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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H00179 | 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency | 3-Hydroxy-3-methylglutaryl-CoA lyase (HL) deficiency is a rare autosomal recessive genetic disorder characterized by recurrent episodes of metabolic acidosis, hyperammonemia without ketosis, hypoglycemia ... | Inherited metabolic disorder | HMGCL [HSA:3155] [KO:K01640] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |