Adenosine-5-phosphate Pathways

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Displaying pathways 1,273 – 1,296 of 1,351 in total

Dimethylglycine Dehydrogenase Deficiency
Dimethylglycine Dehydrogenase Deficiency
Sarcosinemia
Sarcosinemia
Non-Ketotic Hyperglycinemia
Non-Ketotic Hyperglycinemia
3-Phosphoglycerate Dehydrogenase Deficiency
3-Phosphoglycerate Dehydrogenase Deficiency
Phenylketonuria
Phenylketonuria
Tyrosinemia Type 2 (or Richner-Hanhart Syndrome)
Tyrosinemia Type 2 (or Richner-Hanhart Syndrome)
Tyrosinemia Type 3 (TYRO3)
Tyrosinemia Type 3 (TYRO3)
beta-Mercaptolactate-Cysteine Disulfiduria
beta-Mercaptolactate-Cysteine Disulfiduria
Cystinosis, Ocular Nonnephropathic
Cystinosis, Ocular Nonnephropathic
Malonic Aciduria
Malonic Aciduria
Methylmalonic Aciduria Due to Cobalamin-Related Disorders
Methylmalonic Aciduria Due to Cobalamin-Related Disorders
Malonyl-CoA Decarboxylase Deficiency
Malonyl-CoA Decarboxylase Deficiency
Arginine: Glycine Amidinotransferase Deficiency (AGAT Deficiency)
Arginine: Glycine Amidinotransferase Deficiency (AGAT Deficiency)
Hyperprolinemia Type II
Hyperprolinemia Type II
Hyperprolinemia Type I
Hyperprolinemia Type I
Prolinemia Type II
Prolinemia Type II
Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency)
Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency)
Ornithine Aminotransferase Deficiency (OAT Deficiency)
Ornithine Aminotransferase Deficiency (OAT Deficiency)
Hyperornithinemia with Gyrate Atrophy (HOGA)
Hyperornithinemia with Gyrate Atrophy (HOGA)
Hyperornithinemia-Hyperammonemia-Homocitrullinuria (HHH-syndrome)
Hyperornithinemia-Hyperammonemia-Homocitrullinuria (HHH-syndrome)
L-Arginine:Glycine Amidinotransferase Deficiency
L-Arginine:Glycine Amidinotransferase Deficiency
Glucose-6-phosphate Dehydrogenase Deficiency
Glucose-6-phosphate Dehydrogenase Deficiency
Ribose-5-phosphate Isomerase Deficiency
Ribose-5-phosphate Isomerase Deficiency
Transaldolase Deficiency
Transaldolase Deficiency

Displaying pathways 1,273 – 1,296 of 1,351 in total