| Term Name: | developmental delay, hypotonia, and impaired language |
|---|---|
| Synonyms: | DEDHIL |
| Definition: | An autosomal dominant intellectual developmental disorder characterized by variably impaired intellectual development usually with hypotonia, mild motor delay, and language difficulties that has_material_basis_in heterozygous mutation in the FBXW7 gene on chromosome 4q31. |
| Ontology: | Human Disease [DOID:0070420] ( DOID:0070420 ) |