A hereditary disorder characterized by excessive oxalate production, leading to hyperoxaluria.
Comprehensive, easy-to-understand information about this condition
Checking for content...
GLUT1 deficiency syndrome
MONDO:0000188
disorder of glycogen metabolism
MONDO:0002412
G6PD deficiency
MONDO:0005775
hyperinsulinemic hypoglycemia
MONDO:0005803
primary hyperoxaluria type 1
MONDO:0009823
primary hyperoxaluria type 2
MONDO:0009824