“List of MeSH codes (C18)”的意思、由来-开放百科全书

词条

List of MeSH codes (C18)

释义

{{MeshNumber|C18|Nutritional+and+Metabolic+Diseases}} --- nutritional and metabolic diseases
{{MeshNumber|C18.452|Metabolic+Diseases}} --- metabolic diseases {{MeshNumber|C18.452.076|Acid-Base+Imbalance}} --- acid-base imbalance {{MeshNumber|C18.452.090|Amyloidosis}} --- amyloidosis {{MeshNumber|C18.452.100|Brain+Diseases,+Metabolic}} --- brain diseases, metabolic {{MeshNumber|C18.452.174|Calcium+Metabolism+Disorders}} --- calcium metabolism disorders {{MeshNumber|C18.452.284|DNA+Repair-Deficiency+Disorders}} --- dna repair-deficiency disorders {{MeshNumber|C18.452.339|Dyslipidemias}} --- dyslipidemias {{MeshNumber|C18.452.394|Glucose+Metabolism+Disorders}} --- glucose metabolism disorders {{MeshNumber|C18.452.413|Hyperammonemia}} --- hyperammonemia {{MeshNumber|C18.452.421|Hyperamylasemia}} --- hyperamylasemia {{MeshNumber|C18.452.429|Hyperbilirubinemia}} --- hyperbilirubinemia {{MeshNumber|C18.452.497|Hyperoxaluria}} --- hyperoxaluria {{MeshNumber|C18.452.500|Hyperprolactinemia}} --- hyperprolactinemia {{MeshNumber|C18.452.506|Hyperuricemia}} --- hyperuricemia {{MeshNumber|C18.452.512|Hypervitaminosis+A}} --- hypervitaminosis a {{MeshNumber|C18.452.565|Iron+Metabolism+Disorders}} --- iron metabolism disorders {{MeshNumber|C18.452.603|Malabsorption+Syndromes}} --- malabsorption syndromes {{MeshNumber|C18.452.625|Metabolic+Syndrome+X}} --- metabolic syndrome x {{MeshNumber|C18.452.648|Metabolism,+Inborn+Errors}} --- metabolism, inborn errors {{MeshNumber|C18.452.660|Mitochondrial+Diseases}} --- mitochondrial diseases {{MeshNumber|C18.452.730|Ochronosis}} --- ochronosis {{MeshNumber|C18.452.750|Phosphorus+Metabolism+Disorders}} --- phosphorus metabolism disorders {{MeshNumber|C18.452.872|Skin+Diseases,+Metabolic}} --- skin diseases, metabolic {{MeshNumber|C18.452.940|Wasting+Syndrome}} --- wasting syndrome {{MeshNumber|C18.452.950|Water-Electrolyte+Imbalance}} --- water-electrolyte imbalance {{MeshNumber|C18.654|Nutrition+Disorders}} --- nutrition disorders {{MeshNumber|C18.654.180|Child+Nutrition+Disorders}} --- child nutrition disorders {{MeshNumber|C18.654.422|Infant+Nutrition+Disorders}} --- infant nutrition disorders {{MeshNumber|C18.654.521|Malnutrition}} --- malnutrition {{MeshNumber|C18.654.726|Overnutrition}} --- overnutrition {{MeshNumber|C18.654.940|Wasting+Syndrome}} --- wasting syndrome

The following is a list of the "C" codes for MeSH. It is a product of the United States National Library of Medicine.

Source for content is [https://www.nlm.nih.gov/mesh/filelist.html here]. (File "2006 MeSH Trees".)

{{MeshNumber|C18|Nutritional+and+Metabolic+Diseases}} --- nutritional and metabolic diseases

{{MeshNumber|C18.452|Metabolic+Diseases}} --- metabolic diseases

{{MeshNumber|C18.452.076|Acid-Base+Imbalance}} --- acid-base imbalance

{{MeshNumber|C18.452.076.087|Achlorhydria}} --- achlorhydria
{{MeshNumber|C18.452.076.176|Acidosis}} --- acidosis
{{MeshNumber|C18.452.076.176.180|Acidosis,+Lactic}} --- acidosis, lactic
{{MeshNumber|C18.452.076.176.210|Acidosis,+Renal+Tubular}} --- acidosis, renal tubular
{{MeshNumber|C18.452.076.176.310|Acidosis,+Respiratory}} --- acidosis, respiratory
{{MeshNumber|C18.452.076.176.390|Diabetic+Ketoacidosis}} --- diabetic ketoacidosis
{{MeshNumber|C18.452.076.176.652|Ketosis}} --- ketosis
{{MeshNumber|C18.452.076.354|Alkalosis}} --- alkalosis
{{MeshNumber|C18.452.076.354.271|Alkalosis,+Respiratory}} --- alkalosis, respiratory

{{MeshNumber|C18.452.090|Amyloidosis}} --- amyloidosis

{{MeshNumber|C18.452.090.050|Amyloid+Neuropathies}} --- amyloid neuropathies
{{MeshNumber|C18.452.090.050.050|Amyloid+Neuropathies,+Familial}} --- amyloid neuropathies, familial
{{MeshNumber|C18.452.090.075|Amyloidosis,+Familial}} --- amyloidosis, familial
{{MeshNumber|C18.452.090.075.050|Amyloid+Neuropathies,+Familial}} --- amyloid neuropathies, familial
{{MeshNumber|C18.452.090.075.160|Cerebral+Amyloid+Angiopathy,+Familial}} --- cerebral amyloid angiopathy, familial
{{MeshNumber|C18.452.090.100|Cerebral+Amyloid+Angiopathy}} --- cerebral amyloid angiopathy
{{MeshNumber|C18.452.090.100.160|Cerebral+Amyloid+Angiopathy,+Familial}} --- cerebral amyloid angiopathy, familial

{{MeshNumber|C18.452.100|Brain+Diseases,+Metabolic}} --- brain diseases, metabolic

