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Autosomal codominant severe lipodystrophic laminopathy
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
1 OMIM reference -
1 associated gene
No signs/symptoms info
Autosomal codominant severe lipodystrophic laminopathy
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation

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

COMMON
GENES 		LMNA


Citations in the biomedical literature:


Autosomal codominant severe lipodystrophic laminopathy
LMNA
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation



Autosomal codominant severe lipodystrophic laminopathy
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation

Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
- Rare skin disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
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.