List of MeSH codes (C16)

Last updated

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   C16congenital, hereditary, and neonatal diseases and abnormalities

MeSH   C16.131abnormalities

MeSH   C16.131.042abnormalities, drug-induced

MeSH   C16.131.077abnormalities, multiple

MeSH   C16.131.080abnormalities, radiation-induced

MeSH   C16.131.240cardiovascular abnormalities

MeSH   C16.131.260chromosome disorders

MeSH   C16.131.300DiGeorge syndrome

MeSH   C16.131.314digestive system abnormalities

MeSH   C16.131.384eye abnormalities

MeSH   C16.131.482lymphatic abnormalities

MeSH   C16.131.581monsters

MeSH   C16.131.621musculoskeletal abnormalities

MeSH   C16.131.666nervous system malformations

MeSH   C16.131.740respiratory system abnormalities

MeSH   C16.131.810situs inversus

MeSH   C16.131.831skin abnormalities

MeSH   C16.131.850stomatognathic system abnormalities

MeSH   C16.131.894thyroid dysgenesis

MeSH   C16.131.939urogenital abnormalities

MeSH   C16.300fetal diseases

MeSH   C16.300.030chorioamnionitis

MeSH   C16.300.060erythroblastosis, fetal

MeSH   C16.300.080fetal alcohol syndrome

MeSH   C16.300.100fetal hypoxia

MeSH   C16.300.390fetal growth retardation

MeSH   C16.300.570fetal macrosomia

MeSH   C16.300.580meconium aspiration syndrome

MeSH   C16.320genetic diseases, inborn

MeSH   C16.320.033adrenal hyperplasia, congenital

MeSH   C16.320.070anemia, hemolytic, congenital

MeSH   C16.320.077anemia, hypoplastic, congenital

MeSH   C16.320.080ataxia telangiectasia

MeSH   C16.320.099blood coagulation disorders, inherited

MeSH   C16.320.129CADASIL

MeSH   C16.320.160cardiomyopathy, hypertrophic, familial

MeSH   C16.320.170cherubism

MeSH   C16.320.180chromosome disorders

MeSH   C16.320.190cystic fibrosis

MeSH   C16.320.240dwarfism

MeSH   C16.320.290eye diseases, hereditary

MeSH   C16.320.306familial Mediterranean fever

MeSH   C16.320.322genetic diseases, x-linked

MeSH   C16.320.338genetic diseases, y-linked

MeSH   C16.320.355Hajdu–Cheney syndrome

MeSH   C16.320.365hemoglobinopathies

MeSH   C16.320.400heredodegenerative disorders, nervous system

MeSH   C16.320.427hyperthyroxinemia, familial dysalbuminemic

MeSH   C16.320.455Jervell and Lange-Nielsen syndrome

MeSH   C16.320.467kallmann syndrome

MeSH   C16.320.480kartagener syndrome

MeSH   C16.320.540marfan syndrome

MeSH   C16.320.565metabolism, inborn errors

MeSH   C16.320.577muscular dystrophies

MeSH   C16.320.590myasthenic syndromes, congenital

MeSH   C16.320.600nail–patella syndrome

MeSH   C16.320.700neoplastic syndromes, hereditary

MeSH   C16.320.737osteogenesis imperfecta

MeSH   C16.320.775pain insensitivity, congenital

MeSH   C16.320.800Romano–Ward syndrome

MeSH   C16.320.850skin diseases, genetic

MeSH   C16.320.925Werner syndrome

MeSH   C16.614infant, newborn, diseases

MeSH   C16.614.042amniotic band syndrome

MeSH   C16.614.053anemia, neonatal

MeSH   C16.614.092asphyxia neonatorum

MeSH   C16.614.131birth injuries

MeSH   C16.614.213cystic fibrosis

MeSH   C16.614.258epilepsy, benign neonatal

MeSH   C16.614.304erythroblastosis, fetal

MeSH   C16.614.378hemorrhagic disease of newborn

MeSH   C16.614.390hernia, umbilical

MeSH   C16.614.414hydrocephalus

MeSH   C16.614.438hydrophthalmos

MeSH   C16.614.451hyperbilirubinemia, neonatal

MeSH   C16.614.465hyperostosis, cortical, congenital

MeSH   C16.614.492ichthyosis

MeSH   C16.614.521infant, premature, diseases

MeSH   C16.614.580meconium aspiration syndrome

MeSH   C16.614.595Möbius syndrome

MeSH   C16.614.610neonatal abstinence syndrome

MeSH   C16.614.643nystagmus, congenital

MeSH   C16.614.677ophthalmia neonatorum

MeSH   C16.614.694persistent fetal circulation syndrome

MeSH   C16.614.716persistent hyperinsulinemia hypoglycemia of infancy

MeSH   C16.614.760Rothmund–Thomson syndrome

MeSH   C16.614.810sclerema neonatorum

MeSH   C16.614.815severe combined immunodeficiency

MeSH   C16.614.868syphilis, congenital

MeSH   C16.614.890thanatophoric dysplasia

MeSH   C16.614.909toxoplasmosis, congenital

MeSH   C16.614.947Wolman disease


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