Lista över MeSH-koder (C18)

Följande är en ofullständig lista över "C"-koderna för medicinska ämnesrubriker (MeSH), enligt definition av United States National Library of Medicine (NLM).

Denna lista fortsätter informationen på Lista över MeSH-koder (C17) . Koder som följer dessa finns i Lista över MeSH-koder (C19) . För andra MeSH-koder, se Lista över MeSH-koder .

Källan för detta innehåll är uppsättningen 2006 MeSH Trees från NLM.

MeSH C18 – närings- och metabola sjukdomar

MeSH C18.452 – metabola sjukdomar

MeSH C18.452.076 – syra-bas obalans

MeSH C18.452.076.087 – achlorhydria
MeSH C18.452.076.176 – acidos
MeSH C18.452.076.176.180 – acidos, mjölksyra
MeSH C18.452.076.176.210 – acidos, renal tubulär
MeSH C18.452.076.176.310 – acidos, andningsvägar
MeSH C18.452.076.176.390 – diabetisk ketoacidos
MeSH C18.452.076.176.652 – ketos
MeSH C18.452.076.354 – alkalos
MeSH C18.452.076.354.271 – alkalos, andningsvägar

MeSH C18.452.090 – amyloidos

MeSH C18.452.090.050 – amyloida neuropatier
MeSH C18.452.090.050.050 – amyloida neuropatier, familjär
MeSH C18.452.090.075 – amyloidos, familjär
MeSH C18.452.090.075.050 – amyloida neuropatier, familjär
MeSH C18.452.090.075.160 – cerebral amyloidangiopati, familjär
MeSH C18.452.090.100 – cerebral amyloidangiopati
MeSH C18.452.090.100.160 – cerebral amyloidangiopati, familjär

MeSH C18.452.100 – hjärnsjukdomar, metabola

MeSH C18.452.100.100 – hjärnsjukdomar, metabola, medfödda
MeSH C18.452.100.100.050 – abetalipoproteinemi
MeSH C18.452.100.100.162 – karbamoyl-fosfatsyntas I-bristsjukdom
MeSH C18.452.100.100.175 – citrullinemi
MeSH C18.452.100.100.320 – galaktosemi
MeSH C18.452.100.100.355 – Hartnups sjukdom
MeSH C18.452.100.100.360 – hepatolentikulär degeneration
MeSH C18.452.100.100.365 – homocystinuri
MeSH C18.452.100.100.370 – hyperargininemi
MeSH C18.452.100.100.375 – hyperglycinemi, icke-ketotisk
MeSH C18.452.100.100.380 – hyperlysinemier
MeSH C18.452.100.100.412 – Leigh sjukdom
MeSH C18.452.100.100.425 – Lesch–Nyhans syndrom
MeSH C18.452.100.100.435 – lysosomala lagringssjukdomar, nervsystemet
MeSH C18.452.100.100.435.295 – fucosidos
MeSH C18.452.100.100.435.340 – glykogenlagringssjukdom typ II
MeSH C18.452.100.100.435.590 – mukolipidoser
MeSH C18.452.100.100.435.810 – sialinsyralagringssjukdom
MeSH C18.452.100.100.435.825 – sfingolipidoser
MeSH C18.452.100.100.435.825.200 – Fabry sjukdom
MeSH C18.452.100.100.435.825.300 – gangliosidoser
MeSH C18.452.100.100.435.825.300.300 – gangliosidoser GM2
MeSH C18.452.100.100.435.825.300.300.800 – Sandhoffs sjukdom
MeSH C18.452.100.100.435.825.300.300.840 – Tay–Sachs sjukdom
MeSH C18.452.100.100.435.825.300.300.920 – Tay–Sachs sjukdom, AB-variant
MeSH C18.452.100.100.435.825.300.400 – gangliosidos gm1
MeSH C18.452.100.100.435.825.400 – Gauchers sjukdom
MeSH C18.452.100.100.435.825.590 – leukodystrofi, globoidcell
MeSH C18.452.100.100.435.825.594 – leukodystrofi, metakromatisk
MeSH C18.452.100.100.435.825.700 – Niemann–Pick sjukdomar
MeSH C18.452.100.100.520 – lönnsirapsurinsjukdom
MeSH C18.452.100.100.535 – MELAS syndrom
MeSH C18.452.100.100.540 – Menkes kinky hair syndrome
MeSH C18.452.100.100.545 – MERRF-syndrom
MeSH C18.452.100.100.640 – oculocerebrorenalt syndrom
MeSH C18.452.100.100.650 – ornitinkarbamoyltransferasbristsjukdom
MeSH C18.452.100.100.680 – peroxisomala störningar
MeSH C18.452.100.100.680.100 – adrenoleukodystrofi
MeSH C18.452.100.100.680.760 – Refsum sjukdom
MeSH C18.452.100.100.680.970 – Zellwegers syndrom
MeSH C18.452.100.100.687 – fenylketonuri
MeSH C18.452.100.100.687.500 – fenylketonuri, modern
MeSH C18.452.100.100.725 – pyruvatkarboxylasbristsjukdom
MeSH C18.452.100.100.750 – pyruvatdehydrogenaskomplexbristsjukdom
MeSH C18.452.100.100.875 – tyrosinemier
MeSH C18.452.100.360 – hepatisk encefalopati
MeSH C18.452.100.480 – kernicterus
MeSH C18.452.100.540 – mitokondriella encefalomyopatier
MeSH C18.452.100.560 – myelinolys, central pontine
MeSH C18.452.100.780 – Reyes syndrom
MeSH C18.452.100.960 – Wernicke-encefalopati

