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1 associated gene
No signs/symptoms info
COMMON GENES: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Laminopathy type Decaudain-Vigouroux
Heart-hand syndrome, Slovenian type

LMNA LMNA


COMMON
GENES
LMNA



Citations in the biomedical literature:


Laminopathy type Decaudain-Vigouroux
LMNA
Heart-hand syndrome, Slovenian type



Laminopathy type Decaudain-Vigouroux
Heart-hand syndrome, Slovenian type

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

Synonym(s):
- Atrio-digital dysplasia, Slovenian type
- Cardiac conduction disease - dilated cardiomyopathy - brachydactyly

Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (Orphanet):
- Rare bone disease
- Rare cardiac disease
- Rare developmental defect during embryogenesis
- Rare genetic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

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:
1 OMIM reference -
1 MeSH reference: C535852

No signs/symptoms info available.