{{MeshNumber|C18.452.100.100|Brain+Diseases,+Metabolic,+Inborn}} --- brain diseases, metabolic, inborn
{{MeshNumber|C18.452.100.100.050|Abetalipoproteinemia}} --- abetalipoproteinemia
{{MeshNumber|C18.452.100.100.162|Carbamoyl-Phosphate+Synthase+I+Deficiency+Disease}} --- carbamoyl-phosphate synthase i deficiency disease
{{MeshNumber|C18.452.100.100.175|Citrullinemia}} --- citrullinemia
{{MeshNumber|C18.452.100.100.320|Galactosemias}} --- galactosemias
{{MeshNumber|C18.452.100.100.355|Hartnup+Disease}} --- hartnup disease
{{MeshNumber|C18.452.100.100.360|Hepatolenticular+Degeneration}} --- hepatolenticular degeneration
{{MeshNumber|C18.452.100.100.365|Homocystinuria}} --- homocystinuria
{{MeshNumber|C18.452.100.100.370|Hyperargininemia}} --- hyperargininemia
{{MeshNumber|C18.452.100.100.375|Hyperglycinemia,+Nonketotic}} --- hyperglycinemia, nonketotic
{{MeshNumber|C18.452.100.100.380|Hyperlysinemias}} --- hyperlysinemias
{{MeshNumber|C18.452.100.100.412|Leigh+Disease}} --- leigh disease
{{MeshNumber|C18.452.100.100.425|Lesch-Nyhan+Syndrome}} --- lesch-nyhan syndrome
{{MeshNumber|C18.452.100.100.435|Lysosomal+Storage+Diseases,+Nervous+System}} --- lysosomal storage diseases, nervous system
{{MeshNumber|C18.452.100.100.435.295|Fucosidosis}} --- fucosidosis
{{MeshNumber|C18.452.100.100.435.340|Glycogen+Storage+Disease+Type+II}} --- glycogen storage disease type ii
{{MeshNumber|C18.452.100.100.435.590|Mucolipidoses}} --- mucolipidoses
{{MeshNumber|C18.452.100.100.435.810|Sialic+Acid+Storage+Disease}} --- sialic acid storage disease
{{MeshNumber|C18.452.100.100.435.825|Sphingolipidoses}} --- sphingolipidoses
{{MeshNumber|C18.452.100.100.435.825.200|Fabry+Disease}} --- fabry disease
{{MeshNumber|C18.452.100.100.435.825.300|Gangliosidoses}} --- gangliosidoses
{{MeshNumber|C18.452.100.100.435.825.300.300|Gangliosidoses+GM2}} --- gangliosidoses gm2
{{MeshNumber|C18.452.100.100.435.825.300.300.800|Sandhoff+Disease}} --- sandhoff disease
{{MeshNumber|C18.452.100.100.435.825.300.300.840|Tay-Sachs+Disease}} --- tay-sachs disease
{{MeshNumber|C18.452.100.100.435.825.300.300.920|Tay-Sachs+Disease,+AB+Variant}} --- tay-sachs disease, ab variant
{{MeshNumber|C18.452.100.100.435.825.300.400|Gangliosidosis+GM1}} --- gangliosidosis gm1
{{MeshNumber|C18.452.100.100.435.825.400|Gaucher+Disease}} --- gaucher disease
{{MeshNumber|C18.452.100.100.435.825.590|Leukodystrophy,+Globoid+Cell}} --- leukodystrophy, globoid cell
{{MeshNumber|C18.452.100.100.435.825.594|Leukodystrophy,+Metachromatic}} --- leukodystrophy, metachromatic
{{MeshNumber|C18.452.100.100.435.825.700|Niemann-Pick+Diseases}} --- niemann-pick diseases
{{MeshNumber|C18.452.100.100.520|Maple+Syrup+Urine+Disease}} --- maple syrup urine disease
{{MeshNumber|C18.452.100.100.535|MELAS+Syndrome}} --- melas syndrome
{{MeshNumber|C18.452.100.100.540|Menkes+Kinky+Hair+Syndrome}} --- menkes kinky hair syndrome
{{MeshNumber|C18.452.100.100.545|MERRF+Syndrome}} --- merrf syndrome
{{MeshNumber|C18.452.100.100.640|Oculocerebrorenal+Syndrome}} --- oculocerebrorenal syndrome
{{MeshNumber|C18.452.100.100.650|Ornithine+Carbamoyltransferase+Deficiency+Disease}} --- ornithine carbamoyltransferase deficiency disease
{{MeshNumber|C18.452.100.100.680|Peroxisomal+Disorders}} --- peroxisomal disorders
{{MeshNumber|C18.452.100.100.680.100|Adrenoleukodystrophy}} --- adrenoleukodystrophy
{{MeshNumber|C18.452.100.100.680.760|Refsum+Disease}} --- refsum disease
{{MeshNumber|C18.452.100.100.680.970|Zellweger+Syndrome}} --- zellweger syndrome
{{MeshNumber|C18.452.100.100.687|Phenylketonurias}} --- phenylketonurias
{{MeshNumber|C18.452.100.100.687.500|Phenylketonuria,+Maternal}} --- phenylketonuria, maternal
{{MeshNumber|C18.452.100.100.725|Pyruvate+Carboxylase+Deficiency+Disease}} --- pyruvate carboxylase deficiency disease
{{MeshNumber|C18.452.100.100.750|Pyruvate+Dehydrogenase+Complex+Deficiency+Disease}} --- pyruvate dehydrogenase complex deficiency disease
{{MeshNumber|C18.452.100.100.875|Tyrosinemias}} --- tyrosinemias
{{MeshNumber|C18.452.100.360|Hepatic+Encephalopathy}} --- hepatic encephalopathy
{{MeshNumber|C18.452.100.480|Kernicterus}} --- kernicterus
{{MeshNumber|C18.452.100.540|Mitochondrial+Encephalomyopathies}} --- mitochondrial encephalomyopathies
{{MeshNumber|C18.452.100.560|Myelinolysis,+Central+Pontine}} --- myelinolysis, central pontine
{{MeshNumber|C18.452.100.780|Reye+Syndrome}} --- reye syndrome
{{MeshNumber|C18.452.100.960|Wernicke+Encephalopathy}} --- wernicke encephalopathy

{{MeshNumber|C18.452.174|Calcium+Metabolism+Disorders}} --- calcium metabolism disorders

{{MeshNumber|C18.452.174.130|Calcinosis}} --- calcinosis
{{MeshNumber|C18.452.174.130.186|Calciphylaxis}} --- calciphylaxis
{{MeshNumber|C18.452.174.130.204|CREST+Syndrome}} --- crest syndrome
{{MeshNumber|C18.452.174.130.560|Nephrocalcinosis}} --- nephrocalcinosis
{{MeshNumber|C18.452.174.289|Decalcification,+Pathologic}} --- decalcification, pathologic
{{MeshNumber|C18.452.174.451|Hypercalcemia}} --- hypercalcemia
{{MeshNumber|C18.452.174.509|Hypocalcemia}} --- hypocalcemia
{{MeshNumber|C18.452.174.509.700|Tetany}} --- tetany
{{MeshNumber|C18.452.174.662|Osteomalacia}} --- osteomalacia
{{MeshNumber|C18.452.174.766|Pseudohypoparathyroidism}} --- pseudohypoparathyroidism
{{MeshNumber|C18.452.174.766.815|Pseudopseudohypoparathyroidism}} --- pseudopseudohypoparathyroidism
{{MeshNumber|C18.452.174.845|Rickets}} --- rickets

{{MeshNumber|C18.452.284|DNA+Repair-Deficiency+Disorders}} --- dna repair-deficiency disorders

{{MeshNumber|C18.452.284.060|Ataxia+Telangiectasia}} --- ataxia telangiectasia
{{MeshNumber|C18.452.284.100|Bloom+Syndrome}} --- bloom syndrome
{{MeshNumber|C18.452.284.250|Cockayne+Syndrome}} --- cockayne syndrome
{{MeshNumber|C18.452.284.255|Colorectal+Neoplasms,+Hereditary+Nonpolyposis}} --- colorectal neoplasms, hereditary nonpolyposis
{{MeshNumber|C18.452.284.280|Fanconi+Anemia}} --- fanconi anemia
{{MeshNumber|C18.452.284.520|Li-Fraumeni+Syndrome}} --- li-fraumeni syndrome
{{MeshNumber|C18.452.284.600|Nijmegen+Breakage+Syndrome}} --- nijmegen breakage syndrome
{{MeshNumber|C18.452.284.760|Rothmund-Thomson+Syndrome}} --- rothmund-thomson syndrome
{{MeshNumber|C18.452.284.800|Severe+Combined+Immunodeficiency}} --- severe combined immunodeficiency
{{MeshNumber|C18.452.284.960|Werner+Syndrome}} --- werner syndrome
{{MeshNumber|C18.452.284.975|Xeroderma+Pigmentosum}} --- xeroderma pigmentosum

{{MeshNumber|C18.452.339|Dyslipidemias}} --- dyslipidemias

{{MeshNumber|C18.452.339.500|Hyperlipidemia}} --- hyperlipidemia
{{MeshNumber|C18.452.339.500.396|Hypercholesterolemia}} --- hypercholesterolemia
{{MeshNumber|C18.452.339.500.396.300|Hypercholesterolemia,+Familial}} --- hypercholesterolemia, familial
{{MeshNumber|C18.452.339.500.438|Hyperlipidemia,+Familial+Combined}} --- hyperlipidemia, familial combined
{{MeshNumber|C18.452.339.500.438.390|Hypercholesterolemia,+Familial}} --- hypercholesterolemia, familial
{{MeshNumber|C18.452.339.500.438.395|Hyperlipoproteinemia+Type+IV}} --- hyperlipoproteinemia type iv
{{MeshNumber|C18.452.339.500.851|Hypertriglyceridemia}} --- hypertriglyceridemia
{{MeshNumber|C18.452.339.750|Hyperlipoproteinemia}} --- hyperlipoproteinemia
{{MeshNumber|C18.452.339.750.475|Hypercholesterolemia,+Familial}} --- hypercholesterolemia, familial
{{MeshNumber|C18.452.339.750.485|Hyperlipoproteinemia+Type+III}} --- hyperlipoproteinemia type iii
{{MeshNumber|C18.452.339.750.490|Hyperlipoproteinemia+Type+IV}} --- hyperlipoproteinemia type iv
{{MeshNumber|C18.452.339.750.495|Hyperlipoproteinemia+Type+V}} --- hyperlipoproteinemia type v
{{MeshNumber|C18.452.339.750.552|Lipoprotein+Lipase+Deficiency,+Familial}} --- lipoprotein lipase deficiency, familial
{{MeshNumber|C18.452.339.875|Hypolipoproteinemia}} --- hypolipoproteinemia
{{MeshNumber|C18.452.339.875.220|Abetalipoproteinemia}} --- abetalipoproteinemia
{{MeshNumber|C18.452.339.875.440|Hypobetalipoproteinemia}} --- hypobetalipoproteinemia
{{MeshNumber|C18.452.339.875.448|Lecithin+Acyltransferase+Deficiency}} --- lecithin acyltransferase deficiency
{{MeshNumber|C18.452.339.875.724|Tangier+Disease}} --- tangier disease

