xanthinuria pathway
xanthinuria type II pathway
2015-02-09T15:46:28Z
PW:0001592
SMP:00513
VPetri
Xanthinuria is a rare genetic disorder due to alterations in the purine metabolic pathway causing accumulation of xanthine and resulting in a range of symptoms. Of the two types of clinically related disorders, type II is caused by genetic defects in the xanthine dehydrogenase and aldehyde dehydrogenase enzymes.
pathway
xanthinuria disease pathway, type II