Support By : Li-lab
| PATHWAY_NAME | REACTOME_ID | KEGG_ID | DRUG_NAME | PUBCHEM_CID | Datasource |
|---|---|---|---|---|---|
| MPS II - Hunter syndrome | R-HSA-2206296 | 0 | Water | 443935 | pubchem |
| MPS IIIA - Sanfilippo syndrome A | R-HSA-2206307 | 0 | Water | 443935 | pubchem |
| MPS IIIB - Sanfilippo syndrome B | R-HSA-2206282 | 0 | Water | 443935 | pubchem |
| MPS IIID - Sanfilippo syndrome D | R-HSA-2206305 | 0 | Water | 443935 | pubchem |
| MPS IV - Morquio syndrome A | R-HSA-2206290 | 0 | Water | 443935 | pubchem |
| MPS IV - Morquio syndrome B | R-HSA-2206290 | 0 | Water | 443935 | pubchem |
| MPS VI - Maroteaux-Lamy syndrome | R-HSA-2206285 | 0 | Water | 443935 | pubchem |
| MPS VII - Sly syndrome | R-HSA-2206292 | 0 | Water | 443935 | pubchem |
| MPS IX - Natowicz syndrome | R-HSA-2206280 | 0 | Water | 443935 | pubchem |
| Glycogen storage diseases | R-HSA-3229121 | 0 | Water | 443935 | pubchem |
| GSD Ia | R-HSA-3274531 | 0 | Water | 443935 | pubchem |
| GSD II | R-ALL-1973971 | 0 | Water | 443935 | pubchem |
| Myoclonic epilepsy of Lafora | R-HSA-3785653 | 0 | Water | 443935 | pubchem |
| Severe congenital neutropenia type 4 | #N/A | #N/A | Water | 443935 | pubchem |
| Intestinal saccharidase deficiencies | R-HSA-5659898 | 0 | Water | 443935 | pubchem |
| Defects in vitamin and cofactor metabolism | R-HSA-3296482 | 0 | Water | 443935 | pubchem |
| Defects in cobalamin metabolism | R-HSA-3296469 | 0 | Water | 443935 | pubchem |
| Metabolic disorders of biological oxidation enzymes | 0 | 0 | Water | 443935 | pubchem |
| Defective ACY1 causes encephalopathy | R-HSA-5579007 | 0 | Water | 443935 | pubchem |
| Defective AHCY causes HMAHCHD | R-HSA-5578997 | 0 | Water | 443935 | pubchem |