{{MeshNumber|C18.452.394|Glucose+Metabolism+Disorders}} --- glucose metabolism disorders

{{MeshNumber|C18.452.394.750|Diabetes+Mellitus}} --- diabetes mellitus
{{MeshNumber|C18.452.394.750.074|Diabetes+Mellitus,+Experimental}} --- diabetes mellitus, experimental
{{MeshNumber|C18.452.394.750.124|Diabetes+Mellitus,+Type+1}} --- diabetes mellitus, type 1
{{MeshNumber|C18.452.394.750.124.960|Wolfram+Syndrome}} --- wolfram syndrome
{{MeshNumber|C18.452.394.750.149|Diabetes+Mellitus,+Type+2}} --- diabetes mellitus, type 2
{{MeshNumber|C18.452.394.750.149.500|Diabetes+Mellitus,+Lipoatrophic}} --- diabetes mellitus, lipoatrophic
{{MeshNumber|C18.452.394.750.448|Diabetes,+Gestational}} --- diabetes, gestational
{{MeshNumber|C18.452.394.750.535|Diabetic+Ketoacidosis}} --- diabetic ketoacidosis
{{MeshNumber|C18.452.394.750.774|Prediabetic+State}} --- prediabetic state
{{MeshNumber|C18.452.394.937|Glycosuria}} --- glycosuria
{{MeshNumber|C18.452.394.937.450|Glycosuria,+Renal}} --- glycosuria, renal
{{MeshNumber|C18.452.394.952|Hyperglycemia}} --- hyperglycemia
{{MeshNumber|C18.452.394.952.500|Glucose+Intolerance}} --- glucose intolerance
{{MeshNumber|C18.452.394.968|Hyperinsulinism}} --- hyperinsulinism
{{MeshNumber|C18.452.394.968.500|Insulin+Resistance}} --- insulin resistance
{{MeshNumber|C18.452.394.968.500.570|Metabolic+Syndrome+X}} --- metabolic syndrome x
{{MeshNumber|C18.452.394.968.750|Persistent+Hyperinsulinemia+Hypoglycemia+of+Infancy}} --- persistent hyperinsulinemia hypoglycemia of infancy
{{MeshNumber|C18.452.394.984|Hypoglycemia}} --- hypoglycemia
{{MeshNumber|C18.452.394.984.492|Insulin+Coma}} --- insulin coma
{{MeshNumber|C18.452.394.984.746|Persistent+Hyperinsulinemia+Hypoglycemia+of+Infancy}} --- persistent hyperinsulinemia hypoglycemia of infancy

{{MeshNumber|C18.452.413|Hyperammonemia}} --- hyperammonemia

{{MeshNumber|C18.452.421|Hyperamylasemia}} --- hyperamylasemia

{{MeshNumber|C18.452.429|Hyperbilirubinemia}} --- hyperbilirubinemia

{{MeshNumber|C18.452.429.124|Hyperbilirubinemia,+Neonatal}} --- hyperbilirubinemia, neonatal
{{MeshNumber|C18.452.429.124.500|Jaundice,+Neonatal}} --- jaundice, neonatal
{{MeshNumber|C18.452.429.500|Kernicterus}} --- kernicterus

{{MeshNumber|C18.452.497|Hyperoxaluria}} --- hyperoxaluria

{{MeshNumber|C18.452.497.490|Hyperoxaluria,+Primary}} --- hyperoxaluria, primary

{{MeshNumber|C18.452.500|Hyperprolactinemia}} --- hyperprolactinemia

{{MeshNumber|C18.452.506|Hyperuricemia}} --- hyperuricemia

{{MeshNumber|C18.452.512|Hypervitaminosis+A}} --- hypervitaminosis a

{{MeshNumber|C18.452.565|Iron+Metabolism+Disorders}} --- iron metabolism disorders

{{MeshNumber|C18.452.565.100|Anemia,+Iron-Deficiency}} --- anemia, iron-deficiency
{{MeshNumber|C18.452.565.500|Iron+Overload}} --- iron overload
{{MeshNumber|C18.452.565.500.480|Hemochromatosis}} --- hemochromatosis
{{MeshNumber|C18.452.565.500.500|Hemosiderosis}} --- hemosiderosis

{{MeshNumber|C18.452.603|Malabsorption+Syndromes}} --- malabsorption syndromes

{{MeshNumber|C18.452.603.145|Blind+Loop+Syndrome}} --- blind loop syndrome
{{MeshNumber|C18.452.603.250|Celiac+Disease}} --- celiac disease
{{MeshNumber|C18.452.603.506|Lactose+Intolerance}} --- lactose intolerance
{{MeshNumber|C18.452.603.850|Sprue,+Tropical}} --- sprue, tropical
{{MeshNumber|C18.452.603.887|Steatorrhea}} --- steatorrhea
{{MeshNumber|C18.452.603.925|Whipple+Disease}} --- whipple disease

{{MeshNumber|C18.452.625|Metabolic+Syndrome+X}} --- metabolic syndrome x

{{MeshNumber|C18.452.648|Metabolism,+Inborn+Errors}} --- metabolism, inborn errors

