Disease #00144
| Official abbreviation |
CSS3 |
| Name |
Coffin-Siris syndrome 3 |
| OMIM ID |
614608 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
0 |
| Phenotype entries for this disease |
0 |
| Associated with 1 gene |
SMARCB1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
|