RIBOFLAVIN 5'-PHOSPHATE Pathways

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Displaying pathways 1 – 24 of 161 in total

Arginine and Proline Metabolism
Arginine and Proline Metabolism
beta-Alanine Metabolism
beta-Alanine Metabolism
Pantothenate and CoA Biosynthesis
Pantothenate and CoA Biosynthesis
Riboflavin Metabolism
Riboflavin Metabolism
Vitamin B6 Metabolism
Vitamin B6 Metabolism
Prolidase Deficiency (PD)
Prolidase Deficiency (PD)
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)
GABA-Transaminase Deficiency
GABA-Transaminase Deficiency
Pyrimidine Metabolism
Pyrimidine Metabolism
beta-Ureidopropionase Deficiency
beta-Ureidopropionase Deficiency
UMP Synthase Deficiency (Orotic Aciduria)
UMP Synthase Deficiency (Orotic Aciduria)
Dihydropyrimidinase Deficiency
Dihydropyrimidinase Deficiency
MNGIE (Mitochondrial Neurogastrointestinal Encephalopathy)
MNGIE (Mitochondrial Neurogastrointestinal Encephalopathy)
Carnosinuria, Carnosinemia
Carnosinuria, Carnosinemia
Hypophosphatasia
Hypophosphatasia
Creatine Deficiency, Guanidinoacetate Methyltransferase Deficiency
Creatine Deficiency, Guanidinoacetate Methyltransferase 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

Displaying pathways 1 – 24 of 161 in total