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1 associated gene
No signs/symptoms info
COMMON GENES: 1
10 OMIM references -
12 associated genes
No signs/symptoms info
Laminopathy type Decaudain-Vigouroux
Left ventricular noncompaction

LMNA ACTC1
DTNA
LDB3
LMNA
MIB1
MYBPC3
MYH7
MYH7B
PRDM16
TAZ
TNNT2
TPM1


COMMON
GENES
LMNA



Citations in the biomedical literature:


Laminopathy type Decaudain-Vigouroux
LMNA
Left ventricular noncompaction
ACTC1 DTNA LDB3 MIB1 MYBPC3
MYH7 MYH7B PRDM16 TAZ TNNT2 TPM1



Laminopathy type Decaudain-Vigouroux
Left ventricular noncompaction

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

Synonym(s):
- LVNC
- Left ventricular hypertrabeculation
- Spongy myocardium

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

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Diseases of the circulatory system -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant

External references:
No OMIM references
No MeSH references
External references:
10 OMIM references -
No MeSH references

No signs/symptoms info available.