy type Decaudain-Vigouroux
1 associated gene
No signs/symptoms info
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Laminopathy type Decaudain-Vigouroux

LMNA
(UniProt - OMIM)
 LMNA
(UniProt - OMIM)

COMMON
GENES 		LMNA


Citations in the biomedical literature:


Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
LMNA
Laminopathy type Decaudain-Vigouroux



Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Laminopathy type Decaudain-Vigouroux

Synonym(s):
(no synonyms)

Synonym(s):
- Laminopathy with severe metabolic syndrome and myopathy
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
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.