MONDO_0012864 (chromosome 2q32-q33 deletion syndrome) can be described as follows. 2q32q33 microdeletion syndrome is a recently described syndrome characterized by a variable phenotype involving moderate to severe intellectual deficit, significant speech delay, persistent feeding difficulties, growth retardation and dysmorphic features. Also known as: 2q32-q33 microdeletion syndrome, 2q32q33 microdeletion syndrome, Del(2)(q32), Del(2)(q32q33), glass syndrome, monosomy 2q32, monosomy 2q32-q33, monosomy 2q32q33.