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1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Charcot-Marie-Tooth disease type 2B1

LMNA LMNA


COMMON
GENES
LMNA



Citations in the biomedical literature:


Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
LMNA
Charcot-Marie-Tooth disease type 2B1



Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Charcot-Marie-Tooth disease type 2B1

Synonym(s):
(no synonyms)

Synonym(s):
- AR-CMT2B1
- Autosomal recessive Charcot-Marie-Tooth disease type 2B1
- Autosomal recessive axonal CMT4C1

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

Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the nervous 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: childhood
Average age of death: -
Type of inheritance: autosomal recessive

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: C537990

No signs/symptoms info available.