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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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
External Links
- Disease Ontology
- DOID:0060307
- Mondo Disease Ontology
- ORDO
- OMIM
- GARD
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 23036 | ZNF292 | zinc finger protein 292 | |
| 23524 | SRRM2 | serine/arginine repetitive matrix 2 | |
| 26053 | AUTS2 | activator of transcription and developmental regulator AUTS2 | |
| 29072 | SETD2 | SET domain containing 2, histone lysine methyltransferase | |
| 55777 | MBD5 | methyl-CpG binding domain protein 5 | |
| 57609 | DIP2B | disco interacting protein 2 homolog B | |
| 64864 | RFX7 | regulatory factor X7 | |
| 81562 | LMAN2L | lectin, mannose binding 2 like |
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 11773 | Ap2m1 | adaptor-related protein complex 2, mu 1 subunit | |
| 12325 | Camk2g | calcium/calmodulin-dependent protein kinase II gamma | |
| 13385 | Dlg4 | discs large MAGUK scaffold protein 4 | |
| 14799 | Gria1 | glutamate receptor, ionotropic, AMPA1 (alpha 1) | |
| 15381 | Hnrnpc | heterogeneous nuclear ribonucleoprotein C | |
| 30046 | Zfp292 | zinc finger protein 292 | |
| 67972 | Atp2b1 | ATPase, Ca++ transporting, plasma membrane 1 | |
| 75410 | Kmt2b | lysine (K)-specific methyltransferase 2B | |
| 75956 | Srrm2 | serine/arginine repetitive matrix 2 | |
| 214895 | Lman2l | lectin, mannose-binding 2-like |
