Pathways Knowlegdes
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| Pathway | DOIs | Note |
|---|---|---|
| Methotrexate Action Pathway Accession ID: PathBank:SMP0000432 |
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| Xanthinuria Type I Accession ID: PathBank:SMP0000512 |
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| Mitochondrial DNA Depletion Syndrome-3 Accession ID: PathBank:SMP0000536 |
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| One Carbon Pool by Folate I Accession ID: PathBank:SMP0002369 |
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| Methionine Metabolism Accession ID: PathBank:SMP0087342 |
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| Purine Metabolism Accession ID: PathBank:SMP0063668 |
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| Adenosine Deaminase Deficiency Accession ID: PathBank:SMP0120669 |
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| AICA-Ribosiduria Accession ID: PathBank:SMP0120673 |
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| Gout or Kelley-Seegmiller Syndrome Accession ID: PathBank:SMP0120709 |
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| Xanthine Dehydrogenase Deficiency (Xanthinuria) Accession ID: PathBank:SMP0120717 |
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| Xanthinuria Type II Accession ID: PathBank:SMP0120797 |
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| Myoadenylate Deaminase Deficiency Accession ID: PathBank:SMP0120821 |
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| Homocystinuria-Megaloblastic Anemia Due to Defect in Cobalamin Metabolism, cblG Complementation Type Accession ID: PathBank:SMP0120853 |
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| Cystathionine beta-Synthase Deficiency Accession ID: PathBank:SMP0120471 |
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| Glycine N-Methyltransferase Deficiency Accession ID: PathBank:SMP0120487 |
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| Methionine Adenosyltransferase Deficiency Accession ID: PathBank:SMP0120519 |
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| S-Adenosylhomocysteine (SAH) Hydrolase Deficiency Accession ID: PathBank:SMP0120527 |
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| Adenine Phosphoribosyltransferase Deficiency (APRT) Accession ID: PathBank:SMP0120600 |
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| Amino Sugar and Nucleotide Sugar Metabolism III Accession ID: PathBank:SMP0121303 |
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| Purine Nucleotides De Novo Biosynthesis Accession ID: PathBank:SMP0121307 |
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