{{MeshNumber|C18.452.648.066|Amino+Acid+Metabolism,+Inborn+Errors}} --- amino acid metabolism, inborn errors
{{MeshNumber|C18.452.648.066.102|Albinism}} --- albinism
{{MeshNumber|C18.452.648.066.102.090|Albinism,+Ocular}} --- albinism, ocular
{{MeshNumber|C18.452.648.066.102.100|Albinism,+Oculocutaneous}} --- albinism, oculocutaneous
{{MeshNumber|C18.452.648.066.102.100.400|Hermanski-Pudlak+Syndrome}} --- hermanski-pudlak syndrome
{{MeshNumber|C18.452.648.066.102.600|Piebaldism}} --- piebaldism
{{MeshNumber|C18.452.648.066.187|Alkaptonuria}} --- alkaptonuria
{{MeshNumber|C18.452.648.066.210|Aminoaciduria,+Renal}} --- aminoaciduria, renal
{{MeshNumber|C18.452.648.066.210.250|Cystinuria}} --- cystinuria
{{MeshNumber|C18.452.648.066.210.490|Hartnup+Disease}} --- hartnup disease
{{MeshNumber|C18.452.648.066.275|Carbamoyl-Phosphate+Synthase+I+Deficiency+Disease}} --- carbamoyl-phosphate synthase i deficiency disease
{{MeshNumber|C18.452.648.066.340|Citrullinemia}} --- citrullinemia
{{MeshNumber|C18.452.648.066.470|Homocystinuria}} --- homocystinuria
{{MeshNumber|C18.452.648.066.475|Hyperargininemia}} --- hyperargininemia
{{MeshNumber|C18.452.648.066.477|Hyperglycinemia,+Nonketotic}} --- hyperglycinemia, nonketotic
{{MeshNumber|C18.452.648.066.480|Hyperhomocysteinemia}} --- hyperhomocysteinemia
{{MeshNumber|C18.452.648.066.544|Hyperlysinemias}} --- hyperlysinemias
{{MeshNumber|C18.452.648.066.608|Maple+Syrup+Urine+Disease}} --- maple syrup urine disease
{{MeshNumber|C18.452.648.066.620|Multiple+Carboxylase+Deficiency}} --- multiple carboxylase deficiency
{{MeshNumber|C18.452.648.066.620.100|Biotinidase+Deficiency}} --- biotinidase deficiency
{{MeshNumber|C18.452.648.066.620.380|Holocarboxylase+Synthetase+Deficiency}} --- holocarboxylase synthetase deficiency
{{MeshNumber|C18.452.648.066.729|Ornithine+Carbamoyltransferase+Deficiency+Disease}} --- ornithine carbamoyltransferase deficiency disease
{{MeshNumber|C18.452.648.066.766|Phenylketonurias}} --- phenylketonurias
{{MeshNumber|C18.452.648.066.766.500|Phenylketonuria,+Maternal}} --- phenylketonuria, maternal
{{MeshNumber|C18.452.648.066.880|Tyrosinemias}} --- tyrosinemias
{{MeshNumber|C18.452.648.088|Amino+Acid+Transport+Disorders,+Inborn}} --- amino acid transport disorders, inborn
{{MeshNumber|C18.452.648.088.400|Hartnup+Disease}} --- hartnup disease
{{MeshNumber|C18.452.648.088.600|Oculocerebrorenal+Syndrome}} --- oculocerebrorenal syndrome
{{MeshNumber|C18.452.648.100|Amyloidosis,+Familial}} --- amyloidosis, familial
{{MeshNumber|C18.452.648.100.050|Amyloid+Neuropathies,+Familial}} --- amyloid neuropathies, familial
{{MeshNumber|C18.452.648.100.160|Cerebral+Amyloid+Angiopathy,+Familial}} --- cerebral amyloid angiopathy, familial
{{MeshNumber|C18.452.648.151|Brain+Diseases,+Metabolic,+Inborn}} --- brain diseases, metabolic, inborn
{{MeshNumber|C18.452.648.151.050|Abetalipoproteinemia}} --- abetalipoproteinemia
{{MeshNumber|C18.452.648.151.162|Carbamoyl-Phosphate+Synthase+I+Deficiency+Disease}} --- carbamoyl-phosphate synthase i deficiency disease
{{MeshNumber|C18.452.648.151.168|Cerebral+Amyloid+Angiopathy,+Familial}} --- cerebral amyloid angiopathy, familial
{{MeshNumber|C18.452.648.151.175|Citrullinemia}} --- citrullinemia
{{MeshNumber|C18.452.648.151.300|Fucosidosis}} --- fucosidosis
{{MeshNumber|C18.452.648.151.320|Galactosemias}} --- galactosemias
{{MeshNumber|C18.452.648.151.330|Glycogen+Storage+Disease+Type+II}} --- glycogen storage disease type ii
{{MeshNumber|C18.452.648.151.355|Hartnup+Disease}} --- hartnup disease
{{MeshNumber|C18.452.648.151.360|Hepatolenticular+Degeneration}} --- hepatolenticular degeneration
{{MeshNumber|C18.452.648.151.365|Homocystinuria}} --- homocystinuria
{{MeshNumber|C18.452.648.151.370|Hyperargininemia}} --- hyperargininemia
{{MeshNumber|C18.452.648.151.375|Hyperglycinemia,+Nonketotic}} --- hyperglycinemia, nonketotic
{{MeshNumber|C18.452.648.151.380|Hyperlysinemias}} --- hyperlysinemias
{{MeshNumber|C18.452.648.151.412|Leigh+Disease}} --- leigh disease
{{MeshNumber|C18.452.648.151.425|Lesch-Nyhan+Syndrome}} --- lesch-nyhan syndrome
{{MeshNumber|C18.452.648.151.435|Lysosomal+Storage+Diseases,+Nervous+System}} --- lysosomal storage diseases, nervous system
{{MeshNumber|C18.452.648.151.435.295|Fucosidosis}} --- fucosidosis
{{MeshNumber|C18.452.648.151.435.340|Glycogen+Storage+Disease+Type+II}} --- glycogen storage disease type ii
{{MeshNumber|C18.452.648.151.435.590|Mucolipidoses}} --- mucolipidoses
{{MeshNumber|C18.452.648.151.435.810|Sialic+Acid+Storage+Disease}} --- sialic acid storage disease
{{MeshNumber|C18.452.648.151.435.825|Sphingolipidoses}} --- sphingolipidoses
{{MeshNumber|C18.452.648.151.435.825.200|Fabry+Disease}} --- fabry disease
{{MeshNumber|C18.452.648.151.435.825.300|Gangliosidoses}} --- gangliosidoses
{{MeshNumber|C18.452.648.151.435.825.300.300|Gangliosidoses+GM2}} --- gangliosidoses gm2
{{MeshNumber|C18.452.648.151.435.825.300.300.800|Sandhoff+Disease}} --- sandhoff disease
{{MeshNumber|C18.452.648.151.435.825.300.300.840|Tay-Sachs+Disease}} --- tay-sachs disease
{{MeshNumber|C18.452.648.151.435.825.300.300.920|Tay-Sachs+Disease,+AB+Variant}} --- tay-sachs disease, ab variant
{{MeshNumber|C18.452.648.151.435.825.300.400|Gangliosidosis+GM1}} --- gangliosidosis gm1
{{MeshNumber|C18.452.648.151.435.825.400|Gaucher+Disease}} --- gaucher disease
{{MeshNumber|C18.452.648.151.435.825.590|Leukodystrophy,+Globoid+Cell}} --- leukodystrophy, globoid cell
{{MeshNumber|C18.452.648.151.435.825.594|Leukodystrophy,+Metachromatic}} --- leukodystrophy, metachromatic
{{MeshNumber|C18.452.648.151.435.825.700|Niemann-Pick+Diseases}} --- niemann-pick diseases
{{MeshNumber|C18.452.648.151.445|Maple+Syrup+Urine+Disease}} --- maple syrup urine disease
{{MeshNumber|C18.452.648.151.447|MELAS+Syndrome}} --- melas syndrome
{{MeshNumber|C18.452.648.151.450|Menkes+Kinky+Hair+Syndrome}} --- menkes kinky hair syndrome
{{MeshNumber|C18.452.648.151.505|MERRF+Syndrome}} --- merrf syndrome
{{MeshNumber|C18.452.648.151.580|Mucolipidoses}} --- mucolipidoses
{{MeshNumber|C18.452.648.151.640|Oculocerebrorenal+Syndrome}} --- oculocerebrorenal syndrome
{{MeshNumber|C18.452.648.151.650|Ornithine+Carbamoyltransferase+Deficiency+Disease}} --- ornithine carbamoyltransferase deficiency disease
{{MeshNumber|C18.452.648.151.680|Peroxisomal+Disorders}} --- peroxisomal disorders
{{MeshNumber|C18.452.648.151.680.100|Adrenoleukodystrophy}} --- adrenoleukodystrophy
{{MeshNumber|C18.452.648.151.680.760|Refsum+Disease}} --- refsum disease
{{MeshNumber|C18.452.648.151.680.970|Zellweger+Syndrome}} --- zellweger syndrome
{{MeshNumber|C18.452.648.151.687|Phenylketonurias}} --- phenylketonurias
{{MeshNumber|C18.452.648.151.687.500|Phenylketonuria,+Maternal}} --- phenylketonuria, maternal
{{MeshNumber|C18.452.648.151.725|Pyruvate+Carboxylase+Deficiency+Disease}} --- pyruvate carboxylase deficiency disease
{{MeshNumber|C18.452.648.151.750|Pyruvate+Dehydrogenase+Complex+Deficiency+Disease}} --- pyruvate dehydrogenase complex deficiency disease
{{MeshNumber|C18.452.648.151.825|Sphingolipidoses}} --- sphingolipidoses
{{MeshNumber|C18.452.648.151.825.200|Fabry+Disease}} --- fabry disease
{{MeshNumber|C18.452.648.151.825.300|Gangliosidoses}} --- gangliosidoses
{{MeshNumber|C18.452.648.151.825.300.300|Gangliosidoses+GM2}} --- gangliosidoses gm2
{{MeshNumber|C18.452.648.151.825.300.300.700|Sandhoff+Disease}} --- sandhoff disease
{{MeshNumber|C18.452.648.151.825.300.300.850|Tay-Sachs+Disease}} --- tay-sachs disease
{{MeshNumber|C18.452.648.151.825.300.300.925|Tay-Sachs+Disease,+AB+Variant}} --- tay-sachs disease, ab variant
{{MeshNumber|C18.452.648.151.825.300.400|Gangliosidosis+GM1}} --- gangliosidosis gm1
{{MeshNumber|C18.452.648.151.825.400|Gaucher+Disease}} --- gaucher disease
{{MeshNumber|C18.452.648.151.825.590|Leukodystrophy,+Globoid+Cell}} --- leukodystrophy, globoid cell
