Pathways Knowlegdes
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| Pathway | DOIs | Note |
|---|---|---|
| Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency) Accession ID: PathBank:SMP0120710 |
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| Ornithine Aminotransferase Deficiency (OAT Deficiency) Accession ID: PathBank:SMP0120758 |
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| Hyperornithinemia-Hyperammonemia-Homocitrullinuria [HHH-syndrome] Accession ID: PathBank:SMP0120790 |
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| Creatine Deficiency, Guanidinoacetate Methyltransferase Deficiency Accession ID: PathBank:SMP0120569 |
- | |
| Arginine and Proline Metabolism Accession ID: PathBank:SMP0000020 |
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| Arginine: Glycine Amidinotransferase Deficiency (AGAT Deficiency) Accession ID: PathBank:SMP0000362 |
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| Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency) Accession ID: PathBank:SMP0000188 |
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| Creatine Deficiency, Guanidinoacetate Methyltransferase Deficiency Accession ID: PathBank:SMP0000504 |
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| Arginine and Proline Metabolism Accession ID: PathBank:SMP0063596 |
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| Hyperprolinemia Type II Accession ID: PathBank:SMP0120721 |
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| Prolidase Deficiency (PD) Accession ID: PathBank:SMP0120761 |
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| Hyperornithinemia with Gyrate Atrophy (HOGA) Accession ID: PathBank:SMP0120789 |
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| Hyperprolinemia Type I Accession ID: PathBank:SMP0120499 |
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| Prolinemia Type II Accession ID: PathBank:SMP0120539 |
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| L-Arginine:Glycine Amidinotransferase Deficiency Accession ID: PathBank:SMP0120572 |
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| Prolidase Deficiency (PD) Accession ID: PathBank:SMP0000207 |
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| Prolinemia Type II Accession ID: PathBank:SMP0000208 |
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| L-Arginine:Glycine Amidinotransferase Deficiency Accession ID: PathBank:SMP0000507 |
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| Creatine Deficiency, Guanidinoacetate Methyltransferase Deficiency Accession ID: PathBank:SMP0120788 |
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| Hyperprolinemia Type II Accession ID: PathBank:SMP0120501 |
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