List of MeSH codes (C18)

– [nutritional and metabolic diseases]

– [metabolic diseases]

– [acid-base imbalance]

• – achlorhydria
• – acidosis
• – acidosis, lactic
• – acidosis, renal tubular
• – acidosis, respiratory
• – diabetic ketoacidosis
• – ketosis
• – alkalosis
• – alkalosis, respiratory

  – [amyloidosis]

• – amyloid neuropathies
• – amyloid neuropathies, familial
• – amyloidosis, familial
• – amyloid neuropathies, familial
• – cerebral amyloid angiopathy, familial
• – cerebral amyloid angiopathy
• – cerebral amyloid angiopathy, familial

  – [brain diseases, metabolic]

• – brain diseases, metabolic, inborn
• – abetalipoproteinemia
• – carbamoyl-phosphate synthase I deficiency disease
• – citrullinemia
• – galactosemias
• – Hartnup disease
• – hepatolenticular degeneration
• – homocystinuria
• – hyperargininemia
• – hyperglycinemia, nonketotic
• – hyperlysinemias
• – Leigh disease
• – Lesch–Nyhan syndrome
• – lysosomal storage diseases, nervous system
• – fucosidosis
• – glycogen storage disease type II
• – mucolipidoses
• – sialic acid storage disease
• – sphingolipidoses
• – fabry disease
• – gangliosidoses
• – gangliosidoses GM2
• – Sandhoff disease
• – Tay–Sachs disease
• – Tay–Sachs disease, AB variant
• – gangliosidosis gm1
• – Gaucher disease
• – leukodystrophy, globoid cell
• – leukodystrophy, metachromatic
• – Niemann–Pick diseases
• – maple syrup urine disease
• – MELAS syndrome
• – Menkes kinky hair syndrome
• – MERRF syndrome
• – oculocerebrorenal syndrome
• – ornithine carbamoyltransferase deficiency disease
• – peroxisomal disorders
• – adrenoleukodystrophy
• – Refsum disease
• – Zellweger syndrome
• – phenylketonurias
• – phenylketonuria, maternal
• – pyruvate carboxylase deficiency disease
• – pyruvate dehydrogenase complex deficiency disease
• – tyrosinemias
• – hepatic encephalopathy
• – kernicterus
• – mitochondrial encephalomyopathies
• – myelinolysis, central pontine
• – Reye syndrome
• – Wernicke encephalopathy

  – [calcium metabolism disorders]

• – calcinosis
• – calciphylaxis
• – CREST syndrome
• – nephrocalcinosis
• – decalcification, pathologic
• – hypercalcemia
• – hypocalcemia
• – tetany
• – osteomalacia
• – pseudohypoparathyroidism
• – pseudopseudohypoparathyroidism
• – rickets

  – [DNA repair-deficiency disorders]

• – ataxia–telangiectasia
• – Bloom syndrome
• – Cockayne syndrome
• – colorectal neoplasms, hereditary nonpolyposis
• – fanconi anemia
• – Li–Fraumeni syndrome
• – Nijmegen breakage syndrome
• – Rothmund–Thomson syndrome
• – severe combined immunodeficiency
• – Werner syndrome
• – xeroderma pigmentosum

  – [dyslipidemias]

• – hyperlipidemia
• – hypercholesterolemia
• – hypercholesterolemia, familial
• – hyperlipidemia, familial combined
• – hypercholesterolemia, familial
• – hyperlipoproteinemia type IV
• – hypertriglyceridemia
• – hyperlipoproteinemia
• – hypercholesterolemia, familial
• – hyperlipoproteinemia type III
• – hyperlipoproteinemia type IV
• – hyperlipoproteinemia type V
• – lipoprotein lipase deficiency, familial
• – hypolipoproteinemia
• – abetalipoproteinemia
• – hypobetalipoproteinemia
• – lecithin acyltransferase deficiency
• – tangier disease

  – [glucose metabolism disorders]

• – diabetes mellitus
• – diabetes mellitus, experimental
• – diabetes mellitus, type 1
• – wolfram syndrome
• – diabetes mellitus, type 2
• – diabetes mellitus, lipoatrophic
• – diabetes, gestational
• – diabetic ketoacidosis
• – prediabetic state
• – glycosuria
• – glycosuria, renal
• – hyperglycemia
• – glucose intolerance
• – hyperinsulinism
• – insulin resistance
• – metabolic syndrome x
• – persistent hyperinsulinemia hypoglycemia of infancy
• – hypoglycemia
• – insulin coma
• – persistent hyperinsulinemia hypoglycemia of infancy

  – [hyperammonemia]

– [hyperamylasemia]

– [hyperbilirubinemia]

• – hyperbilirubinemia, neonatal
• – jaundice, neonatal
• – kernicterus

  – [hyperoxaluria]