{{MeshNumber|C18.452.648.151.825.594|Leukodystrophy,+Metachromatic}} --- leukodystrophy, metachromatic
{{MeshNumber|C18.452.648.151.825.700|Niemann-Pick+Diseases}} --- niemann-pick diseases
{{MeshNumber|C18.452.648.151.875|Tyrosinemias}} --- tyrosinemias
{{MeshNumber|C18.452.648.202|Carbohydrate+Metabolism,+Inborn+Errors}} --- carbohydrate metabolism, inborn errors
{{MeshNumber|C18.452.648.202.125|Carbohydrate-Deficient+Glycoprotein+Syndrome}} --- carbohydrate-deficient glycoprotein syndrome
{{MeshNumber|C18.452.648.202.251|Fructose+Metabolism,+Inborn+Errors}} --- fructose metabolism, inborn errors
{{MeshNumber|C18.452.648.202.251.221|Fructose-1,6-Diphosphatase+Deficiency}} --- fructose-1,6-diphosphatase deficiency
{{MeshNumber|C18.452.648.202.251.271|Fructose+Intolerance}} --- Hereditary fructose intolerance
{{MeshNumber|C18.452.648.202.303|Fucosidosis}} --- fucosidosis
{{MeshNumber|C18.452.648.202.355|Galactosemias}} --- galactosemias
{{MeshNumber|C18.452.648.202.449|Glycogen+Storage+Disease}} --- glycogen storage disease
{{MeshNumber|C18.452.648.202.449.448|Glycogen+Storage+Disease+Type+I}} --- glycogen storage disease type i
{{MeshNumber|C18.452.648.202.449.500|Glycogen+Storage+Disease+Type+II}} --- glycogen storage disease type ii
{{MeshNumber|C18.452.648.202.449.510|Glycogen+Storage+Disease+Type+IIb}} --- glycogen storage disease type iib
{{MeshNumber|C18.452.648.202.449.520|Glycogen+Storage+Disease+Type+III}} --- glycogen storage disease type iii
{{MeshNumber|C18.452.648.202.449.540|Glycogen+Storage+Disease+Type+IV}} --- glycogen storage disease type iv
{{MeshNumber|C18.452.648.202.449.560|Glycogen+Storage+Disease+Type+V}} --- glycogen storage disease type v
{{MeshNumber|C18.452.648.202.449.580|Glycogen+Storage+Disease+Type+VI}} --- glycogen storage disease type vi
{{MeshNumber|C18.452.648.202.449.600|Glycogen+Storage+Disease+Type+VII}} --- glycogen storage disease type vii
{{MeshNumber|C18.452.648.202.449.620|Glycogen+Storage+Disease+Type+VIII}} --- glycogen storage disease type viii
{{MeshNumber|C18.452.648.202.460|Hyperoxaluria,+Primary}} --- hyperoxaluria, primary
{{MeshNumber|C18.452.648.202.589|Lactose+Intolerance}} --- lactose intolerance
{{MeshNumber|C18.452.648.202.607|Mannosidase+Deficiency+Diseases}} --- mannosidase deficiency diseases
{{MeshNumber|C18.452.648.202.607.500|alpha-Mannosidosis}} --- alpha-mannosidosis
{{MeshNumber|C18.452.648.202.607.750|beta-Mannosidosis}} --- beta-mannosidosis
{{MeshNumber|C18.452.648.202.670|Mucolipidoses}} --- mucolipidoses
{{MeshNumber|C18.452.648.202.715|Mucopolysaccharidoses}} --- mucopolysaccharidoses
{{MeshNumber|C18.452.648.202.715.640|Mucopolysaccharidosis+I}} --- mucopolysaccharidosis i
{{MeshNumber|C18.452.648.202.715.645|Mucopolysaccharidosis+II}} --- mucopolysaccharidosis ii
{{MeshNumber|C18.452.648.202.715.650|Mucopolysaccharidosis+III}} --- mucopolysaccharidosis iii
{{MeshNumber|C18.452.648.202.715.655|Mucopolysaccharidosis+IV}} --- mucopolysaccharidosis iv
{{MeshNumber|C18.452.648.202.715.670|Mucopolysaccharidosis+VI}} --- mucopolysaccharidosis vi
{{MeshNumber|C18.452.648.202.715.675|Mucopolysaccharidosis+VII}} --- mucopolysaccharidosis vii
{{MeshNumber|C18.452.648.202.720|Multiple+Carboxylase+Deficiency}} --- multiple carboxylase deficiency
{{MeshNumber|C18.452.648.202.720.100|Biotinidase+Deficiency}} --- biotinidase deficiency
{{MeshNumber|C18.452.648.202.720.380|Holocarboxylase+Synthetase+Deficiency}} --- holocarboxylase synthetase deficiency
{{MeshNumber|C18.452.648.202.810|Pyruvate+Metabolism,+Inborn+Errors}} --- pyruvate metabolism, inborn errors
{{MeshNumber|C18.452.648.202.810.444|Leigh+Disease}} --- leigh disease
{{MeshNumber|C18.452.648.202.810.666|Pyruvate+Carboxylase+Deficiency+Disease}} --- pyruvate carboxylase deficiency disease
{{MeshNumber|C18.452.648.202.810.766|Pyruvate+Dehydrogenase+Complex+Deficiency+Disease}} --- pyruvate dehydrogenase complex deficiency disease
{{MeshNumber|C18.452.648.240|Cytochrome-c+Oxidase+Deficiency}} --- cytochrome-c oxidase deficiency
{{MeshNumber|C18.452.648.390|Glucosephosphate+Dehydrogenase+Deficiency}} --- glucosephosphate dehydrogenase deficiency
{{MeshNumber|C18.452.648.437|Hyperbilirubinemia,+Hereditary}} --- hyperbilirubinemia, hereditary
{{MeshNumber|C18.452.648.437.281|Crigler-Najjar+Syndrome}} --- crigler-najjar syndrome
{{MeshNumber|C18.452.648.437.528|Gilbert+Disease}} --- gilbert disease
{{MeshNumber|C18.452.648.499|Jaundice,+Chronic+Idiopathic}} --- jaundice, chronic idiopathic
{{MeshNumber|C18.452.648.556|Lipid+Metabolism,+Inborn+Errors}} --- lipid metabolism, inborn errors
{{MeshNumber|C18.452.648.556.475|Hypercholesterolemia,+Familial}} --- hypercholesterolemia, familial
{{MeshNumber|C18.452.648.556.480|Hyperlipidemia,+Familial+Combined}} --- hyperlipidemia, familial combined
{{MeshNumber|C18.452.648.556.480.390|Hypercholesterolemia,+Familial}} --- hypercholesterolemia, familial
{{MeshNumber|C18.452.648.556.480.395|Hyperlipoproteinemia+Type+IV}} --- hyperlipoproteinemia type iv
{{MeshNumber|C18.452.648.556.484|Hyperlipoproteinemia+Type+III}} --- hyperlipoproteinemia type iii
{{MeshNumber|C18.452.648.556.490|Hyperlipoproteinemia+Type+IV}} --- hyperlipoproteinemia type iv
{{MeshNumber|C18.452.648.556.495|Hyperlipoproteinemia+Type+V}} --- hyperlipoproteinemia type v
{{MeshNumber|C18.452.648.556.500|Hypolipoproteinemia}} --- hypolipoproteinemia
{{MeshNumber|C18.452.648.556.500.220|Abetalipoproteinemia}} --- abetalipoproteinemia
{{MeshNumber|C18.452.648.556.500.440|Hypobetalipoproteinemia}} --- hypobetalipoproteinemia
{{MeshNumber|C18.452.648.556.500.448|Lecithin+Acyltransferase+Deficiency}} --- lecithin acyltransferase deficiency
{{MeshNumber|C18.452.648.556.500.724|Tangier+Disease}} --- tangier disease
{{MeshNumber|C18.452.648.556.641|Lipoidosis}} --- lipoidosis
{{MeshNumber|C18.452.648.556.641.201|Cholesterol+Ester+Storage+Disease}} --- cholesterol ester storage disease
{{MeshNumber|C18.452.648.556.641.391|Lipoidproteinosis}} --- lipoidproteinosis
{{MeshNumber|C18.452.648.556.641.509|Neuronal+Ceroid-Lipofuscinosis}} --- neuronal ceroid-lipofuscinosis
{{MeshNumber|C18.452.648.556.641.643|Refsum+Disease}} --- refsum disease
{{MeshNumber|C18.452.648.556.641.723|Sjogren-Larsson+Syndrome}} --- sjogren-larsson syndrome
{{MeshNumber|C18.452.648.556.641.803|Sphingolipidoses}} --- sphingolipidoses
{{MeshNumber|C18.452.648.556.641.803.300|Fabry+Disease}} --- fabry disease
{{MeshNumber|C18.452.648.556.641.803.350|Gangliosidoses}} --- gangliosidoses
{{MeshNumber|C18.452.648.556.641.803.350.300|Gangliosidoses+GM2}} --- gangliosidoses gm2
{{MeshNumber|C18.452.648.556.641.803.350.300.700|Sandhoff+Disease}} --- sandhoff disease
{{MeshNumber|C18.452.648.556.641.803.350.300.850|Tay-Sachs+Disease}} --- tay-sachs disease
{{MeshNumber|C18.452.648.556.641.803.350.300.925|Tay-Sachs+Disease,+AB+Variant}} --- tay-sachs disease, ab variant
{{MeshNumber|C18.452.648.556.641.803.350.360|Gangliosidosis+GM1}} --- gangliosidosis gm1
{{MeshNumber|C18.452.648.556.641.803.441|Gaucher+Disease}} --- gaucher disease
{{MeshNumber|C18.452.648.556.641.803.585|Leukodystrophy,+Globoid+Cell}} --- leukodystrophy, globoid cell
{{MeshNumber|C18.452.648.556.641.803.594|Leukodystrophy,+Metachromatic}} --- leukodystrophy, metachromatic
{{MeshNumber|C18.452.648.556.641.803.730|Niemann-Pick+Diseases}} --- niemann-pick diseases
{{MeshNumber|C18.452.648.556.641.803.850|Sea-Blue+Histiocyte+Syndrome}} --- sea-blue histiocyte syndrome
{{MeshNumber|C18.452.648.556.641.923|Wolman+Disease}} --- wolman disease
{{MeshNumber|C18.452.648.556.645|Lipoprotein+Lipase+Deficiency,+Familial}} --- lipoprotein lipase deficiency, familial
{{MeshNumber|C18.452.648.556.750|Peroxisomal+Disorders}} --- peroxisomal disorders
{{MeshNumber|C18.452.648.556.750.025|Acatalasia}} --- acatalasia
{{MeshNumber|C18.452.648.556.750.112|Adrenoleukodystrophy}} --- adrenoleukodystrophy
