Oxygen Pathways

← Back to Oxygen

Displaying pathways 25 – 48 of 792 in total

Methionine Metabolism
Methionine Metabolism
17-beta Hydroxysteroid Dehydrogenase III Deficiency
17-beta Hydroxysteroid Dehydrogenase III Deficiency
beta-Ketothiolase Deficiency
beta-Ketothiolase Deficiency
2-Methyl-3-hydroxybutyryl-CoA Dehydrogenase Deficiency
2-Methyl-3-hydroxybutyryl-CoA Dehydrogenase Deficiency
Propionic Acidemia
Propionic Acidemia
3-Hydroxy-3-methylglutaryl-CoA Lyase Deficiency
3-Hydroxy-3-methylglutaryl-CoA Lyase Deficiency
Maple Syrup Urine Disease
Maple Syrup Urine Disease
3-Methylcrotonyl-CoA Carboxylase Deficiency Type I
3-Methylcrotonyl-CoA Carboxylase Deficiency Type I
3-Methylglutaconic Aciduria Type I
3-Methylglutaconic Aciduria Type I
3-Methylglutaconic Aciduria Type III
3-Methylglutaconic Aciduria Type III
Methylmalonate Semialdehyde Dehydrogenase Deficiency
Methylmalonate Semialdehyde Dehydrogenase Deficiency
Methylmalonic Aciduria
Methylmalonic Aciduria
Adenosine Deaminase Deficiency
Adenosine Deaminase Deficiency
Adenylosuccinate Lyase Deficiency
Adenylosuccinate Lyase Deficiency
Gout or Kelley-Seegmiller Syndrome
Gout or Kelley-Seegmiller Syndrome
Lesch-Nyhan Syndrome (LNS)
Lesch-Nyhan Syndrome (LNS)
Molybdenum Cofactor Deficiency
Molybdenum Cofactor Deficiency
Xanthine Dehydrogenase Deficiency (Xanthinuria)
Xanthine Dehydrogenase Deficiency (Xanthinuria)
Purine Nucleoside Phosphorylase Deficiency
Purine Nucleoside Phosphorylase Deficiency
AICA-Ribosiduria
AICA-Ribosiduria
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

Displaying pathways 25 – 48 of 792 in total