MeSH C18.452.174 – störningar i kalciummetabolismen

MeSH C18.452.174.130 – kalcinos
MeSH C18.452.174.130.186 – kalcifylax
MeSH C18.452.174.130.204 – CREST syndrom
MeSH C18.452.174.130.560 – nefrokalcinos
MeSH C18.452.174.289 – avkalkning, patologisk
MeSH C18.452.174.451 – hyperkalcemi
MeSH C18.452.174.509 – hypokalcemi
MeSH C18.452.174.509.700 – tetany
MeSH C18.452.174.662 – osteomalaci
MeSH C18.452.174.766 – pseudohypoparatyreos
MeSH C18.452.174.766.815 – pseudopseudohypoparatyreos
MeSH C18.452.174.845 – rakitis

MeSH C18.452.284 – DNA-reparationsbriststörningar

MeSH C18.452.284.060 – ataxi–telangiektasi
MeSH C18.452.284.100 – Blooms syndrom
MeSH C18.452.284.250 – Cockayne syndrom
MeSH C18.452.284.255 – kolorektala neoplasmer, ärftlig icke-polypos
MeSH C18.452.284.280 – fanconi-anemi
MeSH C18.452.284.520 – Li–Fraumeni syndrom
MeSH C18.452.284.600 – Nijmegens brottsyndrom
MeSH C18.452.284.760 – Rothmund–Thomsons syndrom
MeSH C18.452.284.800 – svår kombinerad immunbrist
MeSH C18.452.284.960 – Werners syndrom
MeSH C18.452.284.975 – xeroderma pigmentosum

MeSH C18.452.339 – dyslipidemier

MeSH C18.452.339.500 – hyperlipidemi
MeSH C18.452.339.500.396 – hyperkolesterolemi
MeSH C18.452.339.500.396.300 – hyperkolesterolemi, familjär
MeSH C18.452.339.500.438 – hyperlipidemi, familjär kombinerad
MeSH C18.452.339.500.438.390 – hyperkolesterolemi, familjär
MeSH C18.452.339.500.438.395 – hyperlipoproteinemi typ IV
MeSH C18.452.339.500.851 – hypertriglyceridemi
MeSH C18.452.339.750 – hyperlipoproteinemi
MeSH C18.452.339.750.475 – hyperkolesterolemi, familjär
MeSH C18.452.339.750.485 – hyperlipoproteinemi typ III
MeSH C18.452.339.750.490 – hyperlipoproteinemi typ IV
MeSH C18.452.339.750.495 – hyperlipoproteinemi typ V
MeSH C18.452.339.750.552 – lipoproteinlipasbrist, familjär
MeSH C18.452.339.875 – hypolipoproteinemi
MeSH C18.452.339.875.220 – abetalipoproteinemi
MeSH C18.452.339.875.440 – hypobetalipoproteinemi
MeSH C18.452.339.875.448 – lecitinacyltransferasbrist
MeSH C18.452.339.875.724 – tangier sjukdom

MeSH C18.452.394 – glukosmetabolismstörningar

MeSH C18.452.394.750 – diabetes mellitus
MeSH C18.452.394.750.074 – diabetes mellitus, experimentell
MeSH C18.452.394.750.124 – diabetes mellitus, typ 1
MeSH C18.452.394.750.124.960 – wolframs syndrom
MeSH C18.452.394.750.149 – diabetes mellitus, typ 2
MeSH C18.452.394.750.149.500 – diabetes mellitus, lipoatrof
MeSH C18.452.394.750.448 – diabetes, graviditet
MeSH C18.452.394.750.535 – diabetisk ketoacidos
MeSH C18.452.394.750.774 – prediabetiskt tillstånd
MeSH C18.452.394.937 – glykosuri
MeSH C18.452.394.937.450 – glykosuri, njure
MeSH C18.452.394.952 – hyperglykemi
MeSH C18.452.394.952.500 – glukosintolerans
MeSH C18.452.394.968 – hyperinsulinism
MeSH C18.452.394.968.500 – insulinresistens
MeSH C18.452.394.968.500.570 – metabolt syndrom x
MeSH C18.452.394.968.750 – ihållande hyperinsulinemi hypoglykemi i spädbarnsåldern
MeSH C18.452.394.984 – hypoglykemi
MeSH C18.452.394.984.492 – insulinkoma
MeSH C18.452.394.984.746 – ihållande hyperinsulinemi hypoglykemi i spädbarnsåldern

MeSH C18.452.413 – hyperammonemi

MeSH C18.452.421 – hyperamylasemi

MeSH C18.452.429 – hyperbilirubinemi

MeSH C18.452.429.124 – hyperbilirubinemi, neonatal
MeSH C18.452.429.124.500 – gulsot, neonatal
MeSH C18.452.429.500 – kernicterus

MeSH C18.452.497 – hyperoxaluri

MeSH C18.452.497.490 – hyperoxaluri, primär

MeSH C18.452.500 – hyperprolaktinemi

MeSH C18.452.506 – hyperurikemi

MeSH C18.452.512 – hypervitaminos A

MeSH C18.452.565 – störningar i järnmetabolismen

MeSH C18.452.565.100 – anemi, järnbrist
MeSH C18.452.565.500 – överbelastning av järn
MeSH C18.452.565.500.480 – hemokromatos
MeSH C18.452.565.500.500 – hemosideros

MeSH C18.452.603 – malabsorptionssyndrom

MeSH C18.452.603.145 – blind loop syndrom
MeSH C18.452.603.250 – celiaki
MeSH C18.452.603.506 – laktosintolerans
MeSH C18.452.603.850 – sprue, tropisk
MeSH C18.452.603.887 – steatorré
MeSH C18.452.603.925 – whipple sjukdom

