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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H02057 | Rotor syndrome | ... coproporphyrinuria, and near-absent hepatic uptake of anionic diagnostics. It is linked to mutations predicted to cause complete deficiencies of the organic anion transporting polypeptides OATP1B1 and OATP1B3. | Inherited metabolic disorder |
SLCO1B1 [HSA:10599] [KO:K05043] SLCO1B3 [HSA:28234] [KO:K05043] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |