5-oxoprolinase deficiency

5-Oxoprolinase deficiency is clinically a very heterogeneous condition characterized by 5-oxoprolinuria.

Also known as: 5-oxoprolinase deficiency, 5-oxoprolinase deficiency (disease), inborn 5-oxoprolinase (ATP-hydrolyzing) activity disorder, inborn error of 5-oxoprolinase (ATP-hydrolyzing) activity, oxoprolinuria due to oxoprolinase deficiency, rare inborn error of 5-oxoprolinase (ATP-hydrolyzing) activity, 5-alpha-oxoprolinase deficiency, OPLAHD

1 clinical trial for this condition and its sub-types, 0 tagged with 5-oxoprolinase deficiency itself.