Inborn disorder of ornithine, proline and hydroxyproline metabolism

MONDO:0800156

A disorder of amino acid metabolism that has its basis in the disruption of the metabolism of ornithine, proline and/or hydroxyproline.

0 clinical trials for this condition and its sub-types, 0 tagged with Inborn disorder of ornithine, proline and hydroxyproline metabolism itself.

Where it sits in the disease tree

Part of

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.