MONDO_0013238 (chromosome 17q23.1-q23.2 deletion syndrome) can be described as follows. 17q23.1q23.2 microdeletion syndrome is a recently described syndrome characterized by developmental delay, microcephaly, short stature, heart defects and limb abnormalities. Also known as: 17q23.1-q23.2 microdeletion syndrome, 17q23.1q23.2 microdeletion syndrome, Del(17)(q23.1q23.2), chromosome 17q23.1-q23.2 deletion syndrome, isolated cases, monosomy 17q23.1-q23.2, monosomy 17q23.1q23.2.