Cytoscape Web
Click node...


1 associated gene
No signs/symptoms info
COMMON GENES: 1
1 associated gene
No signs/symptoms info
Laminopathy type Decaudain-Vigouroux
Autosomal codominant severe lipodystrophic laminopathy

LMNA LMNA


COMMON
GENES
LMNA



Citations in the biomedical literature:


Laminopathy type Decaudain-Vigouroux
LMNA
Autosomal codominant severe lipodystrophic laminopathy



Laminopathy type Decaudain-Vigouroux
Autosomal codominant severe lipodystrophic laminopathy

Synonym(s):
- Laminopathy with severe metabolic syndrome and myopathy

Synonym(s):
(no synonyms)

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

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
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.