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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