Oxygen Pathways

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Displaying pathways 49 – 72 of 792 in total

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)
Aromatic L-Aminoacid Decarboxylase Deficiency
Aromatic L-Aminoacid Decarboxylase Deficiency
Isovaleric Aciduria
Isovaleric Aciduria
Canavan Disease
Canavan Disease
Hypoacetylaspartia
Hypoacetylaspartia
Smith-Lemli-Opitz Syndrome (SLOS)
Smith-Lemli-Opitz Syndrome (SLOS)
CHILD Syndrome
CHILD Syndrome
Desmosterolosis
Desmosterolosis
Chondrodysplasia Punctata II, X-Linked Dominant (CDPX2)
Chondrodysplasia Punctata II, X-Linked Dominant (CDPX2)
Lysosomal Acid Lipase Deficiency (Wolman Disease)
Lysosomal Acid Lipase Deficiency (Wolman Disease)
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)
Methionine Adenosyltransferase Deficiency
Methionine Adenosyltransferase Deficiency
GABA-Transaminase Deficiency
GABA-Transaminase Deficiency
Glutaric Aciduria Type I
Glutaric Aciduria Type I
Saccharopinuria/Hyperlysinemia II
Saccharopinuria/Hyperlysinemia II
Histidinemia
Histidinemia
Leukotriene C4 Synthesis Deficiency
Leukotriene C4 Synthesis Deficiency
Tyrosinemia Type 2 (or Richner-Hanhart Syndrome)
Tyrosinemia Type 2 (or Richner-Hanhart Syndrome)

Displaying pathways 49 – 72 of 792 in total