Cytoscape Web
Click node...

Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Paroxysmal exertion-induced dyskinesia
1 OMIM reference -
2 associated genes
No signs/symptoms info
Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity
Paroxysmal exertion-induced dyskinesia

SLC2A1
(UniProt - OMIM)
 PRRT2
(UniProt - OMIM)
SLC2A1
(UniProt - OMIM)

COMMON
GENES 		SLC2A1


Citations in the biomedical literature:


Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity
SLC2A1
Paroxysmal exertion-induced dyskinesia
PRRT2



Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity
Paroxysmal exertion-induced dyskinesia

Synonym(s):
- DYT9
- Episodic choreoathetosis/spasticity
Synonym(s):
- DYT18
- Dystonia 18
- PED
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.