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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
4 associated genes
No signs/symptoms info
Laminopathy type Decaudain-Vigouroux
Myoclonus-dystonia syndrome

LMNA DRD2
DYT15
()
SGCE
TOR1A


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
LMNA
(0.75)
TOR1A



Citations in the biomedical literature:


Laminopathy type Decaudain-Vigouroux
LMNA
Myoclonus-dystonia syndrome
DRD2 DYT15 SGCE TOR1A



Laminopathy type Decaudain-Vigouroux
Myoclonus-dystonia syndrome

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

Synonym(s):
- Alcohol-responsive dystonia
- DYT11
- Hereditary essential myoclonus
- Myoclonic dystonia

Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (Orphanet):
- 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:
Class of prevalence: 1-9 / 1 000 000
Average age onset: childhood
Average age of death: normal
Type of inheritance: autosomal dominant

External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: C536096

No signs/symptoms info available.