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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H01914 | Christianson syndrome | Christianson syndrome (CS) is a rare, X-linked mental retardation syndrome, caused by mutations in SLC9A6. CS is characterized by severe intellectual disability, microcephaly, epilepsy, ataxia, and absent ... | Congenital malformation | SLC9A6 [HSA:10479] [KO:K12041] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |