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

Colic - Preferred

Concept UI	M0004742
Scope note	A clinical syndrome with intermittent abdominal pain characterized by sudden onset and cessation that is commonly seen in infants. It is usually associated with obstruction of the INTESTINES; of the CYSTIC DUCT; or of the URINARY TRACT.
Preferred term	Colic

Abdominal Cramps - Related but not broader or narrower

Concept UI	M0004741
Preferred term	Abdominal Cramps
Entry term(s)	Abdominal Cramp Cramp, Abdominal Cramps, Abdominal

Infantile Colic - Narrower

Concept UI	M0439077
Preferred term	Infantile Colic
Entry term(s)	Colic, Infantile