complex neurodevelopmental disorder

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
complex neurodevelopmental disorder
TRMT1 Unknown — ClinGen
YWHAZ Unknown — ClinGen
YY1 Unknown — ClinGen
ZBTB18 Unknown — ClinGen —
ZMIZ1 Unknown — ClinGen —
ZNF292 Unknown — ClinGen —
All118 Causal12 Unknown106
Related Diseases Diseases that share the most curated genes with complex neurodevelopmental disorder.
5 View disease cluster →
Non-specific syndromic intellectual disability 105 shared genesCHD8, GABRD, HNRNPU, CACNA1D, CHD2, CNTNAP2, CUL3, DLGAP2, EPB41L1, GIGYF1, GNB2, GRIA1 +93 more Related via 105 shared genes including CHD8, GABRD, HNRNPU. Neurodevelopmental disorder 113 shared genesCHD8, GABRD, HNRNPU, CACNA1D, CHD2, CNTNAP2, CUL3, DLGAP2, EPB41L1, GIGYF1, GNB2, GRIA1 +101 more Related via 113 shared genes including CHD8, GABRD, HNRNPU. Nonsyndromic intellectual disability 26 shared genesEPB41L1, GRIA1, GRIK2, GRIN2B, KCNQ2, NBEA, PRICKLE2, SCN8A, ST3GAL3, ZNF292, CIC, RSRC1 +14 more Related via 26 shared genes including EPB41L1, GRIA1, GRIK2. Developmental and epileptic encephalopathy 29 shared genesGABRD, HNRNPU, CHD2, CNTNAP2, GRIN2B, KCNQ2, MEF2C, NRXN2, SCN8A, ST3GAL3, GRIN2A, KCNB1 +17 more Related via 29 shared genes including GABRD, HNRNPU, CHD2. Intellectual developmental disorder 79 shared genesCHD8, HNRNPU, CACNA1D, CHD2, CNTNAP2, CUL3, EPB41L1, GRIA1, GRIK2, GRIN2B, KCNQ2, KMT5B +67 more Related via 79 shared genes including CHD8, HNRNPU, CACNA1D.