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1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
10 OMIM references -
12 associated genes
No signs/symptoms info
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Left ventricular noncompaction

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


COMMON
GENES
LMNA



Citations in the biomedical literature:


Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
LMNA
Left ventricular noncompaction
ACTC1 DTNA LDB3 MIB1 MYBPC3
MYH7 MYH7B PRDM16 TAZ TNNT2 TPM1



Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Left ventricular noncompaction

Synonym(s):
(no synonyms)

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

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

Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the circulatory system -

Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.