Carbon dioxide Pathways

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Displaying pathways 73 – 96 of 4,254 in total

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
Ethylmalonic Encephalopathy
Ethylmalonic Encephalopathy
Glutaric Aciduria Type I
Glutaric Aciduria Type I
Short-Chain Acyl-CoA Dehydrogenase Deficiency (SCAD Deficiency)
Short-Chain Acyl-CoA Dehydrogenase Deficiency (SCAD Deficiency)
GABA-Transaminase Deficiency
GABA-Transaminase Deficiency
Glutaric Aciduria Type I
Glutaric Aciduria Type I
Saccharopinuria/Hyperlysinemia II
Saccharopinuria/Hyperlysinemia II
Histidinemia
Histidinemia
Leigh Syndrome
Leigh Syndrome
Pyruvate Decarboxylase E1 Component Deficiency (PDHE1 Deficiency)
Pyruvate Decarboxylase E1 Component Deficiency (PDHE1 Deficiency)
Pyruvate Dehydrogenase Complex Deficiency
Pyruvate Dehydrogenase Complex Deficiency
Tyrosinemia Type 2 (or Richner-Hanhart Syndrome)
Tyrosinemia Type 2 (or Richner-Hanhart Syndrome)
Tyrosinemia Type 3 (TYRO3)
Tyrosinemia Type 3 (TYRO3)
Refsum Disease
Refsum Disease

Displaying pathways 73 – 96 of 4,254 in total