NADH Pathways

Pterine Biosynthesis

Tyrosine Metabolism

Porphyrin Metabolism

Retinol Metabolism

Acute Intermittent Porphyria

Porphyria Variegata (PV)

Congenital Erythropoietic Porphyria (CEP) or Gunther Disease

Alkaptonuria

Hawkinsinuria

Tyrosinemia Type I

Vitamin A Deficiency

Hereditary Coproporphyria (HCP)

Disulfiram Action Pathway

DOPA-Responsive Dystonia

Hyperphenylalaninemia Due to Guanosine Triphosphate Cyclohydrolase Deficiency

Hyperphenylalaninemia Due to 6-Pyruvoyltetrahydropterin Synthase Deficiency (ptps)

Hyperphenylalaninemia Due to DHPR-Deficiency

Segawa Syndrome

Sepiapterin Reductase Deficiency

Tyrosinemia, Transient, of the Newborn

Dopamine beta-Hydroxylase Deficiency

Monoamine Oxidase-A Deficiency (MAO-A)

Homocystinuria-Megaloblastic Anemia Due to Defect in Cobalamin Metabolism, cblG Complementation Type

Felbamate Metabolism Pathway