| Term Name: | Coffin-Siris syndrome 3 |
|---|---|
| Synonyms: | autosomal dominant mental retardation 15, CSS3, MRD15 |
| Definition: | A Coffin-Siris syndrome that has_material_basis_in an autosomal dominant mutation of the SMARCB1 gene on chromosome 22q11.23. |
| Ontology: | Human Disease [DOID:0070045] ( DOID:0070045 ) |