| Metadata | |
|---|---|
| ID | DOID:0060393 |
| Name | chromosome 15q11.2 deletion syndrome |
| Definition | A chromosomal deletion syndrome that is characterized by intellectual disability, dysmorphic facies, psychiatric illness and autism spectrum disorder, has_material_basis_in autosomal dominant inheritance of partial deletion of the long arm of chromosome 15. https://www.omim.org/entry/615656 |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Synonyms |
15q11.2 microdeletion syndrome [EXACT] |
| Parent Relationships | |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance |