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MeSH descriptor
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Colic
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.
推出的年份:
副标题
blood
cerebrospinal fluid
chemically induced
classification
complications
congenital
diagnosis
diagnostic imaging
diet therapy
drug therapy
economics
embryology
enzymology
epidemiology
ethnology
etiology
genetics
history
immunology
metabolism
microbiology
mortality
nursing
parasitology
pathology
physiopathology
prevention and control
psychology
radiotherapy
rehabilitation
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urine
veterinary
virology
树号:
C16.614.166
MeSH 单一 ID:
D003085
进入的组:
Abdominal Cramps
Abdominal Cramp
Cramp, Abdominal
Cramps, Abdominal
Infantile Colic
Colic, Infantile
All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Infant, Newborn, Diseases [C16.614]
Amniotic Band Syndrome [C16.614.042]
Anemia, Neonatal [C16.614.053]
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Asphyxia Neonatorum [C16.614.092]
Birth Injuries [C16.614.131]
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Colic [C16.614.166]
Congenital Bone Marrow Failure Syndromes [C16.614.183]
Congenital Hyperinsulinism [C16.614.200]
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Cystic Fibrosis [C16.614.213]
Epilepsy, Benign Neonatal [C16.614.258]
Erythroblastosis, Fetal [C16.614.304]
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Hernia, Umbilical [C16.614.378]
Hydrophthalmos [C16.614.438]
Hyperbilirubinemia, Neonatal [C16.614.451]
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Hyperostosis, Cortical, Congenital [C16.614.465]
Ichthyosis [C16.614.492]
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Infant, Premature, Diseases [C16.614.521]
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Meconium Aspiration Syndrome [C16.614.580]
Mobius Syndrome [C16.614.595]
Neonatal Abstinence Syndrome [C16.614.610]
Neonatal Sepsis [C16.614.627]
Nystagmus, Congenital [C16.614.643]
Ophthalmia Neonatorum [C16.614.677]
Persistent Fetal Circulation Syndrome [C16.614.694]
Rothmund-Thomson Syndrome [C16.614.760]
Sclerema Neonatorum [C16.614.810]
Severe Combined Immunodeficiency [C16.614.815]
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Syphilis, Congenital [C16.614.868]
Thanatophoric Dysplasia [C16.614.890]
Thrombocytopenia, Neonatal Alloimmune [C16.614.899]
Toxoplasmosis, Congenital [C16.614.909]
Vitamin K Deficiency Bleeding [C16.614.940]
Wolman Disease [C16.614.947]
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