ODCs

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1 OMIM reference -
2 associated genes
No signs/symptoms info

COMMON GENES: 1

1 OMIM reference -
1 associated gene
8 signs/symptoms

Paroxysmal exertion-induced dyskinesia

Infantile convulsions and choreoathetosis

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

Citations in the biomedical literature:

Paroxysmal exertion-induced dyskinesia		Infantile convulsions and choreoathetosis
	Synonym(s): - DYT18 - Dystonia 18 - PED		Synonym(s): - ICCA syndrome - Paroxysmal kinesigenic dyskinesia and infantile convulsions

	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: Class of prevalence: <1 / 1 000 000 Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant

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

Infantile convulsions and choreoathetosis
	Very frequent - Chorea / athetosis / choreoathetosis / choreic syndrome - EEG anomalies - Hyperkinesia / dyskinesia - Seizures / epilepsy / absences / spasms / status epilepticus Frequent - Ataxia / incoordination / trouble of the equilibrium - Autosomal dominant inheritance - Facial pain / cephalalgia / migraine Occasional - Tics / stereotypias
Paroxysmal exertion-induced dyskinesia
(no data available)