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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H00529 | Cranioectodermal dysplasia | Cranioectodermal dysplasia (CED) is a rare disorder characterized by defects of ectoderm-derived structures with typical craniofacial appearances, skeletal deformities and tubulointerstitial nephritis ... | Congenital malformation |
(CED1) IFT122 [HSA:55764] [KO:K19656] (CED2) WDR35 [HSA:57539] [KO:K19674] (CED3) IFT43 [HSA:112752] [KO:K19675] (CED4) WDR19 [HSA:57728] [KO:K19671] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |