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Ammonia Pathways
← Back to Ammonia
Displaying pathways
49 – 72
of
277
in total
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Homocarnosinosis
Homocarnosinosis
Hyperinsulinism-Hyperammonemia Syndrome
Hyperinsulinism-Hyperammonemia Syndrome
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
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)
Canavan Disease
Canavan Disease
Hypoacetylaspartia
Hypoacetylaspartia
Cystathionine beta-Synthase Deficiency
Cystathionine beta-Synthase Deficiency
Hypermethioninemia
Hypermethioninemia
S-Adenosylhomocysteine (SAH) Hydrolase Deficiency
S-Adenosylhomocysteine (SAH) Hydrolase Deficiency
Glycine N-Methyltransferase Deficiency
Glycine N-Methyltransferase Deficiency
Methylenetetrahydrofolate Reductase Deficiency (MTHFRD)
Methylenetetrahydrofolate Reductase Deficiency (MTHFRD)
Displaying pathways
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Structure