| Term Name: | chromosome 15q13.3 microdeletion syndrome |
|---|---|
| Synonyms: | 15q13.3 microdeletion syndrome |
| Definition: | A chromosomal deletion syndrome that is characterized by intellectual dsability, developmental delay, autism spectrum disorder and seizure, has_material_basis_in autosomal dominant inheritance of partial deletion of the long arm of chromosome 15. |
| Ontology: | Human Disease [DOID:0060394] ( DOID:0060394 ) |