"ORDO:261222"^^ . "OMIM:613444"^^ . "2015-09-28T16:35:34Z"^^ . "A chromosomal deletion syndrome that is characterized by developmental delay, mild intellectual disability and autism spectrum disorder and that has_material_basis_in a partial deletion of the short arm of chromosome 16, specifically a deletion of a 220-kb region on chromosome 16p11.2 encompassing approximately 9 genes, including the SH2B1 gene."^^ . . "chromosome 16p11.2 deletion syndrome"^^ . "distal 16p11.2 microdeletion syndrome"@en . . "ICD10CM:Q93.5"^^ . "disease_ontology"^^ . . "elvira"^^ . "DOID:0060398"^^ . .