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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H00162 | Sjogren-Larsson syndrome | Sjogren-Larsson syndrome is an autosomal recessive neurocutaneous disorder caused by deficiency of microsomal fatty aldehyde dehydrogenase in fatty alcohol metabolism and characterized by congenital ichthyosis | Inherited metabolic disorder | ALDH3A2 [HSA:224] [KO:K00128] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |