Pathways Knowlegdes
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| Pathway | DOIs | Note |
|---|---|---|
| Glycine N-Methyltransferase Deficiency Accession ID: PathBank:SMP0120707 |
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| Methionine Adenosyltransferase Deficiency Accession ID: PathBank:SMP0120739 |
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| S-Adenosylhomocysteine (SAH) Hydrolase Deficiency Accession ID: PathBank:SMP0120747 |
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| Adenine Phosphoribosyltransferase Deficiency (APRT) Accession ID: PathBank:SMP0120819 |
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| Folate Malabsorption, Hereditary Accession ID: PathBank:SMP0120875 |
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| Hypermethioninemia Accession ID: PathBank:SMP0120498 |
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| Methylenetetrahydrofolate Reductase Deficiency (MTHFRD) Accession ID: PathBank:SMP0120522 |
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| Polymyxin Resistance Accession ID: PathBank:SMP0122234 |
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| Folate Metabolism Accession ID: PathBank:SMP0000053 |
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| Lesch-Nyhan Syndrome (LNS) Accession ID: PathBank:SMP0000364 |
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| AICA-Ribosiduria Accession ID: PathBank:SMP0000168 |
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| S-Adenosylhomocysteine (SAH) Hydrolase Deficiency Accession ID: PathBank:SMP0000214 |
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| Azathioprine Action Pathway Accession ID: PathBank:SMP0000427 |
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| Homocystinuria-Megaloblastic Anemia Due to Defect in Cobalamin Metabolism, cblG Complementation Type Accession ID: PathBank:SMP0000570 |
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| Folate Malabsorption, Hereditary Accession ID: PathBank:SMP0000724 |
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| Folate Metabolism Accession ID: PathBank:SMP0000801 |
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| Purine Metabolism Accession ID: PathBank:SMP0087239 |
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| Folate Metabolism Accession ID: PathBank:SMP0087295 |
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| Methionine Metabolism Accession ID: PathBank:SMP0087403 |
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| Folate Metabolism Accession ID: PathBank:SMP0087435 |
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