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Autosomal codominant severe lipodystrophic laminopathy
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Atypical Werner syndrome
1 associated gene
No signs/symptoms info
Autosomal codominant severe lipodystrophic laminopathy
Atypical Werner syndrome

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

COMMON
GENES 		LMNA


Citations in the biomedical literature:


Autosomal codominant severe lipodystrophic laminopathy
LMNA
Atypical Werner syndrome



Autosomal codominant severe lipodystrophic laminopathy
Atypical Werner syndrome

Synonym(s):
(no synonyms)

Synonym(s):
- Atypical progeroid syndrome
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
- Rare skin disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.