List of MeSH codes (C16)

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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).

Contents

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

MeSH C16.131 – abnormalities

MeSH C16.131.042 – abnormalities, drug-induced

MeSH C16.131.077 – abnormalities, multiple

MeSH C16.131.080 – abnormalities, radiation-induced

MeSH C16.131.240 – cardiovascular abnormalities

MeSH C16.131.260 – chromosome disorders

MeSH C16.131.300 – DiGeorge syndrome

MeSH C16.131.314 – digestive system abnormalities

MeSH C16.131.384 – eye abnormalities

MeSH C16.131.482 – lymphatic abnormalities

MeSH C16.131.581 – monsters

MeSH C16.131.621 – musculoskeletal abnormalities

MeSH C16.131.666 – nervous system malformations

MeSH C16.131.740 – respiratory system abnormalities

MeSH C16.131.810 – situs inversus

MeSH C16.131.831 – skin abnormalities

MeSH C16.131.850 – stomatognathic system abnormalities

MeSH C16.131.894 – thyroid dysgenesis

MeSH C16.131.939 – urogenital abnormalities

MeSH C16.300 – fetal diseases

MeSH C16.300.030 – chorioamnionitis

MeSH C16.300.060 – erythroblastosis, fetal

MeSH C16.300.080 – fetal alcohol syndrome

MeSH C16.300.100 – fetal hypoxia

MeSH C16.300.390 – fetal growth retardation

MeSH C16.300.570 – fetal macrosomia

MeSH C16.300.580 – meconium aspiration syndrome

MeSH C16.320 – genetic diseases, inborn

MeSH C16.320.033 – adrenal hyperplasia, congenital

MeSH C16.320.070 – anemia, hemolytic, congenital

MeSH C16.320.077 – anemia, hypoplastic, congenital

MeSH C16.320.080 – ataxia telangiectasia

MeSH C16.320.099 – blood coagulation disorders, inherited

MeSH C16.320.129 – CADASIL

MeSH C16.320.160 – cardiomyopathy, hypertrophic, familial

MeSH C16.320.170 – cherubism

MeSH C16.320.180 – chromosome disorders

MeSH C16.320.190 – cystic fibrosis

MeSH C16.320.240 – dwarfism

MeSH C16.320.290 – eye diseases, hereditary

MeSH C16.320.306 – familial Mediterranean fever

MeSH C16.320.322 – genetic diseases, x-linked

MeSH C16.320.338 – genetic diseases, y-linked

MeSH C16.320.355 – Hajdu–Cheney syndrome

MeSH C16.320.365 – hemoglobinopathies

MeSH C16.320.400 – heredodegenerative disorders, nervous system

MeSH C16.320.427 – hyperthyroxinemia, familial dysalbuminemic

MeSH C16.320.455 – Jervell and Lange-Nielsen syndrome

MeSH C16.320.467 – kallmann syndrome

MeSH C16.320.480 – kartagener syndrome

MeSH C16.320.540 – marfan syndrome

MeSH C16.320.565 – metabolism, inborn errors

MeSH C16.320.577 – muscular dystrophies

MeSH C16.320.590 – myasthenic syndromes, congenital

MeSH C16.320.600 – nail–patella syndrome

MeSH C16.320.700 – neoplastic syndromes, hereditary

MeSH C16.320.737 – osteogenesis imperfecta

MeSH C16.320.775 – pain insensitivity, congenital

MeSH C16.320.800 – Romano–Ward syndrome

MeSH C16.320.850 – skin diseases, genetic

MeSH C16.320.925 – Werner syndrome

MeSH C16.614 – infant, newborn, diseases

MeSH C16.614.042 – amniotic band syndrome

MeSH C16.614.053 – anemia, neonatal

MeSH C16.614.092 – asphyxia neonatorum

MeSH C16.614.131 – birth injuries

MeSH C16.614.213 – cystic fibrosis

MeSH C16.614.258 – epilepsy, benign neonatal

MeSH C16.614.304 – erythroblastosis, fetal

MeSH C16.614.378 – hemorrhagic disease of newborn

MeSH C16.614.390 – hernia, umbilical

MeSH C16.614.414 – hydrocephalus

MeSH C16.614.438 – hydrophthalmos

MeSH C16.614.451 – hyperbilirubinemia, neonatal

MeSH C16.614.465 – hyperostosis, cortical, congenital

MeSH C16.614.492 – ichthyosis

MeSH C16.614.521 – infant, premature, diseases

MeSH C16.614.580 – meconium aspiration syndrome

MeSH C16.614.595 – Möbius syndrome

MeSH C16.614.610 – neonatal abstinence syndrome

MeSH C16.614.643 – nystagmus, congenital

MeSH C16.614.677 – ophthalmia neonatorum

MeSH C16.614.694 – persistent fetal circulation syndrome

MeSH C16.614.716 – persistent hyperinsulinemia hypoglycemia of infancy

MeSH C16.614.760 – Rothmund–Thomson syndrome

MeSH C16.614.810 – sclerema neonatorum

MeSH C16.614.815 – severe combined immunodeficiency

MeSH C16.614.868 – syphilis, congenital

MeSH C16.614.890 – thanatophoric dysplasia

MeSH C16.614.909 – toxoplasmosis, congenital

MeSH C16.614.947 – Wolman disease

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

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