{{MeshNumber|C18.452.648.556.750.200|Chondrodysplasia+Punctata,+Rhizomelic}} --- chondrodysplasia punctata, rhizomelic
{{MeshNumber|C18.452.648.556.750.760|Refsum+Disease}} --- refsum disease
{{MeshNumber|C18.452.648.556.750.970|Zellweger+Syndrome}} --- zellweger syndrome
{{MeshNumber|C18.452.648.556.850|Smith-Lemli-Opitz+Syndrome}} --- smith-lemli-opitz syndrome
{{MeshNumber|C18.452.648.556.925|Xanthomatosis,+Cerebrotendinous}} --- xanthomatosis, cerebrotendinous
{{MeshNumber|C18.452.648.595|Lysosomal+Storage+Diseases}} --- lysosomal storage diseases
{{MeshNumber|C18.452.648.595.201|Cholesterol+Ester+Storage+Disease}} --- cholesterol ester storage disease
{{MeshNumber|C18.452.648.595.554|Lysosomal+Storage+Diseases,+Nervous+System}} --- lysosomal storage diseases, nervous system
{{MeshNumber|C18.452.648.595.554.295|Fucosidosis}} --- fucosidosis
{{MeshNumber|C18.452.648.595.554.340|Glycogen+Storage+Disease+Type+II}} --- glycogen storage disease type ii
{{MeshNumber|C18.452.648.595.554.590|Mucolipidoses}} --- mucolipidoses
{{MeshNumber|C18.452.648.595.554.810|Sialic+Acid+Storage+Disease}} --- sialic acid storage disease
{{MeshNumber|C18.452.648.595.554.825|Sphingolipidoses}} --- sphingolipidoses
{{MeshNumber|C18.452.648.595.554.825.200|Fabry+Disease}} --- fabry disease
{{MeshNumber|C18.452.648.595.554.825.300|Gangliosidoses}} --- gangliosidoses
{{MeshNumber|C18.452.648.595.554.825.300.300|Gangliosidoses+GM2}} --- gangliosidoses gm2
{{MeshNumber|C18.452.648.595.554.825.300.300.800|Sandhoff+Disease}} --- sandhoff disease
{{MeshNumber|C18.452.648.595.554.825.300.300.840|Tay-Sachs+Disease}} --- tay-sachs disease
{{MeshNumber|C18.452.648.595.554.825.300.300.920|Tay-Sachs+Disease,+AB+Variant}} --- tay-sachs disease, ab variant
{{MeshNumber|C18.452.648.595.554.825.300.400|Gangliosidosis+GM1}} --- gangliosidosis gm1
{{MeshNumber|C18.452.648.595.554.825.400|Gaucher+Disease}} --- gaucher disease
{{MeshNumber|C18.452.648.595.554.825.590|Leukodystrophy,+Globoid+Cell}} --- leukodystrophy, globoid cell
{{MeshNumber|C18.452.648.595.554.825.594|Leukodystrophy,+Metachromatic}} --- leukodystrophy, metachromatic
{{MeshNumber|C18.452.648.595.554.825.700|Niemann-Pick+Diseases}} --- niemann-pick diseases
{{MeshNumber|C18.452.648.595.577|Mannosidase+Deficiency+Diseases}} --- mannosidase deficiency diseases
{{MeshNumber|C18.452.648.595.577.500|alpha-Mannosidosis}} --- alpha-mannosidosis
{{MeshNumber|C18.452.648.595.577.750|beta-Mannosidosis}} --- beta-mannosidosis
{{MeshNumber|C18.452.648.595.600|Mucopolysaccharidoses}} --- mucopolysaccharidoses
{{MeshNumber|C18.452.648.595.600.640|Mucopolysaccharidosis+I}} --- mucopolysaccharidosis i
{{MeshNumber|C18.452.648.595.600.645|Mucopolysaccharidosis+II}} --- mucopolysaccharidosis ii
{{MeshNumber|C18.452.648.595.600.650|Mucopolysaccharidosis+III}} --- mucopolysaccharidosis iii
{{MeshNumber|C18.452.648.595.600.655|Mucopolysaccharidosis+IV}} --- mucopolysaccharidosis iv
{{MeshNumber|C18.452.648.595.600.670|Mucopolysaccharidosis+VI}} --- mucopolysaccharidosis vi
{{MeshNumber|C18.452.648.595.600.675|Mucopolysaccharidosis+VII}} --- mucopolysaccharidosis vii
{{MeshNumber|C18.452.648.595.803|Sphingolipidoses}} --- sphingolipidoses
{{MeshNumber|C18.452.648.595.803.300|Fabry+Disease}} --- fabry disease
{{MeshNumber|C18.452.648.595.803.350|Gangliosidoses}} --- gangliosidoses
{{MeshNumber|C18.452.648.595.803.350.300|Gangliosidoses+GM2}} --- gangliosidoses gm2
{{MeshNumber|C18.452.648.595.803.350.300.700|Sandhoff+Disease}} --- sandhoff disease
{{MeshNumber|C18.452.648.595.803.350.300.850|Tay-Sachs+Disease}} --- tay-sachs disease
{{MeshNumber|C18.452.648.595.803.350.300.925|Tay-Sachs+Disease,+AB+Variant}} --- tay-sachs disease, ab variant
{{MeshNumber|C18.452.648.595.803.441|Gaucher+Disease}} --- gaucher disease
{{MeshNumber|C18.452.648.595.803.585|Leukodystrophy,+Globoid+Cell}} --- leukodystrophy, globoid cell
{{MeshNumber|C18.452.648.595.803.594|Leukodystrophy,+Metachromatic}} --- leukodystrophy, metachromatic
{{MeshNumber|C18.452.648.595.803.730|Niemann-Pick+Diseases}} --- niemann-pick diseases
{{MeshNumber|C18.452.648.595.803.850|Sea-Blue+Histiocyte+Syndrome}} --- sea-blue histiocyte syndrome
{{MeshNumber|C18.452.648.595.923|Wolman+Disease}} --- wolman disease
{{MeshNumber|C18.452.648.618|Metal+Metabolism,+Inborn+Errors}} --- metal metabolism, inborn errors
{{MeshNumber|C18.452.648.618.337|Hemochromatosis}} --- hemochromatosis
{{MeshNumber|C18.452.648.618.403|Hepatolenticular+Degeneration}} --- hepatolenticular degeneration
{{MeshNumber|C18.452.648.618.482|Hypophosphatasia}} --- hypophosphatasia
{{MeshNumber|C18.452.648.618.544|Hypophosphatemia,+Familial}} --- hypophosphatemia, familial
{{MeshNumber|C18.452.648.618.590|Menkes+Kinky+Hair+Syndrome}} --- menkes kinky hair syndrome
{{MeshNumber|C18.452.648.618.711|Paralyses,+Familial+Periodic}} --- paralyses, familial periodic
{{MeshNumber|C18.452.648.618.711.550|Hypokalemic+Periodic+Paralysis}} --- hypokalemic periodic paralysis
{{MeshNumber|C18.452.648.618.711.600|Paralysis,+Hyperkalemic+Periodic}} --- paralysis, hyperkalemic periodic
{{MeshNumber|C18.452.648.618.815|Pseudohypoparathyroidism}} --- pseudohypoparathyroidism
{{MeshNumber|C18.452.648.618.815.815|Pseudopseudohypoparathyroidism}} --- pseudopseudohypoparathyroidism
{{MeshNumber|C18.452.648.730|Porphyria,+Erythropoietic}} --- porphyria, erythropoietic
{{MeshNumber|C18.452.648.735|Porphyrias,+Hepatic}} --- porphyrias, hepatic
{{MeshNumber|C18.452.648.735.074|Coproporphyria,+Hereditary}} --- coproporphyria, hereditary
{{MeshNumber|C18.452.648.735.150|Porphyria,+Acute+Intermittent}} --- porphyria, acute intermittent
{{MeshNumber|C18.452.648.735.250|Porphyria+Cutanea+Tarda}} --- porphyria cutanea tarda
{{MeshNumber|C18.452.648.735.437|Porphyria,+Hepatoerythropoietic}} --- porphyria, hepatoerythropoietic
{{MeshNumber|C18.452.648.735.625|Porphyria,+Variegate}} --- porphyria, variegate
{{MeshNumber|C18.452.648.735.812|Protoporphyria,+Erythropoietic}} --- protoporphyria, erythropoietic
{{MeshNumber|C18.452.648.769|Progeria}} --- progeria
{{MeshNumber|C18.452.648.798|Purine-Pyrimidine+Metabolism,+Inborn+Errors}} --- purine-pyrimidine metabolism, inborn errors
{{MeshNumber|C18.452.648.798.368|Gout}} --- gout
{{MeshNumber|C18.452.648.798.368.410|Arthritis,+Gouty}} --- arthritis, gouty
{{MeshNumber|C18.452.648.798.594|Lesch-Nyhan+Syndrome}} --- lesch-nyhan syndrome
{{MeshNumber|C18.452.648.851|Renal+Tubular+Transport,+Inborn+Errors}} --- renal tubular transport, inborn errors
{{MeshNumber|C18.452.648.851.093|Acidosis,+Renal+Tubular}} --- acidosis, renal tubular
{{MeshNumber|C18.452.648.851.191|Aminoaciduria,+Renal}} --- aminoaciduria, renal
{{MeshNumber|C18.452.648.851.191.250|Cystinuria}} --- cystinuria
{{MeshNumber|C18.452.648.851.191.457|Hartnup+Disease}} --- hartnup disease
{{MeshNumber|C18.452.648.851.368|Cystinosis}} --- cystinosis
{{MeshNumber|C18.452.648.851.368.210|Fanconi+Syndrome}} --- fanconi syndrome
{{MeshNumber|C18.452.648.851.532|Glycosuria,+Renal}} --- glycosuria, renal
{{MeshNumber|C18.452.648.851.647|Hypophosphatemia,+Familial}} --- hypophosphatemia, familial
{{MeshNumber|C18.452.648.851.750|Oculocerebrorenal+Syndrome}} --- oculocerebrorenal syndrome
{{MeshNumber|C18.452.648.851.770|Pseudohypoaldosteronism}} --- pseudohypoaldosteronism
{{MeshNumber|C18.452.648.925|Steroid+Metabolism,+Inborn+Errors}} --- steroid metabolism, inborn errors
{{MeshNumber|C18.452.648.925.249|Adrenal+Hyperplasia,+Congenital}} --- adrenal hyperplasia, congenital
{{MeshNumber|C18.452.648.925.500|Mineralocorticoid+Excess+Syndrome,+Apparent}} --- mineralocorticoid excess syndrome, apparent
{{MeshNumber|C18.452.648.925.750|Ichthyosis,+X-Linked}} --- ichthyosis, x-linked
{{MeshNumber|C18.452.648.925.875|Smith-Lemli-Opitz+Syndrome}} --- smith-lemli-opitz syndrome

{{MeshNumber|C18.452.660|Mitochondrial+Diseases}} --- mitochondrial diseases

{{MeshNumber|C18.452.660.195|Cytochrome-c+Oxidase+Deficiency}} --- cytochrome-c oxidase deficiency
{{MeshNumber|C18.452.660.300|Friedreich+Ataxia}} --- friedreich ataxia
{{MeshNumber|C18.452.660.515|Optic+Atrophy,+Hereditary,+Leber}} --- optic atrophy, hereditary, leber
{{MeshNumber|C18.452.660.520|Leigh+Disease}} --- leigh disease
{{MeshNumber|C18.452.660.560|Mitochondrial+Myopathies}} --- mitochondrial myopathies
{{MeshNumber|C18.452.660.560.620|Mitochondrial+Encephalomyopathies}} --- mitochondrial encephalomyopathies
{{MeshNumber|C18.452.660.560.620.520|MELAS+Syndrome}} --- melas syndrome
{{MeshNumber|C18.452.660.560.620.530|MERRF+Syndrome}} --- merrf syndrome
{{MeshNumber|C18.452.660.560.700|Ophthalmoplegia,+Chronic+Progressive+External}} --- ophthalmoplegia, chronic progressive external
{{MeshNumber|C18.452.660.560.700.500|Kearns-Sayer+Syndrome}} --- kearns-sayer syndrome
{{MeshNumber|C18.452.660.665|Optic+Atrophy,+Autosomal+Dominant}} --- optic atrophy, autosomal dominant
{{MeshNumber|C18.452.660.705|Pyruvate+Carboxylase+Deficiency+Disease}} --- pyruvate carboxylase deficiency disease
{{MeshNumber|C18.452.660.710|Pyruvate+Dehydrogenase+Complex+Deficiency+Disease}} --- pyruvate dehydrogenase complex deficiency disease

{{MeshNumber|C18.452.730|Ochronosis}} --- ochronosis

{{MeshNumber|C18.452.750|Phosphorus+Metabolism+Disorders}} --- phosphorus metabolism disorders

{{MeshNumber|C18.452.750.400|Hypophosphatemia}} --- hypophosphatemia

{{MeshNumber|C18.452.872|Skin+Diseases,+Metabolic}} --- skin diseases, metabolic

{{MeshNumber|C18.452.872.077|Adiposis+Dolorosa}} --- adiposis dolorosa
{{MeshNumber|C18.452.872.617|Porphyrias}} --- porphyrias
{{MeshNumber|C18.452.872.617.250|Porphyria,+Erythropoietic}} --- porphyria, erythropoietic
{{MeshNumber|C18.452.872.617.400|Porphyrias,+Hepatic}} --- porphyrias, hepatic
{{MeshNumber|C18.452.872.617.400.074|Coproporphyria,+Hereditary}} --- coproporphyria, hereditary
{{MeshNumber|C18.452.872.617.400.150|Porphyria,+Acute+Intermittent}} --- porphyria, acute intermittent
{{MeshNumber|C18.452.872.617.400.250|Porphyria+Cutanea+Tarda}} --- porphyria cutanea tarda
{{MeshNumber|C18.452.872.617.400.437|Porphyria,+Hepatoerythropoietic}} --- porphyria, hepatoerythropoietic
{{MeshNumber|C18.452.872.617.400.625|Porphyria,+Variegate}} --- porphyria, variegate
{{MeshNumber|C18.452.872.617.400.812|Protoporphyria,+Erythropoietic}} --- protoporphyria, erythropoietic
{{MeshNumber|C18.452.872.866|Xanthogranuloma,+Juvenile}} --- xanthogranuloma, juvenile
{{MeshNumber|C18.452.872.929|Xanthomatosis}} --- xanthomatosis
{{MeshNumber|C18.452.872.929.950|Wolman+Disease}} --- wolman disease
{{MeshNumber|C18.452.872.929.975|Xanthomatosis,+Cerebrotendinous}} --- xanthomatosis, cerebrotendinous

{{MeshNumber|C18.452.940|Wasting+Syndrome}} --- wasting syndrome

{{MeshNumber|C18.452.940.520|HIV+Wasting+Syndrome}} --- hiv wasting syndrome

{{MeshNumber|C18.452.950|Water-Electrolyte+Imbalance}} --- water-electrolyte imbalance

{{MeshNumber|C18.452.950.179|Dehydration}} --- dehydration
{{MeshNumber|C18.452.950.340|Hypercalcemia}} --- hypercalcemia
{{MeshNumber|C18.452.950.396|Hyperkalemia}} --- hyperkalemia
{{MeshNumber|C18.452.950.452|Hypernatremia}} --- hypernatremia
{{MeshNumber|C18.452.950.509|Hypocalcemia}} --- hypocalcemia
{{MeshNumber|C18.452.950.565|Hypokalemia}} --- hypokalemia
{{MeshNumber|C18.452.950.620|Hyponatremia}} --- hyponatremia
{{MeshNumber|C18.452.950.626|Inappropriate+ADH+Syndrome}} --- inappropriate adh syndrome
{{MeshNumber|C18.452.950.932|Water+Intoxication}} --- water intoxication

{{MeshNumber|C18.654|Nutrition+Disorders}} --- nutrition disorders

{{MeshNumber|C18.654.180|Child+Nutrition+Disorders}} --- child nutrition disorders

{{MeshNumber|C18.654.422|Infant+Nutrition+Disorders}} --- infant nutrition disorders

{{MeshNumber|C18.654.422.360|Hemorrhagic+Disease+of+Newborn}} --- hemorrhagic disease of newborn

{{MeshNumber|C18.654.521|Malnutrition}} --- malnutrition

{{MeshNumber|C18.654.521.500|Deficiency+Diseases}} --- deficiency diseases
{{MeshNumber|C18.654.521.500.133|Avitaminosis}} --- avitaminosis
{{MeshNumber|C18.654.521.500.133.115|Ascorbic+Acid+Deficiency}} --- ascorbic acid deficiency
{{MeshNumber|C18.654.521.500.133.115.661|Scurvy}} --- scurvy
{{MeshNumber|C18.654.521.500.133.628|Vitamin+A+Deficiency}} --- vitamin A deficiency
{{MeshNumber|C18.654.521.500.133.699|Vitamin+B+Deficiency}} --- vitamin B deficiency
{{MeshNumber|C18.654.521.500.133.699.160|Choline+Deficiency}} --- choline deficiency
{{MeshNumber|C18.654.521.500.133.699.308|Folic+Acid+Deficiency}} --- folic acid deficiency
{{MeshNumber|C18.654.521.500.133.699.529|Pellagra}} --- pellagra
{{MeshNumber|C18.654.521.500.133.699.713|Riboflavin+Deficiency}} --- riboflavin deficiency
{{MeshNumber|C18.654.521.500.133.699.827|Thiamine+Deficiency}} --- thiamine deficiency
{{MeshNumber|C18.654.521.500.133.699.827.223|Beriberi}} --- beriberi
{{MeshNumber|C18.654.521.500.133.699.827.822|Wernicke+Encephalopathy}} --- wernicke encephalopathy
{{MeshNumber|C18.654.521.500.133.699.901|Vitamin+B+6+Deficiency}} --- vitamin B6 deficiency
{{MeshNumber|C18.654.521.500.133.699.923|Vitamin+B+12+Deficiency}} --- vitamin B12 deficiency
{{MeshNumber|C18.654.521.500.133.699.923.280|Anemia,+Pernicious}} --- anemia, pernicious
{{MeshNumber|C18.654.521.500.133.770|Vitamin+D+Deficiency}} --- vitamin D deficiency
{{MeshNumber|C18.654.521.500.133.770.496|Osteomalacia}} --- osteomalacia
{{MeshNumber|C18.654.521.500.133.770.734|Rickets}} --- rickets
{{MeshNumber|C18.654.521.500.133.841|Vitamin+E+Deficiency}} --- vitamin E deficiency
{{MeshNumber|C18.654.521.500.133.841.682|Steatitis}} --- steatitis
{{MeshNumber|C18.654.521.500.133.912|Vitamin+K+Deficiency}} --- vitamin K deficiency
{{MeshNumber|C18.654.521.500.133.912.360|Hemorrhagic+Disease+of+Newborn}} --- hemorrhagic disease of newborn
{{MeshNumber|C18.654.521.500.439|Magnesium+Deficiency}} --- magnesium deficiency
{{MeshNumber|C18.654.521.500.617|Potassium+Deficiency}} --- potassium deficiency
{{MeshNumber|C18.654.521.500.708|Protein+Deficiency}} --- protein deficiency
{{MeshNumber|C18.654.521.500.708.626|Protein-Energy+Malnutrition}} --- protein-energy malnutrition
{{MeshNumber|C18.654.521.500.708.626.505|Kwashiorkor}} --- kwashiorkor
{{MeshNumber|C18.654.521.500.857|Swayback}} --- swayback
{{MeshNumber|C18.654.521.625|Fetal+Nutrition+Disorders}} --- fetal nutrition disorders
{{MeshNumber|C18.654.521.750|Starvation}} --- starvation

{{MeshNumber|C18.654.726|Overnutrition}} --- overnutrition

{{MeshNumber|C18.654.726.500|Obesity}} --- obesity
{{MeshNumber|C18.654.726.500.695|Obesity+Hypoventilation+Syndrome}} --- obesity hypoventilation syndrome
{{MeshNumber|C18.654.726.500.700|Obesity,+Morbid}} --- obesity, morbid
{{MeshNumber|C18.654.726.500.740|Prader-Willi+Syndrome}} --- prader-willi syndrome

{{MeshNumber|C18.654.940|Wasting+Syndrome}} --- wasting syndrome

{{MeshNumber|C18.654.940.520|HIV+Wasting+Syndrome}} --- hiv wasting syndrome

1 : Medical Subject Headings

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