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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H00440 | Rett syndrome | ... stereotypical hand movements. Mutations in MECP2 are identified in most patients with classic Rett syndrome. Recently, mutations in FOXG1 gene have been shown to cause congenital variant of Rett syndrome. | Nervous system disease |
MECP2 [HSA:4204] [KO:K11588] FOXG1 [HSA:2290] [KO:K09385] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |