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1 associated gene
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 1
4 OMIM references -
4 associated genes
No signs/symptoms info
Laminopathy type Decaudain-Vigouroux
Autosomal dominant Emery-Dreifuss muscular dystrophy

LMNA LMNA
SYNE1
SYNE2
TMEM43


COMMON
GENES
LMNA


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 dominant Emery-Dreifuss muscular dystrophy
SYNE1 SYNE2 TMEM43



Laminopathy type Decaudain-Vigouroux
Autosomal dominant Emery-Dreifuss muscular dystrophy

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

Synonym(s):
(no synonyms)

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

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

External references:
No OMIM references
No MeSH references
External references:
4 OMIM references -
No MeSH references

No signs/symptoms info available.