• – hyperoxaluria, primary

  – [hyperprolactinemia]

– [hyperuricemia]

– [hypervitaminosis A]

– [iron metabolism disorders]

• – anemia, iron-deficiency
• – iron overload
• – hemochromatosis
• – hemosiderosis

  – [malabsorption syndromes]

• – blind loop syndrome
• – celiac disease
• – lactose intolerance
• – sprue, tropical
• – steatorrhea
• – whipple disease

  – [metabolic syndrome x]

– [metabolism, inborn errors]

• – amino acid metabolism, inborn errors
• – albinism
• – albinism, ocular
• – albinism, oculocutaneous
• – Hermansky–Pudlak syndrome
• – piebaldism
• – alkaptonuria
• – aminoaciduria, renal
• – cystinuria
• – Hartnup disease
• – carbamoyl phosphate synthase I deficiency disease
• – citrullinemia
• – homocystinuria
• – hyperargininemia
• – hyperglycinemia, nonketotic
• – hyperhomocysteinemia
• – hyperlysinemias
• – maple syrup urine disease
• – multiple carboxylase deficiency
• – biotinidase deficiency
• – holocarboxylase synthetase deficiency
• – ornithine carbamoyltransferase deficiency disease
• – phenylketonurias
• – phenylketonuria, maternal
• – tyrosinemias
• – amino acid transport disorders, inborn
• – hartnup disease
• – oculocerebrorenal syndrome
• – amyloidosis, familial
• – amyloid neuropathies, familial
• – cerebral amyloid angiopathy, familial
• – brain diseases, metabolic, inborn
• – abetalipoproteinemia
• – carbamoyl-phosphate synthase i deficiency disease
• – cerebral amyloid angiopathy, familial
• – citrullinemia
• – fucosidosis
• – galactosemias
• – glycogen storage disease type II
• – hartnup disease
• – hepatolenticular degeneration
• – homocystinuria
• – hyperargininemia
• – hyperglycinemia, nonketotic
• – hyperlysinemias
• – Leigh disease
• – Lesch–Nyhan syndrome
• – lysosomal storage diseases, nervous system
• – fucosidosis
• – glycogen storage disease type II
• – mucolipidoses
• – sialic acid storage disease
• – sphingolipidoses
• – Fabry disease
• – gangliosidoses
• – gangliosidoses GM2
• – Sandhoff disease
• – Tay–Sachs disease
• – Tay–Sachs disease, AB variant
• – gangliosidosis gm1
• – Gaucher disease
• – leukodystrophy, globoid cell
• – leukodystrophy, metachromatic
• – Niemann–Pick diseases
• – maple syrup urine disease
• – MELAS syndrome
• – menkes kinky hair syndrome
• – MERRF syndrome
• – mucolipidoses
• – oculocerebrorenal syndrome
• – ornithine carbamoyltransferase deficiency disease
• – peroxisomal disorders
• – adrenoleukodystrophy
• – refsum disease
• – Zellweger syndrome
• – phenylketonurias
• – phenylketonuria, maternal
• – pyruvate carboxylase deficiency disease
• – pyruvate dehydrogenase complex deficiency disease
• – sphingolipidoses
• – Fabry disease
• – gangliosidoses
• – gangliosidoses gm2
• – Sandhoff disease
• – Tay–Sachs disease
• – Tay–Sachs disease, AB variant
• – gangliosidosis gm1
• – Gaucher disease
• – leukodystrophy, globoid cell
• – leukodystrophy, metachromatic
• – Niemann–Pick diseases
• – tyrosinemias
• – carbohydrate metabolism, inborn errors
• – carbohydrate-deficient glycoprotein syndrome
• – fructose metabolism, inborn errors
• – fructose-1,6-diphosphatase deficiency
• – Hereditary fructose intolerance
• – fucosidosis
• – galactosemias
• – glycogen storage disease
• – glycogen storage disease type I
• – glycogen storage disease type II
• – glycogen storage disease type IIb
• – glycogen storage disease type III
• – glycogen storage disease type IV
• – glycogen storage disease type V
• – glycogen storage disease type VI
• – glycogen storage disease type VII
• – glycogen storage disease type VIII
• – hyperoxaluria, primary
• – lactose intolerance
• – mannosidase deficiency diseases
• – alpha-mannosidosis
• – beta-mannosidosis
• – mucolipidoses
• – mucopolysaccharidoses
• – mucopolysaccharidosis I
• – mucopolysaccharidosis II
• – mucopolysaccharidosis III
• – mucopolysaccharidosis IV
• – mucopolysaccharidosis VI
• – mucopolysaccharidosis VII
• – multiple carboxylase deficiency
• – biotinidase deficiency
