inborn error of amino acid metabolism pathway
hyperprolinemia type II pathway
1-pyrroline-5-carboxylate dehydrogenase deficiency pathway
2015-09-17T15:25:18Z
A rare condition resulting from alterations in the proline amino acid metabolic pathway leading to high levels of proline and the related compound pyrroline-5-carboxylase in the circulation.
PW:0001932
SMP:00360
VPetri
hyperprolinemia type II disease pathway
pathway