GTP cyclohydrolase I deficiency with hyperphenylalaninemia
MONDO:0100186Also known as: GTPCH deficiency, hyperphenylalaninemia due to GTP cyclohydrolase deficiency, hyperphenylalaninemia, Bh4-deficient, type B, GTP cyclohydrolase 1 deficiency, GTP cyclohydrolase I deficiency, HPABH4B, hyperphenylalaninemia, BH4-deficient, B, hyperphenylalaninemia, tetrahydrobiopterin-deficient, due to GTP cyclohydrolase 1 deficiency
0 clinical trials for this condition and its sub-types, 0 tagged with GTP cyclohydrolase I deficiency with hyperphenylalaninemia itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.