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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H01773 |
4p deletion syndrome Wolf-Hirschhorn syndrome |
4p deletion syndrome, also known as Wolf-Hirschhorn syndrome (WHS), is a congenital disorder associated with various deformities. WHS is caused by deletion of the WHS critical resion (WHSCR) of chromosome ... | Chromosomal abnormality |
CPLX1 [HSA:10815] [KO:K15294] CTBP1 [HSA:1487] [KO:K04496] FGFRL1 [HSA:53834] [KO:K26107] LETM1 [HSA:3954] [KO:K17800] NSD2 [HSA:7468] [KO:K11424] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |