Wikipedia

List of MeSH codes (C16)

The following is a partial list of the "C" codes for Medical Subject Headings (MeSH), as defined by the United States National Library of Medicine (NLM).

This list continues the information at List of MeSH codes (C15). Codes following these are found at List of MeSH codes (C17). For other MeSH codes, see List of MeSH codes.

The source for this content is the set of 2006 MeSH Trees from the NLM.

MeSH C16 – congenital, hereditary, and neonatal diseases and abnormalities

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MeSH C16.131 – abnormalities

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MeSH C16.131.042 – abnormalities, drug-induced

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MeSH C16.131.077 – abnormalities, multiple

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MeSH C16.131.080 – abnormalities, radiation-induced

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MeSH C16.131.240 – cardiovascular abnormalities

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MeSH C16.131.260 – chromosome disorders

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MeSH C16.131.300 – DiGeorge syndrome

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MeSH C16.131.314 – digestive system abnormalities

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MeSH C16.131.384 – eye abnormalities

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MeSH C16.131.482 – lymphatic abnormalities

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MeSH C16.131.581 – monsters

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MeSH C16.131.621 – musculoskeletal abnormalities

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MeSH C16.131.666 – nervous system malformations

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MeSH C16.131.740 – respiratory system abnormalities

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MeSH C16.131.810 – situs inversus

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MeSH C16.131.831 – skin abnormalities

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MeSH C16.131.850 – stomatognathic system abnormalities

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MeSH C16.131.894 – thyroid dysgenesis

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MeSH C16.131.939 – urogenital abnormalities

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MeSH C16.300 – fetal diseases

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MeSH C16.300.030 – chorioamnionitis

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MeSH C16.300.060 – erythroblastosis, fetal

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MeSH C16.300.080 – fetal alcohol syndrome

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MeSH C16.300.100 – fetal hypoxia

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MeSH C16.300.390 – fetal growth retardation

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MeSH C16.300.570 – fetal macrosomia

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MeSH C16.300.580 – meconium aspiration syndrome

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MeSH C16.320 – genetic diseases, inborn

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MeSH C16.320.033 – adrenal hyperplasia, congenital

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MeSH C16.320.070 – anemia, hemolytic, congenital

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MeSH C16.320.077 – anemia, hypoplastic, congenital

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MeSH C16.320.080 – ataxia telangiectasia

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MeSH C16.320.099 – blood coagulation disorders, inherited

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MeSH C16.320.129 – CADASIL

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MeSH C16.320.160 – cardiomyopathy, hypertrophic, familial

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MeSH C16.320.170 – cherubism

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MeSH C16.320.180 – chromosome disorders

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MeSH C16.320.190 – cystic fibrosis

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MeSH C16.320.240 – dwarfism

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MeSH C16.320.290 – eye diseases, hereditary

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MeSH C16.320.306 – familial Mediterranean fever

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MeSH C16.320.322 – genetic diseases, x-linked

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MeSH C16.320.338 – genetic diseases, y-linked

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MeSH C16.320.355 – Hajdu–Cheney syndrome

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MeSH C16.320.365 – hemoglobinopathies

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MeSH C16.320.400 – heredodegenerative disorders, nervous system

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MeSH C16.320.427 – hyperthyroxinemia, familial dysalbuminemic

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MeSH C16.320.455 – Jervell and Lange-Nielsen syndrome

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MeSH C16.320.467 – kallmann syndrome

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MeSH C16.320.480 – kartagener syndrome

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MeSH C16.320.540 – marfan syndrome

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MeSH C16.320.565 – metabolism, inborn errors

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MeSH C16.320.577 – muscular dystrophies

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MeSH C16.320.590 – myasthenic syndromes, congenital

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MeSH C16.320.600 – nail–patella syndrome

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MeSH C16.320.700 – neoplastic syndromes, hereditary

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MeSH C16.320.737 – osteogenesis imperfecta

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MeSH C16.320.775 – pain insensitivity, congenital

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MeSH C16.320.800 – Romano–Ward syndrome

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MeSH C16.320.850 – skin diseases, genetic

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MeSH C16.320.925 – Werner syndrome

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MeSH C16.614 – infant, newborn, diseases

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MeSH C16.614.042 – amniotic band syndrome

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MeSH C16.614.053 – anemia, neonatal

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MeSH C16.614.092 – asphyxia neonatorum

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MeSH C16.614.131 – birth injuries

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MeSH C16.614.213 – cystic fibrosis

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MeSH C16.614.258 – epilepsy, benign neonatal

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MeSH C16.614.304 – erythroblastosis, fetal

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MeSH C16.614.378 – hemorrhagic disease of newborn

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MeSH C16.614.390 – hernia, umbilical

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MeSH C16.614.414 – hydrocephalus

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MeSH C16.614.438 – hydrophthalmos

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MeSH C16.614.451 – hyperbilirubinemia, neonatal

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MeSH C16.614.465 – hyperostosis, cortical, congenital

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MeSH C16.614.492 – ichthyosis

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MeSH C16.614.521 – infant, premature, diseases

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MeSH C16.614.580 – meconium aspiration syndrome

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MeSH C16.614.595 – Möbius syndrome

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MeSH C16.614.610 – neonatal abstinence syndrome

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MeSH C16.614.643 – nystagmus, congenital

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MeSH C16.614.677 – ophthalmia neonatorum

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MeSH C16.614.694 – persistent fetal circulation syndrome

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MeSH C16.614.716 – persistent hyperinsulinemia hypoglycemia of infancy

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MeSH C16.614.760 – Rothmund–Thomson syndrome

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MeSH C16.614.810 – sclerema neonatorum

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MeSH C16.614.815 – severe combined immunodeficiency

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MeSH C16.614.868 – syphilis, congenital

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MeSH C16.614.890 – thanatophoric dysplasia

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MeSH C16.614.909 – toxoplasmosis, congenital

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MeSH C16.614.947 – Wolman disease

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The list continues at List of MeSH codes (C17).

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