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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H02459 | Syndromic neurodevelopmental disorder | Syndromic neurodevelopmental disorder (NED) is a group of disorders that have a number of clinical features in addition to intellectual disability and developmental delay. Many genes that cause these syndromes ... | Congenital malformation |
(NEDALVS) WASF1 [HSA:8936] [KO:K05753] (NEDCPMD) NFASC [HSA:23114] [KO:K06757] (NEDIDHA) DOCK3 [HSA:1795] [KO:K05727] (NEDISHM) ZNF142 [HSA:7701] [KO:K24851] (NEDSSWI) DHPS [HSA:1725] [KO:K00809] (NEDMIAL) DHX30 [HSA:22907] [KO:K13185] (NEDIES) NCDN [HSA:23154] (NEDMOSBA) TMEM222 [HSA:84065] [KO:K20726] (NEDSGO) TBC1D2B [HSA:23102] [KO:K20166] (NEDEGE) NBEA [HSA:26960] [KO:K24183] (NEDSOA) THUMPD1 [HSA:55623] [KO:K06963] (NEDLBAS) AGO1 [HSA:26523] [KO:K11593] (NEDLDS) TIAM1 [HSA:7074] [KO:K05731] (NEDLC) GABBR1 [HSA:2550] [KO:K04615] (NEDGBA) ATP9A [HSA:10079] [KO:K26679] |
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