ODCs

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

COMMON GENES: 1

3 associated genes
No signs/symptoms info

Encephalopathy due to GLUT1 deficiency

Epilepsy with myoclonic-astatic seizures

Citations in the biomedical literature:

Encephalopathy due to GLUT1 deficiency		Epilepsy with myoclonic-astatic seizures
	Synonym(s): - De Vivo disease - Glucose transporter type 1 deficiency - Glut-1 deficiency Syndrome - Glut1-DS		Synonym(s): - Doose syndrome - EMAS - Epilepsy with myoclonic-atonic seizures - MAE - Myoclonic atonic epilepsy - Myoclonic-astatic epilepsy in early childhood

	Classification (Orphanet): - Inborn errors of metabolism - 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: unknown Average age onset: neonatal/infancy Average age of death: no data available Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: unknown

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

No signs/symptoms info available.