Pentosuria is an inborn error of metabolism which is characterized by the excretion of 1 to 4 g of the pentose L-xylulose in the urine per day.
Comprehensive, easy-to-understand information about this condition
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Gene data from MyGene.info • Click to view on NCBI Gene
anemia, nonspherocytic hemolytic, due to G6PD deficiency
MONDO:0010480
transaldolase deficiency
MONDO:0011624
ribose-5-P isomerase deficiency
MONDO:0012073
transketolase deficiency
MONDO:0014881
isolated sedoheptulokinase deficiency
MONDO:0014969