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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H01237 | Sulfite oxidase deficiency | Sulfite oxidase deficiency is a rare inherited disease with severe neurological symptoms such as intractable neonatal or infantile seizures, hypotonia or hypertonia, feeding difficulties, profound developmental ... | Inherited metabolic disorder | (ISOD) SUOX [HSA:6821] [KO:K00387] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |