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1 associated gene
No signs/symptoms info
COMMON GENES: 1
1 associated gene
No signs/symptoms info
Laminopathy type Decaudain-Vigouroux
Atypical Werner syndrome

LMNA LMNA


COMMON
GENES
LMNA



Citations in the biomedical literature:


Laminopathy type Decaudain-Vigouroux
LMNA
Atypical Werner syndrome



Laminopathy type Decaudain-Vigouroux
Atypical Werner syndrome

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

Synonym(s):
- Atypical progeroid syndrome

Classification (Orphanet):
- Rare endocrine disease
- Rare genetic 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:
(no data available)
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.