An inherited metabolic disease that is has its basis in the disruption of glucose transport.
Comprehensive, easy-to-understand information about this condition
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GLUT1 deficiency syndrome
MONDO:0000188
congenital sucrase-isomaltase deficiency
MONDO:0009114
congenital lactase deficiency
MONDO:0009115
familial renal glucosuria
MONDO:0009297
free sialic acid storage disease, infantile form
MONDO:0010027
dystonia 9
MONDO:0010983