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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 |
|---|---|---|---|
| 3123 | HLA-DRB1 | major histocompatibility complex, class II, DR beta 1 | |
| 3265 | HRAS | HRas proto-oncogene, GTPase | |
| 3329 | HSPD1 | heat shock protein family D (Hsp60) member 1 | |
| 3786 | KCNQ3 | potassium voltage-gated channel subfamily Q member 3 | |
| 3912 | LAMB1 | laminin subunit beta 1 | |
| 4204 | MECP2 | methyl-CpG binding protein 2 | |
| 4233 | MET | MET proto-oncogene, receptor tyrosine kinase | |
| 4548 | MTR | 5-methyltetrahydrofolate-homocysteine methyltransferase | |
| 4763 | NF1 | neurofibromin 1 | |
| 4915 | NTRK2 | neurotrophic receptor tyrosine kinase 2 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9H3R0 | Lysine-specific demethylase 4C | |
| Q9NZ94 | Neuroligin-3 | |
| Q9UHC6 | Contactin-associated protein-like 2 | |
| Q9UPX8 | SH3 and multiple ankyrin repeat domains protein 2 |
