A rare multisystem genetic disorder characterized by lentigines, hypertrophic cardiomyopathy, short stature, pectus deformity, and dysmorphic facial features. The disease is MONDO_0007893 (Noonan syndrome with multiple lentigines). Also known as: Capute-Rimoin-Konigsmark-Esterly-Richardson syndrome, Cardiomyopathic lentiginosis, Gorlin syndrome II, LEOPARD syndrome, familial multiple lentigines syndrome, generalised lentiginosis, generalized lentiginosis, lentigines, electrocardiographic conduction defects, 0cular hypertelorism, pulmonary stenosis, abnormalities of the genitals, retarded Growth, deafness.