MeSH C18.452.625 – metabolt syndrom x

MeSH C18.452.648 – metabolism, medfödda fel

MeSH C18.452.648.066 – aminosyrametabolism, medfödda fel
MeSH C18.452.648.066.102 – albinism
MeSH C18.452.648.066.102.090 – albinism, okulär
MeSH C18.452.648.066.102.100 – albinism, oculocutaneous
MeSH C18.452.648.066.102.100.400 – Hermansky–Pudlaks syndrom
MeSH C18.452.648.066.102.600 – piebaldism
MeSH C18.452.648.066.187 – alkaptonuri
MeSH C18.452.648.066.210 – aminoaciduri, renal
MeSH C18.452.648.066.210.250 – cystinuri
MeSH C18.452.648.066.210.490 – Hartnups sjukdom
MeSH C18.452.648.066.275 – karbamoylfosfatsyntas I-bristsjukdom
MeSH C18.452.648.066.340 – citrullinemi
MeSH C18.452.648.066.470 – homocystinuri
MeSH C18.452.648.066.475 – hyperargininemi
MeSH C18.452.648.066.477 – hyperglycinemi, icke-ketotisk
MeSH C18.452.648.066.480 – hyperhomocysteinemi
MeSH C18.452.648.066.544 – hyperlysinemier
MeSH C18.452.648.066.608 – lönnsirapsurinsjukdom
MeSH C18.452.648.066.620 – multipel karboxylasbrist
MeSH C18.452.648.066.620.100 – biotinidasbrist
MeSH C18.452.648.066.620.380 – holokarboxylassyntetasbrist
MeSH C18.452.648.066.729 – ornitinkarbamoyltransferasbristsjukdom
MeSH C18.452.648.066.766 – fenylketonuri
MeSH C18.452.648.066.766.500 – fenylketonuri, modern
MeSH C18.452.648.066.880 – tyrosinemier
MeSH C18.452.648.088 – aminosyratransportstörningar, medfödda
MeSH C18.452.648.088.400 – hartnup sjukdom
MeSH C18.452.648.088.600 – oculocerebrorenalt syndrom
MeSH C18.452.648.100 – amyloidos, familjär
MeSH C18.452.648.100.050 – amyloida neuropatier, familjär
MeSH C18.452.648.100.160 – cerebral amyloidangiopati, familjär
MeSH C18.452.648.151 – hjärnsjukdomar, metabola, medfödda
MeSH C18.452.648.151.050 – abetalipoproteinemi
MeSH C18.452.648.151.162 – karbamoylfosfatsyntas-i-bristsjukdom
MeSH C18.452.648.151.168 – cerebral amyloidangiopati, familjär
MeSH C18.452.648.151.175 – citrullinemi
MeSH C18.452.648.151.300 – fucosidos
MeSH C18.452.648.151.320 – galaktosemi
MeSH C18.452.648.151.330 – glykogenlagringssjukdom typ II
MeSH C18.452.648.151.355 – hartnup sjukdom
MeSH C18.452.648.151.360 – hepatolentikulär degeneration
MeSH C18.452.648.151.365 – homocystinuri
MeSH C18.452.648.151.370 – hyperargininemi
MeSH C18.452.648.151.375 – hyperglycinemi, icke-ketotisk
MeSH C18.452.648.151.380 – hyperlysinemier
MeSH C18.452.648.151.412 – Leighs sjukdom
MeSH C18.452.648.151.425 – Lesch–Nyhans syndrom
MeSH C18.452.648.151.435 – lysosomala lagringssjukdomar, nervsystemet
MeSH C18.452.648.151.435.295 – fucosidos
MeSH C18.452.648.151.435.340 – glykogenlagringssjukdom typ II
MeSH C18.452.648.151.435.590 – mukolipidoser
MeSH C18.452.648.151.435.810 – sialinsyralagringssjukdom
MeSH C18.452.648.151.435.825 – sfingolipidoser
MeSH C18.452.648.151.435.825.200 – Fabrys sjukdom
MeSH C18.452.648.151.435.825.300 – gangliosidoser
MeSH C18.452.648.151.435.825.300.300 – gangliosidoser GM2
MeSH C18.452.648.151.435.825.300.300.800 – Sandhoffs sjukdom
MeSH C18.452.648.151.435.825.300.300.840 – Tay–Sachs sjukdom
MeSH C18.452.648.151.435.825.300.300.920 – Tay–Sachs sjukdom, AB-variant
MeSH C18.452.648.151.435.825.300.400 – gangliosidos gm1
MeSH C18.452.648.151.435.825.400 – Gauchers sjukdom
MeSH C18.452.648.151.435.825.590 – leukodystrofi, globoid cell
MeSH C18.452.648.151.435.825.594 – leukodystrofi, metakromatisk
MeSH C18.452.648.151.435.825.700 – Niemann–Pick sjukdomar
MeSH C18.452.648.151.445 – lönnsirapsurinsjukdom
