| Metadata | |
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| ID | DOID:0112367 | 
| Name | Coffin-Siris syndrome 8 | 
| Definition | A Coffin-Siris syndrome characterized by variable degrees of impaired intellectual development including speech impairment, hypotonia, feeding difficulties, and behavioral abnormalities and variable occurence of other dysmophic features that has_material_basis_in heterozygous mutation in the SMARCC2 gene on chromosome 12q13.  https://pubmed.ncbi.nlm.nih.gov/30580808/  | 
			    
                        
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	                             has material basis in some autosomal dominant inheritance  |