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Acute encephalopathy with biphasic seizures and late reduced diffusion
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Myoclonus-dystonia syndrome
1 OMIM reference -
4 associated genes
No signs/symptoms info
Acute encephalopathy with biphasic seizures and late reduced diffusion
Myoclonus-dystonia syndrome

ADORA2A
(UniProt - OMIM)
 DRD2
(UniProt - OMIM)
DYT15
()
SGCE
(UniProt - OMIM)
TOR1A
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ADORA2A
(0.89)
DRD2


Citations in the biomedical literature:


Acute encephalopathy with biphasic seizures and late reduced diffusion
ADORA2A
Myoclonus-dystonia syndrome
DRD2 DYT15 SGCE TOR1A



Acute encephalopathy with biphasic seizures and late reduced diffusion
Myoclonus-dystonia syndrome

Synonym(s):
- AESD
- AIEF
- Acute infantile encephalopathy predominantly affecting the frontal lobes
Synonym(s):
- Alcohol-responsive dystonia
- DYT11
- Hereditary essential myoclonus
- Myoclonic dystonia
Classification (Orphanet):
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
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.