Disease #00005 (CS (Cockayne Syndrome), OMIM:216400)
| Official abbreviation |
CS |
| Name |
Cockayne Syndrome |
| OMIM ID |
216400 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
123 |
| Phenotype entries for this disease |
- |
| Associated with 3 genes |
ERCC5, ERCC6, ERCC8 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
Individuals
|
|