DO_rare_slim chromosomal deletion syndrome chromosome 2p16.1-p15 deletion syndrome disease_ontology 2p15-p16.1 microdeletion syndrome ORDO:261349 MESH:C567289 2p15p16.1 microdeletion syndrome MIM:612513 DOID:0060415 GARD:13391 2015-09-28T17:32:44Z A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome 2p16.1-p15 region that is characterized by delayed psychomotor development, intellectual disability, and variable but distinctive dysmorphic features, including microcephaly, bitemporal narrowing, smooth and long philtrum, hypertelorism, downslanting palpebral fissures, broad nasal root, thin upper lip, and high palate. ICD10CM:Q93.5