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
|
|