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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H02396 | Corpus callosum agenesis with facial anomalies and cerebellar ataxia | ... syndrome with agenesis of corpus callosum and partial hypoplasia of the vermis and cerebellum. This disease is associated with mutations in FRMD4A, that is involved in cell structure, transport and signaling. | Congenital malformation | FRMD4A [HSA:55691] [KO:K23970] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |