ODCs

Click node...

1 OMIM reference -
1 associated gene
No signs/symptoms info

COMMON GENES: 1

1 associated gene
No signs/symptoms info

Familial dilated cardiomyopathy with conduction defect due to LMNA mutation

Autosomal codominant severe lipodystrophic laminopathy

LMNA

Citations in the biomedical literature:

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

	Classification (Orphanet): - Rare cardiac disease - Rare genetic disease		Classification (Orphanet): - Rare endocrine disease - Rare genetic disease - Rare skin 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: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.