ODCs

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

COMMON GENES: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Paroxysmal exertion-induced dyskinesia

Encephalopathy due to GLUT1 deficiency

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

Citations in the biomedical literature:

Paroxysmal exertion-induced dyskinesia		Encephalopathy due to GLUT1 deficiency
	Synonym(s): - DYT18 - Dystonia 18 - PED		Synonym(s): - De Vivo disease - Glucose transporter type 1 deficiency - Glut-1 deficiency Syndrome - Glut1-DS

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Inborn errors of metabolism - 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: no data available 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.