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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H02268 | Wieacker-Wolff syndrome | ... of the feet at birth, muscle atrophy, dyspraxia of the eye, face, and tongue muscles, and mental retardation. WRWF is caused by mutations in the ZC4H2 gene, that is involved in human brain development. | Musculoskeletal disease | ZC4H2 [HSA:55906] [KO:K24369] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |