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

LMNA SYNE1


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Laminopathy type Decaudain-Vigouroux
LMNA
Autosomal recessive myogenic arthrogryposis multiplex congenita
SYNE1



Laminopathy type Decaudain-Vigouroux
Autosomal recessive myogenic arthrogryposis multiplex congenita

Synonym(s):
- Laminopathy with severe metabolic syndrome and myopathy

Synonym(s):
- Autosomal recessive myogenic AMC
- SYNE1-related AMC
- SYNE1-related arthrogryposis multiplex congenita

Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

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.