ODCs

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

COMMON GENES: 1

2 OMIM references -
1 associated gene
No signs/symptoms info

Paroxysmal exertion-induced dyskinesia

Paroxysmal kinesigenic dyskinesia

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

Citations in the biomedical literature:

Paroxysmal exertion-induced dyskinesia		Paroxysmal kinesigenic dyskinesia
	Synonym(s): - DYT18 - Dystonia 18 - PED		Synonym(s): - Familial PKD - Familial paroxysmal kinesigenic dyskinesia - Paroxysmal kinesigenic choreathetosis

	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: 1-9 / 1 000 000 Average age onset: variable Average age of death: normal Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 2 OMIM references - No MeSH references

No signs/symptoms info available.