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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H01290 | Acute recurrent myoglobinuria | ... by inborn errors of glycogenolysis, mitochondrial fatty acid beta-oxidation, and oxidative phosphorylation. It has been reported that mutations in LPIN1 cause recurrent acute myoglobinuria in childhood. | Inherited metabolic disorder | LPIN1 [HSA:23175] [KO:K15728] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |