Pathways Knowlegdes
Biological pathway database
| Pathway | DOIs | Note |
|---|---|---|
| Adenylosuccinate Lyase Deficiency Accession ID: PathBank:SMP0000167 |
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| Xanthine Dehydrogenase Deficiency (Xanthinuria) Accession ID: PathBank:SMP0000220 |
- | |
| Xanthinuria Type I Accession ID: PathBank:SMP0000512 |
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| Mitochondrial DNA Depletion Syndrome-3 Accession ID: PathBank:SMP0000536 |
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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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| Adenine Phosphoribosyltransferase Deficiency (APRT) Accession ID: PathBank:SMP0120600 |
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| Purine Metabolism Accession ID: PathBank:SMP0000050 |
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| Adenosine Deaminase Deficiency Accession ID: PathBank:SMP0000144 |
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| Molybdenum Cofactor Deficiency Accession ID: PathBank:SMP0000203 |
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| Mercaptopurine Action Pathway Accession ID: PathBank:SMP0000428 |
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| Adenine Phosphoribosyltransferase Deficiency (APRT) Accession ID: PathBank:SMP0000535 |
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| Lesch-Nyhan Syndrome (LNS) Accession ID: PathBank:SMP0120728 |
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| Molybdenum Cofactor Deficiency Accession ID: PathBank:SMP0120752 |
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| Purine Nucleoside Phosphorylase Deficiency Accession ID: PathBank:SMP0120756 |
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