MeSH C18.452.648.151.447 – MELAS syndrom
MeSH C18.452.648.151.450 – menkes kinky hair syndrome
MeSH C18.452.648.151.505 – MERRF-syndrom
MeSH C18.452.648.151.580 – mukolipidoser
MeSH C18.452.648.151.640 – oculocerebrorenalt syndrom
MeSH C18.452.648.151.650 – ornitinkarbamoyltransferasbristsjukdom
MeSH C18.452.648.151.680 – peroxisomala störningar
MeSH C18.452.648.151.680.100 – adrenoleukodystrofi
MeSH C18.452.648.151.680.760 – refsum sjukdom
MeSH C18.452.648.151.680.970 – Zellwegers syndrom
MeSH C18.452.648.151.687 – fenylketonuri
MeSH C18.452.648.151.687.500 – fenylketonuri, modern
MeSH C18.452.648.151.725 – pyruvatkarboxylasbristsjukdom
MeSH C18.452.648.151.750 – pyruvatdehydrogenaskomplexbristsjukdom
MeSH C18.452.648.151.825 – sfingolipidoser
MeSH C18.452.648.151.825.200 – Fabrys sjukdom
MeSH C18.452.648.151.825.300 – gangliosidoser
MeSH C18.452.648.151.825.300.300 – gangliosidoser gm2
MeSH C18.452.648.151.825.300.300.700 – Sandhoffs sjukdom
MeSH C18.452.648.151.825.300.300.850 – Tay–Sachs sjukdom
MeSH C18.452.648.151.825.300.300.925 – Tay–Sachs sjukdom, AB-variant
MeSH C18.452.648.151.825.300.400 – gangliosidos gm1
MeSH C18.452.648.151.825.400 – Gauchers sjukdom
MeSH C18.452.648.151.825.590 – leukodystrofi, globoid cell
MeSH C18.452.648.151.825.594 – leukodystrofi, metakromatisk
MeSH C18.452.648.151.825.700 – Niemann–Pick sjukdomar
MeSH C18.452.648.151.875 – tyrosinemier
MeSH C18.452.648.202 – kolhydratmetabolism, medfödda fel
MeSH C18.452.648.202.125 – kolhydratbrist glykoproteinsyndrom
MeSH C18.452.648.202.251 – fruktosmetabolism, medfödda fel
MeSH C18.452.648.202.251.221 – fruktos-1,6-difosfatasbrist
MeSH C18.452.648.202.251.271 – Ärftlig fruktosintolerans
MeSH C18.452.648.202.303 – fucosidos
MeSH C18.452.648.202.355 – galaktosemi
MeSH C18.452.648.202.449 – glykogenlagringssjukdom
MeSH C18.452.648.202.449.448 – glykogenlagringssjukdom typ I
MeSH C18.452.648.202.449.500 – glykogenlagringssjukdom typ II
MeSH C18.452.648.202.449.510 – glykogenlagringssjukdom typ IIb
MeSH C18.452.648.202.449.520 – glykogenlagringssjukdom typ III
MeSH C18.452.648.202.449.540 – glykogenlagringssjukdom typ IV
MeSH C18.452.648.202.449.560 – glykogenlagringssjukdom typ V
MeSH C18.452.648.202.449.580 – glykogenlagringssjukdom typ VI
MeSH C18.452.648.202.449.600 – glykogenlagringssjukdom typ VII
MeSH C18.452.648.202.449.620 – glykogenlagringssjukdom typ VIII
MeSH C18.452.648.202.460 – hyperoxaluri, primär
MeSH C18.452.648.202.589 – laktosintolerans
MeSH C18.452.648.202.607 – sjukdomar med mannosidasbrist
MeSH C18.452.648.202.607.500 – alfa-mannosidos
MeSH C18.452.648.202.607.750 – beta-mannosidos
MeSH C18.452.648.202.670 – mukolipidoser
MeSH C18.452.648.202.715 – mukopolysackaridoser
MeSH C18.452.648.202.715.640 – mukopolysackaridos I
MeSH C18.452.648.202.715.645 – mukopolysackaridos II
MeSH C18.452.648.202.715.650 – mukopolysackaridos III
MeSH C18.452.648.202.715.655 – mukopolysackaridos IV
MeSH C18.452.648.202.715.670 – mukopolysackaridos VI
MeSH C18.452.648.202.715.675 – mukopolysackaridos VII
MeSH C18.452.648.202.720 – multipel karboxylasbrist
MeSH C18.452.648.202.720.100 – biotinidasbrist
MeSH C18.452.648.202.720.380 – holokarboxylassyntetasbrist
MeSH C18.452.648.202.810 – pyruvatmetabolism, medfödda fel
MeSH C18.452.648.202.810.444 – Leigh disease
MeSH C18.452.648.202.810.666 – pyruvatkarboxylasbristsjukdom
MeSH C18.452.648.202.810.766 – pyruvatdehydrogenaskomplexbristsjukdom
MeSH C18.452.648.240 – brist på cytokrom-c-oxidas
