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Progeria-associated arthropathy
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Autosomal codominant severe lipodystrophic laminopathy
1 associated gene
No signs/symptoms info
Progeria-associated arthropathy
Autosomal codominant severe lipodystrophic laminopathy

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

COMMON
GENES 		LMNA


Citations in the biomedical literature:


Progeria-associated arthropathy
LMNA
Autosomal codominant severe lipodystrophic laminopathy



Progeria-associated arthropathy
Autosomal codominant severe lipodystrophic laminopathy

Classification (Orphanet):
- Rare genetic disease
- Rare systemic or rheumatologic 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:
(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
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.