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List of MeSH codes (C16)

From Wikipedia, the free encyclopedia

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

MeSH C16.131abnormalities

MeSH C16.131.042 – abnormalities, drug-induced

MeSH C16.131.077 – abnormalities, multiple

MeSH C16.131.080 – abnormalities, radiation-induced

MeSH C16.131.240cardiovascular abnormalities

MeSH C16.131.260chromosome disorders

MeSH C16.131.300DiGeorge syndrome

MeSH C16.131.314 – digestive system abnormalities

MeSH C16.131.384 – eye abnormalities

MeSH C16.131.482 – lymphatic abnormalities

MeSH C16.131.581monsters

MeSH C16.131.621musculoskeletal abnormalities

MeSH C16.131.666 – nervous system malformations

MeSH C16.131.740 – respiratory system abnormalities

MeSH C16.131.810situs inversus

MeSH C16.131.831skin abnormalities

MeSH C16.131.850 – stomatognathic system abnormalities

MeSH C16.131.894thyroid dysgenesis

MeSH C16.131.939 – urogenital abnormalities

MeSH C16.300 – fetal 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 C16.320.070 – anemia, hemolytic, congenital

MeSH C16.320.077anemia, hypoplastic, congenital

MeSH C16.320.080ataxia telangiectasia

MeSH C16.320.099 – blood coagulation disorders, inherited

MeSH C16.320.129CADASIL

MeSH C16.320.160 – cardiomyopathy, hypertrophic, familial

MeSH C16.320.170cherubism

MeSH C16.320.180chromosome disorders

MeSH C16.320.190cystic fibrosis

MeSH C16.320.240dwarfism

MeSH C16.320.290 – eye diseases, hereditary

MeSH C16.320.306familial Mediterranean fever

MeSH C16.320.322 – genetic diseases, x-linked

MeSH C16.320.338 – genetic 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 C16.320.590 – myasthenic syndromes, congenital

MeSH C16.320.600nail–patella syndrome

MeSH C16.320.700 – neoplastic 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 C16.614 – infant, newborn, diseases

MeSH C16.614.042amniotic band syndrome

MeSH C16.614.053 – anemia, 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 C16.614.451 – hyperbilirubinemia, 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).

This page was last edited on 12 April 2022, at 05:23
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