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MIRAGE
autistic disorder
Summary
- Synonym
-
- Kanner's syndrome
- autism
- autistic disorder of childhood onset
- childhood autism
- infantile autism
- Definition
- An autism spectrum disorder that is characterized by symptoms across all three symptom domains (communication, social, restricted repetitive interests and behaviors), delayed language development, and symptom onset prior to age 3 years.
- Super Class
- autism spectrum disorder
External Links
- Disease Ontology
- DOID:12849
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- ORDO
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 721 | C4B | complement C4B (Chido/Rodgers blood group) | |
| 1977 | EIF4E | eukaryotic translation initiation factor 4E | |
| 2020 | EN2 | engrailed homeobox 2 | |
| 2555 | GABRA2 | gamma-aminobutyric acid type A receptor subunit alpha2 | |
| 2557 | GABRA4 | gamma-aminobutyric acid type A receptor subunit alpha4 | |
| 2560 | GABRB1 | gamma-aminobutyric acid type A receptor subunit beta1 | |
| 2561 | GABRB2 | gamma-aminobutyric acid type A receptor subunit beta2 | |
| 2570 | GABRR2 | gamma-aminobutyric acid type A receptor subunit rho2 | |
| 2739 | GLO1 | glyoxalase I | |
| 2918 | GRM8 | glutamate metabotropic receptor 8 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P51608 | Methyl-CpG-binding protein 2 | |
| P78509 | Reelin | |
| Q15047 | Histone-lysine N-methyltransferase SETDB1 | |
| Q16620 | BDNF/NT-3 growth factors receptor | |
| Q8IVB4 | Sodium/hydrogen exchanger 9 | |
| Q8IZD2 | Inactive histone-lysine N-methyltransferase 2E | |
| Q8N0W4 | Neuroligin-4, X-linked | |
| Q8N2Q7 | Neuroligin-1 | |
| Q96NR3 | Patched domain-containing protein 1 | |
| Q99707 | Methionine synthase |
