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

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

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


Citations in the biomedical literature:


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



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

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