An inherited metabolic disease that is has its basis in the disruption of gluconeogenesis.
Comprehensive, easy-to-understand information about this condition
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GLUT1 deficiency syndrome
MONDO:0000188
glucose intolerance
MONDO:0001076
hyperinsulinism
MONDO:0002177
disorder of glycogen metabolism
MONDO:0002412
primary hyperoxaluria
MONDO:0002474
hyperglycemia
MONDO:0002909