[{"@context":"http:\/\/schema.org\/","@type":"BlogPosting","@id":"https:\/\/wiki.edu.vn\/en\/list-of-mesh-codes-c18\/#BlogPosting","mainEntityOfPage":"https:\/\/wiki.edu.vn\/en\/list-of-mesh-codes-c18\/","headline":"List of MeSH codes (C18)","name":"List of MeSH codes (C18)","description":"before-content-x4 From Wikipedia, the free encyclopedia after-content-x4 This article needs to be updated. The reason given is: no files for","datePublished":"2019-09-19","dateModified":"2019-09-19","author":{"@type":"Person","@id":"https:\/\/wiki.edu.vn\/en\/author\/lordneo\/#Person","name":"lordneo","url":"https:\/\/wiki.edu.vn\/en\/author\/lordneo\/","image":{"@type":"ImageObject","@id":"https:\/\/secure.gravatar.com\/avatar\/cd810e53c1408c38cc766bc14e7ce26a?s=96&d=mm&r=g","url":"https:\/\/secure.gravatar.com\/avatar\/cd810e53c1408c38cc766bc14e7ce26a?s=96&d=mm&r=g","height":96,"width":96}},"publisher":{"@type":"Organization","name":"Enzyklop\u00e4die","logo":{"@type":"ImageObject","@id":"https:\/\/wiki.edu.vn\/wiki4\/wp-content\/uploads\/2023\/08\/download.jpg","url":"https:\/\/wiki.edu.vn\/wiki4\/wp-content\/uploads\/2023\/08\/download.jpg","width":600,"height":60}},"image":{"@type":"ImageObject","@id":"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/9\/98\/Ambox_current_red.svg\/42px-Ambox_current_red.svg.png","url":"https:\/\/upload.wikimedia.org\/wikipedia\/commons\/thumb\/9\/98\/Ambox_current_red.svg\/42px-Ambox_current_red.svg.png","height":"34","width":"42"},"url":"https:\/\/wiki.edu.vn\/en\/list-of-mesh-codes-c18\/","wordCount":7852,"articleBody":"     (adsbygoogle = window.adsbygoogle || []).push({});before-content-x4From Wikipedia, the free encyclopedia       (adsbygoogle = window.adsbygoogle || []).push({});after-content-x4This article needs to be updated. The reason given is: no files for 2006 are listed at the cited source, but files for 2013 are there; NLM releases this information annually. Please help update this article to reflect recent events or newly available information.  (February 2020)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).       (adsbygoogle = window.adsbygoogle || []).push({});after-content-x4This list continues the information at List of MeSH codes (C17). Codes following these are found at List of MeSH codes (C19). For other MeSH codes, see List of MeSH codes.The source for this content is the set of 2006 MeSH Trees from the NLM.Table of Contents       (adsbygoogle = window.adsbygoogle || []).push({});after-content-x4MeSH\u00a0C18.452 \u2013 metabolic diseases[edit]MeSH\u00a0C18.452.076 \u2013 acid-base imbalance[edit]MeSH\u00a0C18.452.090 \u2013 amyloidosis[edit]MeSH\u00a0C18.452.100 \u2013 brain diseases, metabolic[edit]MeSH\u00a0C18.452.174 \u2013 calcium metabolism disorders[edit]MeSH\u00a0C18.452.284 \u2013 DNA repair-deficiency disorders[edit]MeSH\u00a0C18.452.339 \u2013 