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Autosomal recessive myogenic arthrogryposis multiplex congenita
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Laminopathy type Decaudain-Vigouroux
1 associated gene
No signs/symptoms info
Autosomal recessive myogenic arthrogryposis multiplex congenita
Laminopathy type Decaudain-Vigouroux

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
Laminopathy type Decaudain-Vigouroux
LMNA



Autosomal recessive myogenic arthrogryposis multiplex congenita
Laminopathy type Decaudain-Vigouroux

Synonym(s):
- Autosomal recessive myogenic AMC
- SYNE1-related AMC
- SYNE1-related arthrogryposis multiplex congenita
Synonym(s):
- Laminopathy with severe metabolic syndrome and myopathy
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.