Disease #00021
| Official abbreviation |
PCS |
| Name |
Premature chromatid separation trait |
| OMIM ID |
176430 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
0 |
| Phenotype entries for this disease |
0 |
| Associated with 1 gene |
BUB1B |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
|