dyslipidemias[edit]MeSH\u00a0C18.452.394 \u2013 glucose metabolism disorders[edit]MeSH\u00a0C18.452.413 \u2013 hyperammonemia[edit]MeSH\u00a0C18.452.421 \u2013 hyperamylasemia[edit]MeSH\u00a0C18.452.429 \u2013 hyperbilirubinemia[edit]MeSH\u00a0C18.452.497 \u2013 hyperoxaluria[edit]MeSH\u00a0C18.452.500 \u2013 hyperprolactinemia[edit]MeSH\u00a0C18.452.506 \u2013 hyperuricemia[edit]MeSH\u00a0C18.452.512 \u2013 hypervitaminosis A[edit]MeSH\u00a0C18.452.565 \u2013 iron metabolism disorders[edit]MeSH\u00a0C18.452.603 \u2013 malabsorption syndromes[edit]MeSH\u00a0C18.452.625 \u2013 metabolic syndrome x[edit]MeSH\u00a0C18.452.648 \u2013 metabolism, inborn errors[edit]MeSH\u00a0C18.452.660 \u2013 mitochondrial diseases[edit]MeSH\u00a0C18.452.730 \u2013 ochronosis[edit]MeSH\u00a0C18.452.750 \u2013 phosphorus metabolism disorders[edit]MeSH\u00a0C18.452.872 \u2013 skin diseases, metabolic[edit]MeSH\u00a0C18.452.940 \u2013 wasting syndrome[edit]MeSH\u00a0C18.452.950 \u2013 water-electrolyte imbalance[edit]MeSH\u00a0C18.654 \u2013 nutrition disorders[edit]MeSH\u00a0C18.654.180 \u2013 child nutrition disorders[edit]MeSH\u00a0C18.654.422 \u2013 infant nutrition disorders[edit]MeSH\u00a0C18.654.521 \u2013 malnutrition[edit]MeSH\u00a0C18.654.726 \u2013 overnutrition[edit]MeSH\u00a0C18.654.940 \u2013 wasting syndrome[edit]MeSH\u00a0C18.452 \u2013 metabolic diseases[edit]MeSH\u00a0C18.452.076 \u2013 acid-base imbalance[edit]MeSH\u00a0C18.452.090 \u2013 amyloidosis[edit]MeSH\u00a0C18.452.100 \u2013 brain diseases, metabolic[edit]MeSH\u00a0C18.452.174 \u2013 calcium metabolism disorders[edit]MeSH\u00a0C18.452.284 \u2013 DNA repair-deficiency disorders[edit]MeSH\u00a0C18.452.339 \u2013 dyslipidemias[edit]MeSH\u00a0C18.452.394 \u2013 glucose metabolism disorders[edit]MeSH\u00a0C18.452.413 \u2013 hyperammonemia[edit]MeSH\u00a0C18.452.421 \u2013 hyperamylasemia[edit]MeSH\u00a0C18.452.429 \u2013 hyperbilirubinemia[edit]MeSH\u00a0C18.452.497 \u2013 hyperoxaluria[edit]MeSH\u00a0C18.452.500 \u2013 hyperprolactinemia[edit]MeSH\u00a0C18.452.506 \u2013 hyperuricemia[edit]MeSH\u00a0C18.452.512 \u2013 hypervitaminosis A[edit]MeSH\u00a0C18.452.565 \u2013 iron metabolism disorders[edit]MeSH\u00a0C18.452.603 \u2013 malabsorption syndromes[edit]MeSH\u00a0C18.452.625 \u2013 metabolic syndrome x[edit]MeSH\u00a0C18.452.648 \u2013 metabolism, inborn errors[edit]MeSH\u00a0C18.452.648.066 \u2013 amino acid metabolism, inborn errorsMeSH\u00a0C18.452.648.066.102 \u2013 albinismMeSH\u00a0C18.452.648.066.102.090 \u2013 albinism, ocularMeSH\u00a0C18.452.648.066.102.100 \u2013 albinism, oculocutaneousMeSH\u00a0C18.452.648.066.102.100.400 \u2013 Hermansky\u2013Pudlak syndromeMeSH\u00a0C18.452.648.066.102.600 \u2013 piebaldismMeSH\u00a0C18.452.648.066.187 \u2013 alkaptonuriaMeSH\u00a0C18.452.648.066.210 \u2013 aminoaciduria, renalMeSH\u00a0C18.452.648.066.210.250 \u2013 cystinuriaMeSH\u00a0C18.452.648.066.210.490 \u2013 Hartnup diseaseMeSH\u00a0C18.452.648.066.275 \u2013 carbamoyl phosphate synthase I deficiency diseaseMeSH\u00a0C18.452.648.066.340 \u2013 citrullinemiaMeSH\u00a0C18.452.648.066.470 \u2013 homocystinuriaMeSH\u00a0C18.452.648.066.475 \u2013 hyperargininemiaMeSH\u00a0C18.452.648.066.477 \u2013 hyperglycinemia, nonketoticMeSH\u00a0C18.452.648.066.480 \u2013 hyperhomocysteinemiaMeSH\u00a0C18.452.648.066.544 \u2013 hyperlysinemiasMeSH\u00a0C18.452.648.066.608 \u2013 maple syrup urine diseaseMeSH\u00a0C18.452.648.066.620 \u2013 multiple carboxylase deficiencyMeSH\u00a0C18.452.648.066.620.100 \u2013 biotinidase deficiencyMeSH\u00a0C18.452.648.066.620.380 \u2013 holocarboxylase synthetase deficiencyMeSH\u00a0C18.452.648.066.729 \u2013 ornithine carbamoyltransferase deficiency diseaseMeSH\u00a0C18.452.648.066.766 \u2013 phenylketonuriasMeSH\u00a0C18.452.648.066.766.500 \u2013 phenylketonuria, maternalMeSH\u00a0C18.452.648.066.880 \u2013 tyrosinemiasMeSH\u00a0C18.452.648.088 \u2013 amino acid transport disorders, inbornMeSH\u00a0C18.452.648.088.400 \u2013 hartnup diseaseMeSH\u00a0C18.452.648.088.600 \u2013 oculocerebrorenal syndromeMeSH\u00a0C18.452.648.100 \u2013 amyloidosis, familialMeSH\u00a0C18.452.648.100.050 \u2013 amyloid neuropathies, familialMeSH\u00a0C18.452.648.100.160 \u2013 cerebral amyloid angiopathy, familialMeSH\u00a0C18.452.648.151 \u2013 brain diseases, metabolic, inbornMeSH\u00a0C18.452.648.151.050 \u2013 abetalipoproteinemiaMeSH\u00a0C18.452.648.151.162 \u2013 carbamoyl-phosphate synthase i deficiency diseaseMeSH\u00a0C18.452.648.151.168 \u2013 cerebral amyloid angiopathy, familialMeSH\u00a0C18.452.648.151.175 \u2013 citrullinemiaMeSH\u00a0C18.452.648.151.300 \u2013 fucosidosisMeSH\u00a0C18.452.648.151.320 \u2013 galactosemiasMeSH\u00a0C18.452.648.151.330 \u2013 glycogen storage disease type IIMeSH\u00a0C18.452.648.151.355 \u2013 hartnup diseaseMeSH\u00a0C18.452.648.151.360 \u2013 hepatolenticular degenerationMeSH\u00a0C18.452.648.151.365 \u2013 homocystinuriaMeSH\u00a0C18.452.648.151.370 \u2013 hyperargininemiaMeSH\u00a0C18.452.648.151.375 \u2013 hyperglycinemia, nonketoticMeSH\u00a0C18.452.648.151.380 \u2013 hyperlysinemiasMeSH\u00a0C18.452.648.151.412 \u2013 Leigh diseaseMeSH\u00a0C18.452.648.151.425 \u2013 Lesch\u2013Nyhan syndromeMeSH\u00a0C18.452.648.151.435 \u2013 lysosomal storage diseases, nervous systemMeSH\u00a0C18.452.648.151.435.295 \u2013 fucosidosisMeSH\u00a0C18.452.648.151.435.340 \u2013 glycogen storage disease type IIMeSH\u00a0C18.452.648.151.435.590 \u2013 mucolipidosesMeSH\u00a0C18.452.648.151.435.810 \u2013 sialic acid storage diseaseMeSH\u00a0C18.452.648.151.435.825 \u2013 sphingolipidosesMeSH\u00a0C18.452.648.151.435.825.200 \u2013 Fabry diseaseMeSH\u00a0C18.452.648.151.435.825.300 \u2013 gangliosidosesMeSH\u00a0C18.452.648.151.435.825.300.300 \u2013 gangliosidoses GM2MeSH\u00a0C18.452.648.151.435.825.300.300.800 \u2013 Sandhoff diseaseMeSH\u00a0C18.452.648.151.435.825.300.300.840 \u2013 Tay\u2013Sachs diseaseMeSH\u00a0C18.452.648.151.435.825.300.300.920 \u2013 Tay\u2013Sachs disease, AB variantMeSH\u00a0C18.452.648.151.435.825.300.400 \u2013 gangliosidosis gm1MeSH\u00a0C18.452.648.151.435.825.400 \u2013 Gaucher diseaseMeSH\u00a0C18.452.648.151.435.825.590 \u2013 leukodystrophy, globoid cellMeSH\u00a0C18.452.648.151.435.825.594 \u2013 leukodystrophy, metachromaticMeSH\u00a0C18.452.648.151.435.825.700 \u2013 Niemann\u2013Pick diseasesMeSH\u00a0C18.452.648.151.445 \u2013 maple syrup urine diseaseMeSH\u00a0C18.452.648.151.447 \u2013 MELAS syndromeMeSH\u00a0C18.452.648.151.450 \u2013 menkes kinky hair syndromeMeSH\u00a0C18.452.648.151.505 \u2013 MERRF syndromeMeSH\u00a0C18.452.648.151.580 \u2013 mucolipidosesMeSH\u00a0C18.452.648.151.640 \u2013 oculocerebrorenal syndromeMeSH\u00a0C18.452.648.151.650 \u2013 ornithine carbamoyltransferase deficiency diseaseMeSH\u00a0C18.452.648.151.680 \u2013 peroxisomal disordersMeSH\u00a0C18.452.648.151.680.100 \u2013 adrenoleukodystrophyMeSH\u00a0C18.452.648.151.680.760 \u2013 refsum diseaseMeSH\u00a0C18.452.648.151.680.970 \u2013 Zellweger syndromeMeSH\u00a0C18.452.648.151.687 \u2013 phenylketonuriasMeSH\u00a0C18.452.648.151.687.500 \u2013 phenylketonuria, maternalMeSH\u00a0C18.452.648.151.725 \u2013 pyruvate carboxylase deficiency diseaseMeSH\u00a0C18.452.648.151.750 \u2013 pyruvate dehydrogenase complex deficiency diseaseMeSH\u00a0C18.452.648.151.825 \u2013 sphingolipidosesMeSH\u00a0C18.452.648.151.825.200 \u2013 Fabry diseaseMeSH\u00a0C18.452.648.151.825.300 \u2013 gangliosidosesMeSH\u00a0C18.452.648.151.825.300.300 \u2013 gangliosidoses gm2MeSH\u00a0C18.452.648.151.825.300.300.700 \u2013 Sandhoff diseaseMeSH\u00a0C18.452.648.151.825.300.300.850 \u2013 Tay\u2013Sachs diseaseMeSH\u00a0C18.452.648.151.825.300.300.925 \u2013 Tay\u2013Sachs disease, AB variantMeSH\u00a0C18.452.648.151.825.300.400 \u2013 gangliosidosis gm1MeSH\u00a0C18.452.648.151.825.400 \u2013 Gaucher diseaseMeSH\u00a0C18.452.648.151.825.590 \u2013 leukodystrophy, globoid cellMeSH\u00a0C18.452.648.151.825.594 \u2013 leukodystrophy, metachromaticMeSH\u00a0C18.452.648.151.825.700 \u2013 Niemann\u2013Pick diseasesMeSH\u00a0C18.452.648.151.875 \u2013 tyrosinemiasMeSH\u00a0C18.452.648.202 \u2013 carbohydrate metabolism, inborn errorsMeSH\u00a0C18.452.648.202.125 \u2013 carbohydrate-deficient glycoprotein syndromeMeSH\u00a0C18.452.648.202.251 \u2013 fructose metabolism, inborn errorsMeSH\u00a0C18.452.648.202.251.221 \u2013 fructose-1,6-diphosphatase deficiencyMeSH\u00a0C18.452.648.202.251.271 \u2013 Hereditary fructose intoleranceMeSH\u00a0C18.452.648.202.303 \u2013 fucosidosisMeSH\u00a0C18.452.648.202.355 \u2013 galactosemiasMeSH\u00a0C18.452.648.202.449 \u2013 glycogen storage diseaseMeSH\u00a0C18.452.648.202.449.448 \u2013 glycogen storage disease type IMeSH\u00a0C18.452.648.202.449.500 \u2013 glycogen storage disease type IIMeSH\u00a0C18.452.648.202.449.510 \u2013 glycogen storage disease type IIbMeSH\u00a0C18.452.648.202.449.520 \u2013 glycogen storage disease type IIIMeSH\u00a0C18.452.648.202.449.540 \u2013 glycogen storage disease type IVMeSH\u00a0C18.452.648.202.449.560 \u2013 glycogen storage disease type VMeSH\u00a0C18.452.648.202.449.580 \u2013 glycogen storage disease type VIMeSH\u00a0C18.452.648.202.449.600 \u2013 glycogen storage disease type VIIMeSH\u00a0C18.452.648.202.449.620 \u2013 glycogen storage disease type VIIIMeSH\u00a0C18.452.648.202.460 \u2013 hyperoxaluria, primaryMeSH\u00a0C18.452.648.202.589 \u2013 lactose intoleranceMeSH\u00a0C18.452.648.202.607 \u2013 mannosidase deficiency diseasesMeSH\u00a0C18.452.648.202.607.500 \u2013 alpha-mannosidosisMeSH\u00a0C18.452.648.202.607.750 \u2013 beta-mannosidosisMeSH\u00a0C18.452.648.202.670 \u2013 mucolipidosesMeSH\u00a0C18.452.648.202.715 \u2013 mucopolysaccharidosesMeSH\u00a0C18.452.648.202.715.640 \u2013 mucopolysaccharidosis IMeSH\u00a0C18.452.648.202.715.645 \u2013 mucopolysaccharidosis IIMeSH\u00a0C18.452.648.202.715.650 \u2013 mucopolysaccharidosis IIIMeSH\u00a0C18.452.648.202.715.655 \u2013 mucopolysaccharidosis IVMeSH\u00a0C18.452.648.202.715.670 \u2013 mucopolysaccharidosis VIMeSH\u00a0C18.452.648.202.715.675 \u2013 mucopolysaccharidosis VIIMeSH\u00a0C18.452.648.202.720 \u2013 multiple carboxylase deficiencyMeSH\u00a0C18.452.648.202.720.100 \u2013 biotinidase deficiencyMeSH\u00a0C18.452.648.202.720.380 \u2013 holocarboxylase synthetase deficiencyMeSH\u00a0C18.452.648.202.810 \u2013 pyruvate metabolism, inborn errorsMeSH\u00a0C18.452.648.202.810.444 \u2013 Leigh diseaseMeSH\u00a0C18.452.648.202.810.666 \u2013 pyruvate carboxylase deficiency diseaseMeSH\u00a0C18.452.648.202.810.766 \u2013 pyruvate dehydrogenase complex deficiency diseaseMeSH\u00a0C18.452.648.240 \u2013 cytochrome-c oxidase deficiencyMeSH\u00a0C18.452.648.390 \u2013 glucosephosphate dehydrogenase deficiencyMeSH\u00a0C18.452.648.437 \u2013 hyperbilirubinemia, hereditaryMeSH\u00a0C18.452.648.437.281 \u2013 Crigler\u2013Najjar syndromeMeSH\u00a0C18.452.648.437.528 \u2013 gilbert diseaseMeSH\u00a0C18.452.648.499 \u2013 jaundice, chronic idiopathicMeSH\u00a0C18.452.648.556 \u2013 lipid metabolism, inborn errorsMeSH\u00a0C18.452.648.556.475 \u2013 hypercholesterolemia, familialMeSH\u00a0C18.452.648.556.480 \u2013 hyperlipidemia, familial combinedMeSH\u00a0C18.452.648.556.480.390 \u2013 hypercholesterolemia, familialMeSH\u00a0C18.452.648.556.480.395 \u2013 hyperlipoproteinemia type IVMeSH\u00a0C18.452.648.556.484 \u2013 hyperlipoproteinemia type IIIMeSH\u00a0C18.452.648.556.490 \u2013 hyperlipoproteinemia type