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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Down syndrome
Summary
- Synonym
-
- Complete trisomy 21 syndrome
- Down's syndrome
- Down's syndrome - trisomy 21
- Downs syndrome
- G Trisomy
- trisomy 21 syndrome
- Definition
- A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability.
- Super Class
- chromosomal duplication syndrome
External Links
- Disease Ontology
- DOID:14250
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- ORDO
- OMIM
- GARD
- MGI genotype (from TogoID)
- WikiPathways (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 13040 | Ctss | cathepsin S | |
| 13508 | Dscam | DS cell adhesion molecule | |
| 13549 | Dyrk1b | dual-specificity tyrosine phosphorylation regulated kinase 1b | |
| 15510 | Hspd1 | heat shock protein 1 (chaperonin) | |
| 16009 | Igfbp3 | insulin-like growth factor binding protein 3 | |
| 17395 | Mmp9 | matrix metallopeptidase 9 | |
| 17957 | Napb | N-ethylmaleimide sensitive fusion protein attachment protein beta | |
| 19699 | Reln | reelin | |
| 20614 | Snap25 | synaptosomal-associated protein 25 | |
| 20655 | Sod1 | superoxide dismutase 1, soluble |
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 24484 | Igfbp3 | insulin-like growth factor binding protein 3 | |
| 24718 | Reln | reelin | |
| 50654 | Ctss | cathepsin S | |
| 63868 | Hspd1 | heat shock protein family D (Hsp60) member 1 | |
| 81687 | Mmp9 | matrix metallopeptidase 9 | |
| 85238 | Synj1 | synaptojanin 1 | |
| 116510 | Timp1 | TIMP metallopeptidase inhibitor 1 | |
| 171119 | Dscam | DS cell adhesion molecule | |
| 309686 | Pofut2 | protein O-fucosyltransferase 2 |
