Summary

Gtp Cyclohydrolase I Deficiency, also known as hyperphenylalaninemia, bh4-deficient, b,is related to hyperphenylalaninemia, bh4-deficient, b and gtp cyclohydrolase 1-deficient dopa-responsive dystonia,and has symptoms including lethargy, lethargy and muscle rigidity. An important gene associated with Gtp Cyclohydrolase I Deficiency is GCH1 (GTP Cyclohydrolase 1)

All SNPs

Disease Hierarchy

Disease Interacts with Genes

Disease Interacts with Substances

Processes Associated With Trait

Pathways Associated With Trait