Pathways Knowlegdes
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| Pathway | DOIs | Note |
|---|---|---|
| Homocarnosinosis Accession ID: PathBank:SMP0000385 |
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| Adenosine Deaminase Deficiency Accession ID: PathBank:SMP0000144 |
- | |
| Molybdenum Cofactor Deficiency Accession ID: PathBank:SMP0000203 |
- | |
| 2-Hydroxyglutric Aciduria (D and L Form) Accession ID: PathBank:SMP0000136 |
- | |
| Mercaptopurine Action Pathway Accession ID: PathBank:SMP0000428 |
- | |
| Adenine Phosphoribosyltransferase Deficiency (APRT) Accession ID: PathBank:SMP0000535 |
- | |
| Succinic Semialdehyde Dehydrogenase Deficiency Accession ID: PathBank:SMP0000567 |
- | |
| Purine Nucleotides De Novo Biosynthesis Accession ID: PathBank:SMP0002377 |
- | |
| Hyperinsulinism-Hyperammonemia Syndrome Accession ID: PathBank:SMP0120716 |
- | |
| Lesch-Nyhan Syndrome (LNS) Accession ID: PathBank:SMP0120728 |
- | |
| Molybdenum Cofactor Deficiency Accession ID: PathBank:SMP0120752 |
- | |
| Purine Nucleoside Phosphorylase Deficiency Accession ID: PathBank:SMP0120756 |
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| Xanthinuria Type I Accession ID: PathBank:SMP0120796 |
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| Mitochondrial DNA Depletion Syndrome Accession ID: PathBank:SMP0120820 |
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| 4-Hydroxybutyric Aciduria/Succinic Semialdehyde Dehydrogenase Deficiency Accession ID: PathBank:SMP0120445 |
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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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