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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
stereotypic movement disorder
Summary
- Synonym
-
- Stereotyped repetitive movements
- Stereotypy habit disorder
- Definition
- A specific developmental disorder that is characterized by repeated, rhythmic, purposeless movements or activities such as head banging, nail biting, or body rocking.
- Super Class
- specific developmental disorder
External Links
- Disease Ontology
- DOID:2303
- Mondo Disease Ontology
- MeSH
- UMLS
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 8869 | ST3GAL5 | ST3 beta-galactoside alpha-2,3-sialyltransferase 5 | |
| 9524 | TECR | trans-2,3-enoyl-CoA reductase | |
| 11253 | MAN1B1 | mannosidase alpha class 1B member 1 | |
| 79143 | MBOAT7 | membrane bound O-acyltransferase domain containing 7 | |
| 80055 | PGAP1 | post-GPI attachment to proteins inositol deacylase 1 | |
| 81562 | LMAN2L | lectin, mannose binding 2 like | |
| 138050 | HGSNAT | heparan-alpha-glucosaminide N-acetyltransferase | |
| 148789 | B3GALNT2 | beta-1,3-N-acetylgalactosaminyltransferase 2 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q93063 | Exostosin-2 | |
| Q96N66 | Lysophospholipid acyltransferase 7 | |
| Q9H0V9 | VIP36-like protein | |
| Q9NZ01 | Very-long-chain enoyl-CoA reductase | |
| Q9UKM7 | Endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase | |
| Q9UNP4 | Lactosylceramide alpha-2,3-sialyltransferase |
