| Term Name: | cerebellofaciodental syndrome | 
|---|---|
| Synonyms: | cerebellar-facial-dental syndrome | 
| Definition: | A syndrome that is characterized by delayed development, intellectual disability, abnormal facial and dental findings, and cerebellar hypoplasia and that has_material_basis_in homozygous or compound heterozygous mutation in the BRF1 gene on chromosome 14q32. | 
| Ontology: | Human Disease [DOID:0080898] ( DOID:0080898 ) |