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Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal recessive myogenic arthrogryposis multiplex congenita
1 associated gene
No signs/symptoms info
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Autosomal recessive myogenic arthrogryposis multiplex congenita

LMNA
(UniProt - OMIM)
 SYNE1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
LMNA
(0.88)
SYNE1


Citations in the biomedical literature:


Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
LMNA
Autosomal recessive myogenic arthrogryposis multiplex congenita
SYNE1



Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Autosomal recessive myogenic arthrogryposis multiplex congenita

Synonym(s):
(no synonyms)

Synonym(s):
- Autosomal recessive myogenic AMC
- SYNE1-related AMC
- SYNE1-related arthrogryposis multiplex congenita
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.