Term Name:	chromosome 16p12.2-p11.2 deletion syndrome
Synonyms:	16p11.2-p12.2 microdeletion syndrome, 16p11.2p12.2 microdeletion syndrome
Definition:	A chromosomal deletion syndrome that has_material_basis_in a chromosome 16p12.2-p11.2 deletion and that is characterized by dysmorphic facial features, feeding difficulties, recurrent ear infections, developmental delay, and cognitive impairment.
Ontology:	Human Disease [DOID:0060400]   ( DOID:0060400 )