ODCs

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1 associated gene
No signs/symptoms info

COMMON GENES: 1

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

Autosomal codominant severe lipodystrophic laminopathy

Autosomal dominant limb-girdle muscular dystrophy type 1B

LMNA

Citations in the biomedical literature:

Autosomal codominant severe lipodystrophic laminopathy		Autosomal dominant limb-girdle muscular dystrophy type 1B
	Synonym(s): (no synonyms)		Synonym(s): - LGMD1B - Limb-girdle muscular dystrophy due to lamin A/C deficiency

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

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Diseases of the nervous system -

	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: 1-9 / 1 000 000 Average age onset: childhood 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.