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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H01927 | Van der Woude syndrome | ... allelic syndrome of VWS. These syndromes emanate mainly from etiologic variants in IRF6 gene, though GRHL3 has been shown to be mutated in about 5% of VWS patients that lack etiologic variants in IRF6. ... | Congenital malformation |
(VWS1) IRF6 [HSA:3664] [KO:K10154] (VWS2) GRHL3 [HSA:57822] [KO:K09275] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |