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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H00178 | Glutaric acidemia | Glutaric aciduria type I (GA1) is an autosomal recessive disorder resulting from a deficiency of glutaryl-CoA dehydrogenase leading to an accumulation of glutaric and 3-hydroxyglutaric acids and secondary ... | Inherited metabolic disorder |
(GA1) GCDH [HSA:2639] [KO:K00252] (GA2) ETFA [HSA:2108] [KO:K03522] (GA2) ETFB [HSA:2109] [KO:K03521] (GA2) ETFDH [HSA:2110] [KO:K00311] (GA3) SUGCT [HSA:79783] [KO:K18703] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |