A condition in which some or all of the cells of the body contain extra genetic material from chromosome 18. Clinical features of this condition may include the following: spina bifida, hearing loss, cleft lip, cleft palate, undescended testes, rocker bottom feet, micrognathia, low set ears, cardiac anomalies (ventricular septal defect, atrial septal defect, patent ductus arteriosus, tetralogy of Fallot), intellectual disability, holoprosencephaly, pituitary dysplasia, seizures, autoimmune disorders, hip dysplasia, and/or congenital cataracts. The disease is Monarch Disease Ontology identifier MONDO_0011147 (chromosome 18q deletion syndrome). Also known as: 18Q syndrome, 18q deletion syndrome, 18q-syndrome, Chromosome 18q- Syndrome, deletion 18q, deletion 18q syndrome, monosomy 18q, monosomy type 18q.