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Paroxysmal exertion-induced dyskinesia
1 OMIM reference -
2 associated genes
14 connected diseases
No signs/symptoms info
Disease Type of connection
Benign familial infantile seizures
Childhood absence epilepsy
Encephalopathy due to GLUT1 deficiency
Epilepsy with myoclonic-astatic seizures
Familial or sporadic hemiplegic migraine
Hereditary cryohydrocytosis with reduced stomatin
Infantile convulsions and choreoathetosis
Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity
Paroxysmal kinesigenic dyskinesia
Paroxysmal non-kinesigenic dyskinesia
Essential thrombocythemia
Myelofibrosis with myeloid metaplasia
Chuvash erythrocytosis
Von Hippel-Lindau disease
Synonym(s):
- DYT18
- Dystonia 18
- PED
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
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
Gene symbol UniProt reference OMIM reference
PRRT2 Q7Z6L0614386
SLC2A1 P11166138140
No signs/symptoms info available.