DISEASES Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] Congenital, Hereditary, and Neonatal Diseases and Abnormalities Infant, Newborn, Diseases [C16.614] Infant, Newborn, Diseases Amniotic Band Syndrome [C16.614.042] Amniotic Band Syndrome Anemia, Neonatal [C16.614.053] Anemia, Neonatal Asphyxia Neonatorum [C16.614.092] Asphyxia Neonatorum Birth Injuries [C16.614.131] Birth Injuries Colic [C16.614.166] Colic Congenital Bone Marrow Failure Syndromes [C16.614.183] Congenital Bone Marrow Failure Syndromes Congenital Hyperinsulinism [C16.614.200] Congenital Hyperinsulinism Cystic Fibrosis [C16.614.213] Cystic Fibrosis Epilepsy, Benign Neonatal [C16.614.258] Epilepsy, Benign Neonatal Erythroblastosis, Fetal [C16.614.304] Erythroblastosis, Fetal Hernia, Umbilical [C16.614.378] Hernia, Umbilical Hydrophthalmos [C16.614.438] Hydrophthalmos Hyperbilirubinemia, Neonatal [C16.614.451] Hyperbilirubinemia, Neonatal Hyperostosis, Cortical, Congenital [C16.614.465] Hyperostosis, Cortical, Congenital Ichthyosis [C16.614.492] Ichthyosis Infant, Premature, Diseases [C16.614.521] Infant, Premature, Diseases Meconium Aspiration Syndrome [C16.614.580] Meconium Aspiration Syndrome Mobius Syndrome [C16.614.595] Mobius Syndrome Neonatal Abstinence Syndrome [C16.614.610] Neonatal Abstinence Syndrome Neonatal Sepsis [C16.614.627] Neonatal Sepsis Nystagmus, Congenital [C16.614.643] Nystagmus, Congenital Ophthalmia Neonatorum [C16.614.677] Ophthalmia Neonatorum Persistent Fetal Circulation Syndrome [C16.614.694] Persistent Fetal Circulation Syndrome Rothmund-Thomson Syndrome [C16.614.760] Rothmund-Thomson Syndrome Sclerema Neonatorum [C16.614.810] Sclerema Neonatorum Severe Combined Immunodeficiency [C16.614.815] Severe Combined Immunodeficiency Syphilis, Congenital [C16.614.868] Syphilis, Congenital Thanatophoric Dysplasia [C16.614.890] Thanatophoric Dysplasia Thrombocytopenia, Neonatal Alloimmune [C16.614.899] Thrombocytopenia, Neonatal Alloimmune Toxoplasmosis, Congenital [C16.614.909] Toxoplasmosis, Congenital Vitamin K Deficiency Bleeding [C16.614.940] Vitamin K Deficiency Bleeding Wolman Disease [C16.614.947] Wolman Disease DISEASES Pathological Conditions, Signs and Symptoms [C23] Pathological Conditions, Signs and Symptoms Pathological Conditions, Anatomical [C23.300] Pathological Conditions, Anatomical Hernia [C23.300.707] Hernia Hernia, Abdominal [C23.300.707.374] Hernia, Abdominal Hernia, Ventral [C23.300.707.374.937] Hernia, Ventral Hernia, Umbilical [C23.300.707.374.937.500] Hernia, Umbilical

Hernia, Umbilical - Preferred

Concept UI	M0010269
Scope note	A HERNIA due to an imperfect closure or weakness of the umbilical ring. It appears as a skin-covered protrusion at the UMBILICUS during crying, coughing, or straining. The hernia generally consists of OMENTUM or SMALL INTESTINE. The vast majority of umbilical hernias are congenital but can be acquired due to severe abdominal distention.
Preferred term	Hernia, Umbilical
Entry term(s)	Exomphalos Hernias, Umbilical Umbilical Hernia Umbilical Hernias

Omphalocele - Narrower

Concept UI	M0010270
Scope note	A congenital defect with major fissure in the ABDOMINAL WALL at the UMBILICUS resulting in the extrusion of VISCERA through the UMBILICUS. Unlike GASTROSCHISIS, omphalocele is covered with PERITONEUM but without overlying SKIN.
Preferred term	Omphalocele
Entry term(s)	Omphaloceles