Pathways Knowlegdes
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| Pathway | DOIs | Note |
|---|---|---|
| Mitochondrial DNA Depletion Syndrome Accession ID: PathBank:SMP0120820 |
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| Adenylosuccinate Lyase Deficiency Accession ID: PathBank:SMP0120449 |
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| Gout or Kelley-Seegmiller Syndrome Accession ID: PathBank:SMP0120489 |
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| Xanthine Dehydrogenase Deficiency (Xanthinuria) Accession ID: PathBank:SMP0120497 |
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| Xanthinuria Type II Accession ID: PathBank:SMP0120578 |
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| Myoadenylate Deaminase Deficiency Accession ID: PathBank:SMP0120602 |
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| Homocystinuria-Megaloblastic Anemia Due to Defect in Cobalamin Metabolism, cblG Complementation Type Accession ID: PathBank:SMP0120634 |
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| Gout or Kelley-Seegmiller Syndrome Accession ID: PathBank:SMP0000365 |
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| Purine Nucleoside Phosphorylase Deficiency Accession ID: PathBank:SMP0000210 |
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| Hypermethioninemia Accession ID: PathBank:SMP0000341 |
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| Methionine Adenosyltransferase Deficiency Accession ID: PathBank:SMP0000221 |
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| Thioguanine Action Pathway Accession ID: PathBank:SMP0000430 |
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| Xanthinuria Type II Accession ID: PathBank:SMP0000513 |
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| Myoadenylate Deaminase Deficiency Accession ID: PathBank:SMP0000537 |
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| Glycine Metabolism Accession ID: PathBank:SMP0002320 |
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| Tetrahydrofolate Biosynthesis Accession ID: PathBank:SMP0002334 |
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| Serine Metabolism Accession ID: PathBank:SMP0002443 |
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| Purine Metabolism Accession ID: PathBank:SMP0087332 |
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| Folate Metabolism Accession ID: PathBank:SMP0087380 |
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| Cystathionine beta-Synthase Deficiency Accession ID: PathBank:SMP0120691 |
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