Pathways Knowlegdes
Biological pathway database
| Pathway | DOIs | Note |
|---|---|---|
| Myoadenylate Deaminase Deficiency Accession ID: PathBank:SMP0120821 |
- | |
| Adenine Phosphoribosyltransferase Deficiency (APRT) Accession ID: PathBank:SMP0120600 |
- | |
| Purine Metabolism Accession ID: PathBank:SMP0000050 |
- | |
| Adenosine Deaminase Deficiency Accession ID: PathBank:SMP0000144 |
- | |
| Molybdenum Cofactor Deficiency Accession ID: PathBank:SMP0000203 |
- | |
| Mercaptopurine Action Pathway Accession ID: PathBank:SMP0000428 |
- | |
| Adenine Phosphoribosyltransferase Deficiency (APRT) Accession ID: PathBank:SMP0000535 |
- | |
| Lesch-Nyhan Syndrome (LNS) Accession ID: PathBank:SMP0120728 |
- | |
| Molybdenum Cofactor Deficiency Accession ID: PathBank:SMP0120752 |
- | |
| Purine Nucleoside Phosphorylase Deficiency Accession ID: PathBank:SMP0120756 |
- | |
| Xanthinuria Type I Accession ID: PathBank:SMP0120796 |
- | |
| Mitochondrial DNA Depletion Syndrome Accession ID: PathBank:SMP0120820 |
- | |
| Adenylosuccinate Lyase Deficiency Accession ID: PathBank:SMP0120449 |
- | |
| Gout or Kelley-Seegmiller Syndrome Accession ID: PathBank:SMP0120489 |
- | |
| Xanthine Dehydrogenase Deficiency (Xanthinuria) Accession ID: PathBank:SMP0120497 |
- | |
| Xanthinuria Type II Accession ID: PathBank:SMP0120578 |
- | |
| Myoadenylate Deaminase Deficiency Accession ID: PathBank:SMP0120602 |
- | |
| Gout or Kelley-Seegmiller Syndrome Accession ID: PathBank:SMP0000365 |
- | |
| Purine Nucleoside Phosphorylase Deficiency Accession ID: PathBank:SMP0000210 |
- | |
| Thioguanine Action Pathway Accession ID: PathBank:SMP0000430 |
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