Intellectual developmental disorder

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This page as CSV This page as PDF All 429 genes as CSV All 429 genes as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
INTELLECTUAL DISABILITY
C3714756MESH:D008607
KDM5A Causal
21937992
CTD, Disgenet
KDM5C Causal
21076407
CTD, Disgenet
KDM6B Causal
21937992
CTD
KIAA0586 Causal — Disgenet —
KIF1C Causal — Disgenet
KIF5B Causal — Disgenet
KLHL20 Causal — Disgenet
KMT2A Causal — Disgenet
KMT2C Causal — Disgenet
KMT2D Causal — Disgenet
KMT2E Causal — Disgenet
KMT5B Causal — Disgenet
L1CAM Causal — Disgenet
LAMB1 Causal — Disgenet
LARP7 Causal
21937992
CTD, Disgenet —
LINS1 Causal
21937992
CTD, Disgenet —
LYSET Causal — Disgenet —
MAGEL2 Causal — Disgenet —
MAN2B1 Causal — Disgenet
MAPK1 Causal — Disgenet
EGFR tyrosine kinase inhibitor resistance Endocrine resistance Platinum drug resistance +161 more
MBD5 Causal — Disgenet
MBOAT7 Causal — Disgenet
MDGA2 Causal — Disgenet
MECP2 Causal
19921286 20098342
CTD, Disgenet
MED12 Causal — Disgenet
MED12L Causal — Disgenet
MED13L Causal
21937992
CTD, Disgenet
MED23 Causal — Disgenet
MEF2C Causal
20412115
CTD, Disgenet
METAP1 Causal — Disgenet
METTL23 Causal
24626631
CTD, Disgenet —
MLYCD Causal — Disgenet
MPZ Causal — Disgenet
MSL3 Causal
30224647
Disgenet
MTOR Causal — Disgenet
EGFR tyrosine kinase inhibitor resistance Endocrine resistance ErbB signaling pathway +61 more
MTR Causal — Disgenet
MTSS2 Causal — Disgenet —
MYT1 Causal — Disgenet —
MYT1L Causal — Disgenet —
NAA10 Causal — Disgenet —
NAA15 Causal
28191889
CTD, Disgenet —
NAGLU Causal
21937992
CTD, Disgenet
NALCN Causal — Disgenet
NBEA Causal — Disgenet —
NCKAP1 Causal — Disgenet
NEDD4L Causal — Disgenet
NEXMIF Causal — Disgenet —
NF1 Causal
21236316
CTD, Disgenet
NFIB Causal — Disgenet —
NFIX Causal — Disgenet —
INTELLECTUAL DISABILITY, AUTOSOMAL DOMINANT 1
MONDO:0007974
MBD5 Causal
23422940 23587880
ClinVar, GWAS catalog
INTELLECTUAL DISABILITY, AUTOSOMAL DOMINANT 39
MONDO:0014678
MYT1L Causal
28859103 34748075 32065501 33622623 30796847
ClinVar, GWAS catalog —
INTELLECTUAL DISABILITY, AUTOSOMAL DOMINANT 50
MONDO:0030916
NAA15 Causal — ClinVar, GenCC —
INTELLECTUAL DISABILITY, AUTOSOMAL DOMINANT 51
MONDO:0030917
KMT5B Causal
29276005 28135719
ClinVar, GWAS catalog
INTELLECTUAL DISABILITY, AUTOSOMAL RECESSIVE 18
MONDO:0013651
MED23 Causal
21868677 25845469 27311965 27457812 30847200
ClinVar, GWAS catalog
INTELLECTUAL DISABILITY, AUTOSOMAL RECESSIVE 27
MONDO:0013702
LINS1 Causal
21937992 23773660 25356970
ClinVar, GWAS catalog —
INTELLECTUAL DISABILITY, AUTOSOMAL RECESSIVE 44
MONDO:0014409
METTL23 Causal
32067349 24501276 24626631
ClinVar, GWAS catalog —
INTELLECTUAL DISABILITY, AUTOSOMAL RECESSIVE 57
MONDO:0014962
MBOAT7 Causal
27616480 30701556
CTD, ClinVar
All809 Causal429 Unknown517
Related Diseases Diseases that share the most curated genes with Intellectual developmental disorder.
5 View disease cluster →
Neurodevelopmental disorder 354 shared genesCHD8, FOXG1, UBE3A, CHRNA7, SIN3A, USP7, ANKRD11, RAI1, BPTF, PSMD12, NFIX, SKI +342 more Related via 354 shared genes including CHD8, FOXG1, UBE3A. Global developmental delay 191 shared genesFOXG1, UBE3A, ANKRD11, KANSL1, BPTF, NFIX, SHANK3, WWOX, PTEN, ACTL6A, ADNP, VCP +179 more Related via 191 shared genes including FOXG1, UBE3A, ANKRD11. Non-specific syndromic intellectual disability 154 shared genesCHD8, CHRNA7, PSMD12, HNRNPU, JMJD1C, ACTL6A, VCP, CACNA1D, ACTL6B, ANK3, CAMK4, CAPZA2 +142 more Related via 154 shared genes including CHD8, CHRNA7, PSMD12. Autism 261 shared genesSOX5, CHD8, FOXG1, UBE3A, CHRNA7, SIN3A, ANKRD11, RAI1, NF1, KANSL1, NFIX, JMJD1C +249 more Related via 261 shared genes including SOX5, CHD8, FOXG1. Nonsyndromic intellectual disability 90 shared genesCDH15, CLIP1, CRADD, CRBN, CUX1, DEAF1, EPB41L1, FMN2, GABBR1, GRIA1, GRIK2, GRIN2B +78 more Related via 90 shared genes including CDH15, CLIP1, CRADD.