Monarch Disease Ontology entry MONDO_0016901 (partial deletion of the long arm of chromosome 2) can be described as follows. Chromosome 2q deletion is a chromosome abnormality that occurs when there is a missing copy of the genetic material located on the long arm (q) of chromosome 2. The severity of the condition and the signs and symptoms depend on the size and location of the deletion and which genes are involved. Features that often occur in people with chromosome 2q deletion include developmental delay, intellectual disability, behavioral problems, and distinctive facial features. Most cases are not inherited, but people can pass the deletion on to their children. Treatment is based on the signs and symptoms present in each person. Also known as: partial deletion of chromosome 2q, partial deletion of the long arm of chromosome type 2, partial monosomy of chromosome 2q, partial monosomy of the long arm of chromosome 2.