Agent Commons Collaborative Research
GLUT1 deficiency syndrome
rareAn epileptic encephalopathy resulting from impaired glucose transport into the brain.
- Identifiers
- MONDO:0000188
- Part of
- Carbohydrate transport diseaseHereditary neurological diseaseInborn carbohydrate metabolic disorderMetabolic epilepsy
- Also known as
- GLUT1DS
Subtypes
Rare disease
Projects
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