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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 |
|---|---|---|---|
| 875 | CBS | cystathionine beta-synthase | |
| 1520 | CTSS | cathepsin S | |
| 1627 | DBN1 | drebrin 1 | |
| 1826 | DSCAM | DS cell adhesion molecule | |
| 1859 | DYRK1A | dual specificity tyrosine phosphorylation regulated kinase 1A | |
| 3329 | HSPD1 | heat shock protein family D (Hsp60) member 1 | |
| 3486 | IGFBP3 | insulin like growth factor binding protein 3 | |
| 4318 | MMP9 | matrix metallopeptidase 9 | |
| 4522 | MTHFD1 | methylenetetrahydrofolate dehydrogenase, cyclohydrolase and formyltetrahydrofolate synthetase 1 | |
| 5116 | PCNT | pericentrin |
| 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 |
