| Term Name: | Coffin-Siris syndrome 11 | 
|---|---|
| Synonyms: | CSS11 | 
| Definition: | A Coffin-Siris syndrome characterized by global developmental delay and impaired intellectual development associated with hypotonia, feeding difficulties, and variable dysmorphic features that has_material_basis_in heterozygous mutation in the SMARCD1 gene on chromosome 12q13.12. | 
| Ontology: | Human Disease [DOID:0112372] ( DOID:0112372 ) |