MeSH C18.452.648.390 – glukosfosfatdehydrogenasbrist
MeSH C18.452.648.437 – hyperbilirubinemi, ärftlig
MeSH C18.452.648.437.281 – Crigler–Najjars syndrom
MeSH C18.452.648.437.528 – Gilberts sjukdom
MeSH C18.452.648.499 – gulsot, kronisk idiopatisk
MeSH C18.452.648.556 – lipidmetabolism, medfödda fel
MeSH C18.452.648.556.475 – hyperkolesterolemi, familjär
MeSH C18.452.648.556.480 – hyperlipidemi, familjär kombinerad
MeSH C18.452.648.556.480.390 – hyperkolesterolemi, familjär
MeSH C18.452.648.556.480.395 – hyperlipoproteinemi typ IV
MeSH C18.452.648.556.484 – hyperlipoproteinemi typ III
MeSH C18.452.648.556.490 – hyperlipoproteinemi typ IV
MeSH C18.452.648.556.495 – hyperlipoproteinemi typ V
MeSH C18.452.648.556.500 – hypolipoproteinemi
MeSH C18.452.648.556.500.220 – abetalipoproteinemi
MeSH C18.452.648.556.500.440 – hypobetalipoproteinemi
MeSH C18.452.648.556.500.448 – lecitinacyltransferasbrist
MeSH C18.452.648.556.500.724 – Tangers sjukdom
MeSH C18.452.648.556.641 – lipoidos
MeSH C18.452.648.556.641.201 – kolesterolesterlagringssjukdom
MeSH C18.452.648.556.641.391 – lipoidproteinos
MeSH C18.452.648.556.641.509 – neuronal ceroid lipofuscinosis
MeSH C18.452.648.556.641.643 – Refsums sjukdom
MeSH C18.452.648.556.641.723 – Sjögren–Larssons syndrom
MeSH C18.452.648.556.641.803 – sfingolipidoser
MeSH C18.452.648.556.641.803.300 – Fabrys sjukdom
MeSH C18.452.648.556.641.803.350 – gangliosidoser
MeSH C18.452.648.556.641.803.350.300 – gangliosidoser GM2
MeSH C18.452.648.556.641.803.350.300.700 – Sandhoffs sjukdom
MeSH C18.452.648.556.641.803.350.300.850 – Tay–Sachs sjukdom
MeSH C18.452.648.556.641.803.350.300.925 – Tay–Sachs sjukdom, AB-variant
MeSH C18.452.648.556.641.803.350.360 – gangliosidos gm1
MeSH C18.452.648.556.641.803.441 – Gauchers sjukdom
MeSH C18.452.648.556.641.803.585 – leukodystrofi, globoid cell
MeSH C18.452.648.556.641.803.594 – leukodystrofi, metakromatisk
MeSH C18.452.648.556.641.803.730 – Niemann–Pick sjukdomar
MeSH C18.452.648.556.641.803.850 – havsblått histiocytsyndrom
MeSH C18.452.648.556.641.923 – Wolmans sjukdom
MeSH C18.452.648.556.645 – lipoproteinlipasbrist, familjär
MeSH C18.452.648.556.750 – peroxisomala störningar
MeSH C18.452.648.556.750.025 – acatalasia
MeSH C18.452.648.556.750.112 – adrenoleukodystrofi
MeSH C18.452.648.556.750.200 – chondrodysplasia punctata, rhizomelic
MeSH C18.452.648.556.750.760 – Refsum sjukdom
MeSH C18.452.648.556.750.970 – Zellwegers syndrom
MeSH C18.452.648.556.850 – Smith–Lemli–Opitz syndrom
MeSH C18.452.648.556.925 – xantomatos, cerebrotendinös
MeSH C18.452.648.595 – lysosomala lagringssjukdomar
MeSH C18.452.648.595.201 – kolesterolesterlagringssjukdom
MeSH C18.452.648.595.554 – lysosomala lagringssjukdomar, nervsystemet
MeSH C18.452.648.595.554.295 – fucosidos
MeSH C18.452.648.595.554.340 – glykogenlagringssjukdom typ II
MeSH C18.452.648.595.554.590 – mukolipidoser
MeSH C18.452.648.595.554.810 – sialinsyralagringssjukdom
MeSH C18.452.648.595.554.825 – sfingolipidoser
MeSH C18.452.648.595.554.825.200 – Fabrys sjukdom
MeSH C18.452.648.595.554.825.300 – gangliosidoser
MeSH C18.452.648.595.554.825.300.300 – gangliosidoser GM2
MeSH C18.452.648.595.554.825.300.300.800 – Sandhoffs sjukdom
MeSH C18.452.648.595.554.825.300.300.840 – Tay–Sachs sjukdom
MeSH C18.452.648.595.554.825.300.300.920 – Tay–Sachs sjukdom, AB-variant
MeSH C18.452.648.595.554.825.300.400 – gangliosidos gm1
MeSH C18.452.648.595.554.825.400 – Gauchers sjukdom
MeSH C18.452.648.595.554.825.590 – leukodystrofi, globoidcell
MeSH C18.452.648.595.554.825.594 – leukodystrofi, metakromatisk
MeSH C18.452.648.595.554.825.700 – Niemann–Pick sjukdomar
MeSH C18.452.648.595.577 – sjukdomar med mannosidasbrist
MeSH C18.452.648.595.577.500 – alfa-mannosidos
MeSH C18.452.648.595.577.750 – beta-mannosidos
MeSH C18.452.648.595.600 – mukopolysackaridoser
MeSH C18.452.648.595.600.640 – mukopolysackaridos I
MeSH C18.452.648.595.600.645 – mukopolysackaridos II
MeSH C18.452.648.595.600.650 – mukopolysackaridos III
MeSH C18.452.648.595.600.655 – mukopolysackaridos IV
MeSH C18.452.648.595.600.670 – mukopolysackaridos VI
MeSH C18.452.648.595.600.675 – mukopolysackaridos VII
MeSH C18.452.648.595.803 – sfingolipidoser
MeSH C18.452.648.595.803.300 – Fabrys sjukdom
MeSH C18.452.648.595.803.350 – gangliosidoser
MeSH C18.452.648.595.803.350.300 – gangliosidoser GM2
MeSH C18.452.648.595.803.350.300.700 – Sandhoffs sjukdom
MeSH C18.452.648.595.803.350.300.850 – Tay–Sachs sjukdom
MeSH C18.452.648.595.803.350.300.925 – Tay–Sachs sjukdom, AB-variant
MeSH C18.452.648.595.803.441 – Gauchers sjukdom
MeSH C18.452.648.595.803.585 – leukodystrofi, globoid cell
MeSH C18.452.648.595.803.594 – leukodystrofi, metakromatisk
MeSH C18.452.648.595.803.730 – Niemann–Pick sjukdomar
MeSH C18.452.648.595.803.850 – havsblått histiocytsyndrom
MeSH C18.452.648.595.923 – Wolmans sjukdom
MeSH C18.452.648.618 – metallmetabolism, medfödda fel
MeSH C18.452.648.618.337 – hemokromatos
MeSH C18.452.648.618.403 – hepatolentikulär degeneration
MeSH C18.452.648.618.482 – hypofosfatasi
MeSH C18.452.648.618.544 – hypofosfatemi, familjär
MeSH C18.452.648.618.590 – Menkes kinky hair syndrome
MeSH C18.452.648.618.711 – förlamningar, familjär periodisk
MeSH C18.452.648.618.711.550 – hypokalemisk periodisk förlamning
MeSH C18.452.648.618.711.600 – förlamning, hyperkalemisk periodisk
MeSH C18.452.648.618.815 – pseudohypoparatyreos
MeSH C18.452.648.618.815.815 – pseudopseudohypoparatyreoidism
MeSH C18.452.648.730 – porfyri, erytropoetisk
MeSH C18.452.648.735 – porfyri, lever
MeSH C18.452.648.735.074 – koproporfyri, ärftlig
MeSH C18.452.648.735.150 – porfyri, akut intermittent
MeSH C18.452.648.735.250 – porphyria cutanea tarda
MeSH C18.452.648.735.437 – porfyri, hepatoerytropoetisk
MeSH C18.452.648.735.625 – porfyri, variegate
MeSH C18.452.648.735.812 – protoporfyri, erytropoetisk
MeSH C18.452.648.769 – progeria
MeSH C18.452.648.798 – purin–pyrimidinmetabolism, medfödda fel
MeSH C18.452.648.798.368 – gikt
MeSH C18.452.648.798.368.410 – artrit, gikt
MeSH C18.452.648.798.594 – Lesch–Nyhans syndrom
MeSH C18.452.648.851 – njurrörstransport, medfödda fel
MeSH C18.452.648.851.093 – acidos, renal tubulär
MeSH C18.452.648.851.191 – aminoaciduri, renal
MeSH C18.452.648.851.191.250 – cystinuri
MeSH C18.452.648.851.191.457 – Hartnups sjukdom
MeSH C18.452.648.851.368 – cystinos
MeSH C18.452.648.851.368.210 – Fanconis syndrom
MeSH C18.452.648.851.532 – glykosuri, njure
MeSH C18.452.648.851.647 – hypofosfatemi, familjär
MeSH C18.452.648.851.750 – oculocerebrorenalt syndrom
MeSH C18.452.648.851.770 – pseudohypoaldosteronism
MeSH C18.452.648.925 – steroidmetabolism, medfödda fel
MeSH C18.452.648.925.249 – binjurehyperplasi, medfödd
MeSH C18.452.648.925.500 – mineralokortikoid överskottssyndrom, uppenbart
MeSH C18.452.648.925.750 – iktyos, x-länkad
MeSH C18.452.648.925.875 – Smith–Lemli–Opitz syndrom

