Carbon dioxide Pathways

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Displaying pathways 169 – 192 of 4,254 in total

Galactosemia III
Galactosemia III
Tyrosine Hydroxylase Deficiency
Tyrosine Hydroxylase Deficiency
Dopamine beta-Hydroxylase Deficiency
Dopamine beta-Hydroxylase Deficiency
Malonyl-CoA Decarboxylase Deficiency
Malonyl-CoA Decarboxylase Deficiency
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
Cholesteryl Ester Storage Disease
Cholesteryl Ester Storage Disease
Hyper-IgD Syndrome
Hyper-IgD Syndrome
Mevalonic Aciduria
Mevalonic Aciduria
Wolman Disease
Wolman Disease
Xanthinuria Type I
Xanthinuria Type I
Xanthinuria Type II
Xanthinuria Type II
Glucose-6-phosphate Dehydrogenase Deficiency
Glucose-6-phosphate Dehydrogenase Deficiency
Ribose-5-phosphate Isomerase Deficiency
Ribose-5-phosphate Isomerase Deficiency
Transaldolase Deficiency
Transaldolase Deficiency
3-Hydroxyisobutyric Acid Dehydrogenase Deficiency
3-Hydroxyisobutyric Acid Dehydrogenase Deficiency
3-Hydroxyisobutyric Aciduria
3-Hydroxyisobutyric Aciduria
Isobutyryl-CoA Dehydrogenase Deficiency
Isobutyryl-CoA Dehydrogenase Deficiency
Isovaleric Acidemia
Isovaleric Acidemia
Fabry Disease
Fabry Disease
Krabbe Disease
Krabbe Disease
Hyperlysinemia I, Familial
Hyperlysinemia I, Familial

Displaying pathways 169 – 192 of 4,254 in total