chromosome 15q13.3 microdeletion syndrome (DOID:0060394)
Alliance: disease page
Synonyms: 15q13.3 microdeletion syndrome
Alt IDs: OMIM:612001, ICD10CM:Q93.5, MESH:C567439, ORDO:199318
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.