MeSH C18.452.660 – mitokondriella sjukdomar

MeSH C18.452.660.195 – cytokrom-c-oxidasbrist
MeSH C18.452.660.300 – Friedreichs ataxi
MeSH C18.452.660.515 – optisk atrofi, ärftlig, leber
MeSH C18.452.660.520 – Leigh sjukdom
MeSH C18.452.660.560 – mitokondriella myopatier
MeSH C18.452.660.560.620 – mitokondriella encefalomyopatier
MeSH C18.452.660.560.620.520 – MELAS syndrom
MeSH C18.452.660.560.620.530 – MERRF-syndrom
MeSH C18.452.660.560.700 – oftalmoplegi, kronisk progressiv extern
MeSH C18.452.660.560.700.500 – Kearns–Sayre syndrom
MeSH C18.452.660.665 – optisk atrofi, autosomal dominant
MeSH C18.452.660.705 – pyruvatkarboxylasbristsjukdom
MeSH C18.452.660.710 – pyruvatdehydrogenaskomplexbristsjukdom

MeSH C18.452.730 – ochronosis

MeSH C18.452.750 – störningar i fosformetabolismen

MeSH C18.452.750.400 – hypofosfatemi

MeSH C18.452.872 – hudsjukdomar, metabola

MeSH C18.452.872.077 – adiposis dolorosa
MeSH C18.452.872.617 – porfyri
MeSH C18.452.872.617.250 – porfyri, erytropoetisk
MeSH C18.452.872.617.400 – porfyri, lever
MeSH C18.452.872.617.400.074 – koproporfyri, ärftlig
MeSH C18.452.872.617.400.150 – porfyri, akut intermittent
MeSH C18.452.872.617.400.250 – porphyria cutanea tarda
MeSH C18.452.872.617.400.437 – porfyri, hepatoerytropoetisk
MeSH C18.452.872.617.400.625 – porfyri, variegate
MeSH C18.452.872.617.400.812 – protoporfyri, erytropoetisk
MeSH C18.452.872.866 – xanthogranulom, juvenil
MeSH C18.452.872.929 – xantomatos
MeSH C18.452.872.929.950 – wolman sjukdom
MeSH C18.452.872.929.975 – xantomatos, cerebrotendinös

MeSH C18.452.940 – wasting syndrome

MeSH C18.452.940.520 – hiv wasting syndrome

MeSH C18.452.950 – vatten-elektrolyt-obalans

MeSH C18.452.950.179 – uttorkning
MeSH C18.452.950.340 – hyperkalcemi
MeSH C18.452.950.396 – hyperkalemi
MeSH C18.452.950.452 – hypernatremi
MeSH C18.452.950.509 – hypokalcemi
MeSH C18.452.950.565 – hypokalemi
MeSH C18.452.950.620 – hyponatremi
MeSH C18.452.950.626 – olämpligt adh-syndrom
MeSH C18.452.950.932 – vattenförgiftning

MeSH C18.654 – nutritionsstörningar

MeSH C18.654.180 – barnnäringsstörningar

MeSH C18.654.422 – spädbarnsnäringsstörningar

MeSH C18.654.422.360 – hemorragisk sjukdom hos nyfödda

MeSH C18.654.521 – undernäring

MeSH C18.654.521.500 – bristsjukdomar
MeSH C18.654.521.500.133 – avitaminos
MeSH C18.654.521.500.133.115 – askorbinsyrabrist
MeSH C18.654.521.500.133.115.661 – skörbjugg
MeSH C18.654.521.500.133.628 – A-vitaminbrist
MeSH C18.654.521.500.133.699 – vitamin B-brist
MeSH C18.654.521.500.133.699.160 – kolinbrist
MeSH C18.654.521.500.133.699.308 – folsyrabrist
MeSH C18.654.521.500.133.699.529 – pellagra
MeSH C18.654.521.500.133.699.713 – riboflavinbrist
MeSH C18.654.521.500.133.699.827 – tiaminbrist
MeSH C18.654.521.500.133.699.827.223 – beriberi
MeSH C18.654.521.500.133.699.827.822 – wernicke encefalopati
MeSH C18.654.521.500.133.699.901 – vitamin B6-brist
MeSH C18.654.521.500.133.699.923 – vitamin B12-brist
MeSH C18.654.521.500.133.699.923.280 – anemi, perniciös
MeSH C18.654.521.500.133.770 – D-vitaminbrist
MeSH C18.654.521.500.133.770.496 – osteomalaci
MeSH C18.654.521.500.133.770.734 – rakitis
MeSH C18.654.521.500.133.841 – E-vitaminbrist
MeSH C18.654.521.500.133.841.682 – steatit
MeSH C18.654.521.500.133.912 – vitamin K-brist
MeSH C18.654.521.500.133.912.360 – hemorragisk sjukdom hos nyfödda
MeSH C18.654.521.500.439 – magnesiumbrist
MeSH C18.654.521.500.617 – kaliumbrist
MeSH C18.654.521.500.708 – proteinbrist
MeSH C18.654.521.500.708.626 – protein-energi undernäring
MeSH C18.654.521.500.708.626.505 – kwashiorkor
MeSH C18.654.521.500.857 – swayback
MeSH C18.654.521.625 – fostrets nutritionsstörningar
MeSH C18.654.521.750 – svält

MeSH C18.654.726 – övernäring

MeSH C18.654.726.500 – fetma
MeSH C18.654.726.500.695 – fetma hypoventilationssyndrom
MeSH C18.654.726.500.700 – fetma, sjuklig
MeSH C18.654.726.500.740 – Prader–Willis syndrom

MeSH C18.654.940 – wasting syndrome

MeSH C18.654.940.520 – hiv wasting syndrome

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