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Progeria-associated arthropathy
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Autosomal dominant limb-girdle muscular dystrophy type 1B
1 OMIM reference -
1 associated gene
No signs/symptoms info
Progeria-associated arthropathy
Autosomal dominant limb-girdle muscular dystrophy type 1B

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

COMMON
GENES 		LMNA


Citations in the biomedical literature:


Progeria-associated arthropathy
LMNA
Autosomal dominant limb-girdle muscular dystrophy type 1B



Progeria-associated arthropathy
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 genetic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
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.