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1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
1 associated gene
No signs/symptoms info
Autosomal dominant limb-girdle muscular dystrophy type 1B
Autosomal codominant severe lipodystrophic laminopathy

LMNA LMNA


COMMON
GENES
LMNA



Citations in the biomedical literature:


Autosomal dominant limb-girdle muscular dystrophy type 1B
LMNA
Autosomal codominant severe lipodystrophic laminopathy



Autosomal dominant limb-girdle muscular dystrophy type 1B
Autosomal codominant severe lipodystrophic laminopathy

Synonym(s):
- LGMD1B
- Limb-girdle muscular dystrophy due to lamin A/C deficiency

Synonym(s):
(no synonyms)

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

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

Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: childhood
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.