IVMeSH\u00a0C18.452.648.556.495 \u2013 hyperlipoproteinemia type VMeSH\u00a0C18.452.648.556.500 \u2013 hypolipoproteinemiaMeSH\u00a0C18.452.648.556.500.220 \u2013 abetalipoproteinemiaMeSH\u00a0C18.452.648.556.500.440 \u2013 hypobetalipoproteinemiaMeSH\u00a0C18.452.648.556.500.448 \u2013 lecithin acyltransferase deficiencyMeSH\u00a0C18.452.648.556.500.724 \u2013 Tangier diseaseMeSH\u00a0C18.452.648.556.641 \u2013 lipoidosisMeSH\u00a0C18.452.648.556.641.201 \u2013 cholesterol ester storage diseaseMeSH\u00a0C18.452.648.556.641.391 \u2013 lipoidproteinosisMeSH\u00a0C18.452.648.556.641.509 \u2013 neuronal ceroid lipofuscinosisMeSH\u00a0C18.452.648.556.641.643 \u2013 Refsum diseaseMeSH\u00a0C18.452.648.556.641.723 \u2013 Sj\u00f6gren\u2013Larsson syndromeMeSH\u00a0C18.452.648.556.641.803 \u2013 sphingolipidosesMeSH\u00a0C18.452.648.556.641.803.300 \u2013 Fabry diseaseMeSH\u00a0C18.452.648.556.641.803.350 \u2013 gangliosidosesMeSH\u00a0C18.452.648.556.641.803.350.300 \u2013 gangliosidoses GM2MeSH\u00a0C18.452.648.556.641.803.350.300.700 \u2013 Sandhoff diseaseMeSH\u00a0C18.452.648.556.641.803.350.300.850 \u2013 Tay\u2013Sachs diseaseMeSH\u00a0C18.452.648.556.641.803.350.300.925 \u2013 Tay\u2013Sachs disease, AB variantMeSH\u00a0C18.452.648.556.641.803.350.360 \u2013 gangliosidosis gm1MeSH\u00a0C18.452.648.556.641.803.441 \u2013 Gaucher diseaseMeSH\u00a0C18.452.648.556.641.803.585 \u2013 leukodystrophy, globoid cellMeSH\u00a0C18.452.648.556.641.803.594 \u2013 leukodystrophy, metachromaticMeSH\u00a0C18.452.648.556.641.803.730 \u2013 Niemann\u2013Pick diseasesMeSH\u00a0C18.452.648.556.641.803.850 \u2013 sea-blue histiocyte syndromeMeSH\u00a0C18.452.648.556.641.923 \u2013 Wolman diseaseMeSH\u00a0C18.452.648.556.645 \u2013 lipoprotein lipase deficiency, familialMeSH\u00a0C18.452.648.556.750 \u2013 peroxisomal disordersMeSH\u00a0C18.452.648.556.750.025 \u2013 acatalasiaMeSH\u00a0C18.452.648.556.750.112 \u2013 adrenoleukodystrophyMeSH\u00a0C18.452.648.556.750.200 \u2013 chondrodysplasia punctata, rhizomelicMeSH\u00a0C18.452.648.556.750.760 \u2013 Refsum diseaseMeSH\u00a0C18.452.648.556.750.970 \u2013 Zellweger syndromeMeSH\u00a0C18.452.648.556.850 \u2013 Smith\u2013Lemli\u2013Opitz syndromeMeSH\u00a0C18.452.648.556.925 \u2013 xanthomatosis, cerebrotendinousMeSH\u00a0C18.452.648.595 \u2013 lysosomal storage diseasesMeSH\u00a0C18.452.648.595.201 \u2013 cholesterol ester storage diseaseMeSH\u00a0C18.452.648.595.554 \u2013 lysosomal storage diseases, nervous systemMeSH\u00a0C18.452.648.595.554.295 \u2013 fucosidosisMeSH\u00a0C18.452.648.595.554.340 \u2013 glycogen storage disease type IIMeSH\u00a0C18.452.648.595.554.590 \u2013 mucolipidosesMeSH\u00a0C18.452.648.595.554.810 \u2013 sialic acid storage diseaseMeSH\u00a0C18.452.648.595.554.825 \u2013 sphingolipidosesMeSH\u00a0C18.452.648.595.554.825.200 \u2013 Fabry diseaseMeSH\u00a0C18.452.648.595.554.825.300 \u2013 gangliosidosesMeSH\u00a0C18.452.648.595.554.825.300.300 \u2013 gangliosidoses GM2MeSH\u00a0C18.452.648.595.554.825.300.300.800 \u2013 Sandhoff diseaseMeSH\u00a0C18.452.648.595.554.825.300.300.840 \u2013 Tay\u2013Sachs diseaseMeSH\u00a0C18.452.648.595.554.825.300.300.920 \u2013 Tay\u2013Sachs disease, AB variantMeSH\u00a0C18.452.648.595.554.825.300.400 \u2013 gangliosidosis gm1MeSH\u00a0C18.452.648.595.554.825.400 \u2013 Gaucher diseaseMeSH\u00a0C18.452.648.595.554.825.590 \u2013 leukodystrophy, globoid cellMeSH\u00a0C18.452.648.595.554.825.594 \u2013 leukodystrophy, metachromaticMeSH\u00a0C18.452.648.595.554.825.700 \u2013 Niemann\u2013Pick diseasesMeSH\u00a0C18.452.648.595.577 \u2013 mannosidase deficiency diseasesMeSH\u00a0C18.452.648.595.577.500 \u2013 alpha-mannosidosisMeSH\u00a0C18.452.648.595.577.750 \u2013 beta-mannosidosisMeSH\u00a0C18.452.648.595.600 \u2013 mucopolysaccharidosesMeSH\u00a0C18.452.648.595.600.640 \u2013 mucopolysaccharidosis IMeSH\u00a0C18.452.648.595.600.645 \u2013 mucopolysaccharidosis IIMeSH\u00a0C18.452.648.595.600.650 \u2013 mucopolysaccharidosis IIIMeSH\u00a0C18.452.648.595.600.655 \u2013 mucopolysaccharidosis IVMeSH\u00a0C18.452.648.595.600.670 \u2013 mucopolysaccharidosis VIMeSH\u00a0C18.452.648.595.600.675 \u2013 mucopolysaccharidosis VIIMeSH\u00a0C18.452.648.595.803 \u2013 sphingolipidosesMeSH\u00a0C18.452.648.595.803.300 \u2013 Fabry diseaseMeSH\u00a0C18.452.648.595.803.350 \u2013 gangliosidosesMeSH\u00a0C18.452.648.595.803.350.300 \u2013 gangliosidoses GM2MeSH\u00a0C18.452.648.595.803.350.300.700 \u2013 Sandhoff diseaseMeSH\u00a0C18.452.648.595.803.350.300.850 \u2013 Tay\u2013Sachs diseaseMeSH\u00a0C18.452.648.595.803.350.300.925 \u2013 Tay\u2013Sachs disease, AB variantMeSH\u00a0C18.452.648.595.803.441 \u2013 Gaucher diseaseMeSH\u00a0C18.452.648.595.803.585 \u2013 leukodystrophy, globoid cellMeSH\u00a0C18.452.648.595.803.594 \u2013 leukodystrophy, metachromaticMeSH\u00a0C18.452.648.595.803.730 \u2013 Niemann\u2013Pick diseasesMeSH\u00a0C18.452.648.595.803.850 \u2013 sea-blue histiocyte syndromeMeSH\u00a0C18.452.648.595.923 \u2013 Wolman diseaseMeSH\u00a0C18.452.648.618 \u2013 metal metabolism, inborn errorsMeSH\u00a0C18.452.648.618.337 \u2013 hemochromatosisMeSH\u00a0C18.452.648.618.403 \u2013 hepatolenticular degenerationMeSH\u00a0C18.452.648.618.482 \u2013 hypophosphatasiaMeSH\u00a0C18.452.648.618.544 \u2013 hypophosphatemia, familialMeSH\u00a0C18.452.648.618.590 \u2013 Menkes kinky hair syndromeMeSH\u00a0C18.452.648.618.711 \u2013 paralyses, familial periodicMeSH\u00a0C18.452.648.618.711.550 \u2013 hypokalemic periodic paralysisMeSH\u00a0C18.452.648.618.711.600 \u2013 paralysis, hyperkalemic periodicMeSH\u00a0C18.452.648.618.815 \u2013 pseudohypoparathyroidismMeSH\u00a0C18.452.648.618.815.815 \u2013 pseudopseudohypoparathyroidismMeSH\u00a0C18.452.648.730 \u2013 porphyria, erythropoieticMeSH\u00a0C18.452.648.735 \u2013 porphyrias, hepaticMeSH\u00a0C18.452.648.735.074 \u2013 coproporphyria, hereditaryMeSH\u00a0C18.452.648.735.150 \u2013 porphyria, acute intermittentMeSH\u00a0C18.452.648.735.250 \u2013 porphyria cutanea tardaMeSH\u00a0C18.452.648.735.437 \u2013 porphyria, hepatoerythropoieticMeSH\u00a0C18.452.648.735.625 \u2013 porphyria, variegateMeSH\u00a0C18.452.648.735.812 \u2013 protoporphyria, erythropoieticMeSH\u00a0C18.452.648.769 \u2013 progeriaMeSH\u00a0C18.452.648.798 \u2013 purine\u2013pyrimidine metabolism, inborn errorsMeSH\u00a0C18.452.648.798.368 \u2013 goutMeSH\u00a0C18.452.648.798.368.410 \u2013 arthritis, goutyMeSH\u00a0C18.452.648.798.594 \u2013 Lesch\u2013Nyhan syndromeMeSH\u00a0C18.452.648.851 \u2013 renal tubular transport, inborn errorsMeSH\u00a0C18.452.648.851.093 \u2013 acidosis, renal tubularMeSH\u00a0C18.452.648.851.191 \u2013 aminoaciduria, renalMeSH\u00a0C18.452.648.851.191.250 \u2013 cystinuriaMeSH\u00a0C18.452.648.851.191.457 \u2013 Hartnup diseaseMeSH\u00a0C18.452.648.851.368 \u2013 cystinosisMeSH\u00a0C18.452.648.851.368.210 \u2013 Fanconi syndromeMeSH\u00a0C18.452.648.851.532 \u2013 glycosuria, renalMeSH\u00a0C18.452.648.851.647 \u2013 hypophosphatemia, familialMeSH\u00a0C18.452.648.851.750 \u2013 oculocerebrorenal syndromeMeSH\u00a0C18.452.648.851.770 \u2013 pseudohypoaldosteronismMeSH\u00a0C18.452.648.925 \u2013 steroid metabolism, inborn errorsMeSH\u00a0C18.452.648.925.249 \u2013 adrenal hyperplasia, congenitalMeSH\u00a0C18.452.648.925.500 \u2013 mineralocorticoid excess syndrome, apparentMeSH\u00a0C18.452.648.925.750 \u2013 ichthyosis, x-linkedMeSH\u00a0C18.452.648.925.875 \u2013 Smith\u2013Lemli\u2013Opitz syndromeMeSH\u00a0C18.452.660 \u2013 mitochondrial diseases[edit]MeSH\u00a0C18.452.730 \u2013 ochronosis[edit]MeSH\u00a0C18.452.750 \u2013 phosphorus metabolism disorders[edit]MeSH\u00a0C18.452.872 \u2013 skin diseases, metabolic[edit]MeSH\u00a0C18.452.940 \u2013 wasting syndrome[edit]MeSH\u00a0C18.452.950 \u2013 water-electrolyte imbalance[edit]MeSH\u00a0C18.654 \u2013 nutrition disorders[edit]MeSH\u00a0C18.654.180 \u2013 child nutrition disorders[edit]MeSH\u00a0C18.654.422 \u2013 infant nutrition disorders[edit]MeSH\u00a0C18.654.521 \u2013 malnutrition[edit]MeSH\u00a0C18.654.726 \u2013 overnutrition[edit]MeSH\u00a0C18.654.940 \u2013 wasting syndrome[edit]The list continues at List of MeSH codes (C19).     (adsbygoogle = window.adsbygoogle || []).push({});after-content-x4"},{"@context":"http:\/\/schema.org\/","@type":"BreadcrumbList","itemListElement":[{"@type":"ListItem","position":1,"item":{"@id":"https:\/\/wiki.edu.vn\/en\/#breadcrumbitem","name":"Enzyklop\u00e4die"}},{"@type":"ListItem","position":2,"item":{"@id":"https:\/\/wiki.edu.vn\/en\/list-of-mesh-codes-c18\/#breadcrumbitem","name":"List of MeSH codes (C18)"}}]}]