List of MeSH codes (C16)

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The following is a list of the "C" codes for MeSH. It is a product of the United States National Library of Medicine.

Source for content is here. (File "2006 MeSH Trees".)


MeSH C16 --- congenital, hereditary, and neonatal diseases and abnormalities[edit]

MeSH C16.131 --- abnormalities[edit]

MeSH C16.131.042 --- abnormalities, drug-induced[edit]

MeSH C16.131.077 --- abnormalities, multiple[edit]

MeSH C16.131.080 --- abnormalities, radiation-induced[edit]

MeSH C16.131.240 --- cardiovascular abnormalities[edit]

MeSH C16.131.260 --- chromosome disorders[edit]

MeSH C16.131.300 --- digeorge syndrome[edit]

MeSH C16.131.314 --- digestive system abnormalities[edit]

MeSH C16.131.384 --- eye abnormalities[edit]

MeSH C16.131.482 --- lymphatic abnormalities[edit]

MeSH C16.131.581 --- monsters[edit]

MeSH C16.131.621 --- musculoskeletal abnormalities[edit]

MeSH C16.131.666 --- nervous system malformations[edit]

MeSH C16.131.740 --- respiratory system abnormalities[edit]

MeSH C16.131.810 --- situs inversus[edit]

MeSH C16.131.831 --- skin abnormalities[edit]

MeSH C16.131.850 --- stomatognathic system abnormalities[edit]

MeSH C16.131.894 --- thyroid dysgenesis[edit]

MeSH C16.131.939 --- urogenital abnormalities[edit]

MeSH C16.300 --- fetal diseases[edit]

MeSH C16.300.030 --- chorioamnionitis[edit]

MeSH C16.300.060 --- erythroblastosis, fetal[edit]

MeSH C16.300.080 --- fetal alcohol syndrome[edit]

MeSH C16.300.100 --- fetal hypoxia[edit]

MeSH C16.300.390 --- fetal growth retardation[edit]

MeSH C16.300.570 --- fetal macrosomia[edit]

MeSH C16.300.580 --- meconium aspiration syndrome[edit]

MeSH C16.320 --- genetic diseases, inborn[edit]

MeSH C16.320.033 --- adrenal hyperplasia, congenital[edit]

MeSH C16.320.070 --- anemia, hemolytic, congenital[edit]

MeSH C16.320.077 --- anemia, hypoplastic, congenital[edit]

MeSH C16.320.080 --- ataxia telangiectasia[edit]

MeSH C16.320.099 --- blood coagulation disorders, inherited[edit]

MeSH C16.320.129 --- cadasil[edit]

MeSH C16.320.160 --- cardiomyopathy, hypertrophic, familial[edit]

MeSH C16.320.170 --- cherubism[edit]

MeSH C16.320.180 --- chromosome disorders[edit]

MeSH C16.320.190 --- cystic fibrosis[edit]

MeSH C16.320.240 --- dwarfism[edit]

MeSH C16.320.290 --- eye diseases, hereditary[edit]

MeSH C16.320.306 --- familial mediterranean fever[edit]

MeSH C16.320.322 --- genetic diseases, x-linked[edit]

MeSH C16.320.338 --- genetic diseases, y-linked[edit]

MeSH C16.320.355 --- hajdu-cheney syndrome[edit]

MeSH C16.320.365 --- hemoglobinopathies[edit]

MeSH C16.320.400 --- heredodegenerative disorders, nervous system[edit]

MeSH C16.320.427 --- hyperthyroxinemia, familial dysalbuminemic[edit]

MeSH C16.320.455 --- jervell-lange nielsen syndrome[edit]

MeSH C16.320.467 --- kallmann syndrome[edit]

MeSH C16.320.480 --- kartagener syndrome[edit]

MeSH C16.320.540 --- marfan syndrome[edit]

MeSH C16.320.565 --- metabolism, inborn errors[edit]

MeSH C16.320.577 --- muscular dystrophies[edit]

MeSH C16.320.590 --- myasthenic syndromes, congenital[edit]

MeSH C16.320.600 --- nail-patella syndrome[edit]

MeSH C16.320.700 --- neoplastic syndromes, hereditary[edit]

MeSH C16.320.737 --- osteogenesis imperfecta[edit]

MeSH C16.320.775 --- pain insensitivity, congenital[edit]

MeSH C16.320.800 --- romano-ward syndrome[edit]

MeSH C16.320.850 --- skin diseases, genetic[edit]

MeSH C16.320.925 --- werner syndrome[edit]

MeSH C16.614 --- infant, newborn, diseases[edit]

MeSH C16.614.042 --- amniotic band syndrome[edit]

MeSH C16.614.053 --- anemia, neonatal[edit]

MeSH C16.614.092 --- asphyxia neonatorum[edit]

MeSH C16.614.131 --- birth injuries[edit]

MeSH C16.614.213 --- cystic fibrosis[edit]

MeSH C16.614.258 --- epilepsy, benign neonatal[edit]

MeSH C16.614.304 --- erythroblastosis, fetal[edit]

MeSH C16.614.378 --- hemorrhagic disease of newborn[edit]

MeSH C16.614.390 --- hernia, umbilical[edit]

MeSH C16.614.414 --- hydrocephalus[edit]

MeSH C16.614.438 --- hydrophthalmos[edit]

MeSH C16.614.451 --- hyperbilirubinemia, neonatal[edit]

MeSH C16.614.465 --- hyperostosis, cortical, congenital[edit]

MeSH C16.614.492 --- ichthyosis[edit]

MeSH C16.614.521 --- infant, premature, diseases[edit]

MeSH C16.614.580 --- meconium aspiration syndrome[edit]

MeSH C16.614.595 --- mobius syndrome[edit]

MeSH C16.614.610 --- neonatal abstinence syndrome[edit]

MeSH C16.614.643 --- nystagmus, congenital[edit]

MeSH C16.614.677 --- ophthalmia neonatorum[edit]

MeSH C16.614.694 --- persistent fetal circulation syndrome[edit]

MeSH C16.614.716 --- persistent hyperinsulinemia hypoglycemia of infancy[edit]

MeSH C16.614.760 --- rothmund-thomson syndrome[edit]

MeSH C16.614.810 --- sclerema neonatorum[edit]

MeSH C16.614.815 --- severe combined immunodeficiency[edit]

MeSH C16.614.868 --- syphilis, congenital[edit]

MeSH C16.614.890 --- thanatophoric dysplasia[edit]

MeSH C16.614.909 --- toxoplasmosis, congenital[edit]

MeSH C16.614.947 --- wolman disease[edit]