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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H00485 | Robinow syndrome | Robinow syndrome (RS) is a rare genetically heterogeneous condition characterized by hypertelorism, nasal features (large nasal bridge, short upturned nose, and anteverted nares), midface hypoplasia, mesomelic ... | Congenital malformation |
(RRS1) ROR2 [HSA:4920] [KO:K05123] (RRS2) NXN [HSA:64359] [KO:K17609] (DRS1) WNT5A [HSA:7474] [KO:K00444] (DRS2) DVL1 [HSA:1855] [KO:K02353] (DRS3) DVL3 [HSA:1857] [KO:K02353] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |