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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H00200 | Beta-ureidopropionase deficiency | Deficiency of beta-ureidopropionase which catalyzes the biosynthesis of beta-alanine and the last step in pyrimidine degradation is an autosomal recessive condition associated with neurological and developmental ... | Inherited metabolic disorder | UPB1 [HSA:51733] [KO:K01431] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |