Congenital anomalies may affect a significant proportion of newly delivered babies and lead to a remarkable morbidity and mortality rate, so it is regarded as the leading cause of prenatal death and postnatal disability in many countries. Congenital anomalies, also known as congenital disabilities, affect the structure or function of many organs, which may result from a flaw or abnormality during the development phase. There is a variable prevalence of congenital anomalies in worldwide countries. In about 50% of congenital anomalies, the etiology is unknown, but in general, nearly (30-40%) of congenital malformation is genetic and environmental predisposition may account for about (5 to 10%). Prenatal and maternal history is essential to search for risk factors. When expecting congenital malformation, the accurate diagnosis has been done prenatally through either non-invasive techniques or invasive techniques. Because the rehabilitation and treatment of these babies with congenital malformations is complex and expensive, and the prevention of these conditions is only possible in 60% of cases, it is critical to determine causative and risk factors and avoid them early. To standardize records and include more detail about the prevalence of common and unusual abnormalities, epidemiological information obtained through the creation of populationbased registries is critical. As a result, knowing the pattern and prevalence of congenital anomalies can help determine baseline rates, monitor changes over time, recognize clues to the etiology of conditions, and prepare and assess antenatal screening for congenital anomalies, especially in the high communities. This research aims to determine what kinds of congenital abnormalities there are in live newborns and how common they are. The study was done in Karbala’s “neonatal intensive care unit” hospital for children in Karbala, Iraq. The study was conducted over a 24 month period from March 1, 2019, to February 30, 2021. Overt manifestation of deformities was evaluated systematically through history, clinical examination and other features of congenital anomalies were based on further necessary investigation such as radiography, ultrasonography and echocardiography, etc. Two hundred and ten newborns with congenital abnormalities were included in this study, males 128 (60.95%) and females 82 (39.05%). According to the International Classification of Disease (ICD) 10, the pattern of congenital anomalies was classified with systemic involvement [central nervous system (CNS), genitor- urinary system (GUS), cardiovascular system (CVS), gastro-intestinal (GIT), musculoskeletal (MS) and skin]. In the present study, the type of congenital anomalies which are more predominant is related to the cardiovascular system (CVS) 57 (27.14%). CVS anomalies included simple and cyanotic 44 (77.2%) and complex and cyanotic 13 (22.8%) congenital heart disease. The gastrointestinal system anomalies were 51 (24.28%), in which the duodenal atresia 13 (25.49%) and the cleft lip and palate 8 (15.68%). At the same time, the central nervous system anomalies are the third typical pattern of anomalies which account for about 32 (15.23%); meningomyelocele 15 (46.87%) and hydrocephalus 7 (21.87%). Male babies are affected by congenital anomalies more than females, and the full-term neonate has had a prevailing rate of affection. The cardiovascular system is mainly affected by congenital anomalies with predominant prevalence in males and full-term babies more than preterm. [ABSTRACT FROM AUTHOR]