autosomal dominant intellectual developmental disorder

Summary
Synonym
  • autosomal dominant mental retardation
  • autosomal dominant non-syndromic mental retardation
Definition
A intellectual disability characterized by an autosomal dominant inheritance pattern.
Super Class
autosomal dominant disease intellectual disability
Disease Ontology
DOID:0060307
Mondo Disease Ontology
ORDO
OMIM
GARD
Related Genes
Displaying entries 1 - 10 of 18 in total
Gene ID Gene Symbol Description Source
818 CAMK2G calcium/calmodulin dependent protein kinase II gamma
1173 AP2M1 adaptor related protein complex 2 subunit mu 1
2890 GRIA1 glutamate ionotropic receptor AMPA type subunit 1
3183 HNRNPC heterogeneous nuclear ribonucleoprotein C
6418 SET SET nuclear proto-oncogene
6874 TAF4 TATA-box binding protein associated factor 4
7204 TRIO trio Rho guanine nucleotide exchange factor
9757 KMT2B lysine methyltransferase 2B
9969 MED13 mediator complex subunit 13
11011 TLK2 tousled like kinase 2
Displaying entries 11 - 13 of 13 in total
Gene ID Gene Symbol Description Source
223435 Trio triple functional domain (PTPRF interacting)
228980 Taf4 TATA-box binding protein associated factor 4
235626 Setd2 SET domain containing 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
50592 Gria1 glutamate ionotropic receptor AMPA type subunit 1
Displaying all 4 entries
Gene ID Gene Symbol Description Source
32547 tay tay bridge
38742 GluRIA Glutamate receptor IA
39765 Taf4 TBP-associated factor 4
41737 trx trithorax
Displaying all 3 entries
Gene ID Gene Symbol Description Source
175999 glr-2 Glutamate receptor 2
176204 glr-1 Glutamate receptor 1
3565539 dip-2 AMP-dependent synthetase/ligase domain-containing protein;DMAP1-binding domain-containing protein
Displaying all 3 entries
Gene ID Gene Symbol Description Source
851670 GIS1 histone demethylase GIS1
852053 SSN2 Ssn2p
854260 CMR2 Cmr2p

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Last updated: December 9, 2024