Support By : Li-lab
| PATHWAY_NAME | REACTOME_ID | KEGG_ID | DRUG_NAME | PUBCHEM_CID | Datasource |
|---|---|---|---|---|---|
| Hawkinsinuria | 0 | 0 | Fe2+ | 439260 | smpdb |
| beta-Ureidopropionase Deficiency | R-HSA-5602680 | 0 | Fe2+ | 439260 | smpdb |
| Hyper-IgD Syndrome | R-HSA-2206302 | 0 | Fe2+ | 439260 | smpdb |
| Taurine and Hypotaurine Metabolism | R-HSA-1655443 | map00430 | Fe2+ | 439260 | smpdb |
| Tyrosine Metabolism | R-HSA-8963691 | map00350 | Fe2+ | 439260 | smpdb |
| Tyrosinemia, Transient, of the Newborn | R-HSA-5683209 | 0 | Fe2+ | 439260 | smpdb |
| Transaldolase Deficiency | R-HSA-8950367 | 0 | Fe2+ | 439260 | smpdb |
| Alendronate Action Pathway | R-ALL-9717824 | 0 | Fe2+ | 439260 | smpdb |
| Pravastatin Action Pathway | R-ALL-9705578 | 0 | Fe2+ | 439260 | smpdb |
| Disulfiram Action Pathway | R-ALL-9693326 | 0 | Fe2+ | 439260 | smpdb |
| Nucleotide Sugars Metabolism | R-HSA-727802 | 0 | Fe2+ | 439260 | smpdb |
| Dopamine beta-Hydroxylase Deficiency | R-HSA-390651 | 0 | Fe2+ | 439260 | smpdb |
| Steroid Biosynthesis | R-ALL-9841230 | map00100 | Fe2+ | 439260 | smpdb |
| Hypercholesterolemia | R-HSA-9737780 | 0 | Fe2+ | 439260 | smpdb |
| Galactosemia II | R-ALL-1973971 | 0 | Fe2+ | 439260 | smpdb |
| Hereditary Coproporphyria | R-HSA-5657560 | 0 | Fe2+ | 439260 | smpdb |
| GLUT-1 Deficiency Syndrome | R-HSA-5619043 | 0 | Fe2+ | 439260 | smpdb |
| Phenylalanine and Tyrosine Metabolism | R-HSA-8963691 | 0 | Fe2+ | 439260 | smpdb |
| Acute Intermittent Porphyria | Q9NX94 | 0 | Fe2+ | 439260 | smpdb |
| The Oncogenic Action of Succinate | R-HSA-6802957 | 0 | Fe2+ | 439260 | smpdb |