• – holocarboxylase synthetase deficiency
• – pyruvate metabolism, inborn errors
• – Leigh disease
• – pyruvate carboxylase deficiency disease
• – pyruvate dehydrogenase complex deficiency disease
• – cytochrome-c oxidase deficiency
• – glucosephosphate dehydrogenase deficiency
• – hyperbilirubinemia, hereditary
• – Crigler–Najjar syndrome
• – gilbert disease
• – jaundice, chronic idiopathic
• – lipid metabolism, inborn errors
• – hypercholesterolemia, familial
• – hyperlipidemia, familial combined
• – hypercholesterolemia, familial
• – hyperlipoproteinemia type IV
• – hyperlipoproteinemia type III
• – hyperlipoproteinemia type IV
• – hyperlipoproteinemia type V
• – hypolipoproteinemia
• – abetalipoproteinemia
• – hypobetalipoproteinemia
• – lecithin acyltransferase deficiency
• – Tangier disease
• – lipoidosis
• – cholesterol ester storage disease
• – lipoidproteinosis
• – neuronal ceroid lipofuscinosis
• – Refsum disease
• – Sjögren–Larsson syndrome
• – sphingolipidoses
• – Fabry disease
• – gangliosidoses
• – gangliosidoses GM2
• – Sandhoff disease
• – Tay–Sachs disease
• – Tay–Sachs disease, AB variant
• – gangliosidosis gm1
• – Gaucher disease
• – leukodystrophy, globoid cell
• – leukodystrophy, metachromatic
• – Niemann–Pick diseases
• – sea-blue histiocyte syndrome
• – Wolman disease
• – lipoprotein lipase deficiency, familial
• – peroxisomal disorders
• – acatalasia
• – adrenoleukodystrophy
• – chondrodysplasia punctata, rhizomelic
• – Refsum disease
• – Zellweger syndrome
• – Smith–Lemli–Opitz syndrome
• – xanthomatosis, cerebrotendinous
• – lysosomal storage diseases
• – cholesterol ester storage disease
• – lysosomal storage diseases, nervous system
• – fucosidosis
• – glycogen storage disease type II
• – mucolipidoses
• – sialic acid storage disease
• – sphingolipidoses
• – Fabry disease
• – gangliosidoses
• – gangliosidoses GM2
• – Sandhoff disease
• – Tay–Sachs disease
• – Tay–Sachs disease, AB variant
• – gangliosidosis gm1
• – Gaucher disease
• – leukodystrophy, globoid cell
• – leukodystrophy, metachromatic
• – Niemann–Pick diseases
• – mannosidase deficiency diseases
• – alpha-mannosidosis
• – beta-mannosidosis
• – mucopolysaccharidoses
• – mucopolysaccharidosis I
• – mucopolysaccharidosis II
• – mucopolysaccharidosis III
• – mucopolysaccharidosis IV
• – mucopolysaccharidosis VI
• – mucopolysaccharidosis VII
• – sphingolipidoses
• – Fabry disease
• – gangliosidoses
• – gangliosidoses GM2
• – Sandhoff disease
• – Tay–Sachs disease
• – Tay–Sachs disease, AB variant
• – Gaucher disease
• – leukodystrophy, globoid cell
• – leukodystrophy, metachromatic
• – Niemann–Pick diseases
• – sea-blue histiocyte syndrome
• – Wolman disease
• – metal metabolism, inborn errors
• – hemochromatosis
• – hepatolenticular degeneration
• – hypophosphatasia
• – hypophosphatemia, familial
• – Menkes kinky hair syndrome
• – paralyses, familial periodic
• – hypokalemic periodic paralysis
• – paralysis, hyperkalemic periodic
• – pseudohypoparathyroidism
• – pseudopseudohypoparathyroidism
• – porphyria, erythropoietic
• – porphyrias, hepatic
• – coproporphyria, hereditary
• – porphyria, acute intermittent
• – porphyria cutanea tarda
• – porphyria, hepatoerythropoietic
• – porphyria, variegate
• – protoporphyria, erythropoietic
• – progeria
• – purine–pyrimidine metabolism, inborn errors
• – gout
• – arthritis, gouty
• – Lesch–Nyhan syndrome
• – renal tubular transport, inborn errors
• – acidosis, renal tubular
• – aminoaciduria, renal
• – cystinuria
• – Hartnup disease
• – cystinosis
• – Fanconi syndrome
• – glycosuria, renal
• – hypophosphatemia, familial
• – oculocerebrorenal syndrome
• – pseudohypoaldosteronism
• – steroid metabolism, inborn errors
• – adrenal hyperplasia, congenital
• – mineralocorticoid excess syndrome, apparent
• – ichthyosis, x-linked
• – Smith–Lemli–Opitz syndrome

  – [mitochondrial diseases]

• – cytochrome-c oxidase deficiency
• – Friedreich's ataxia
• – optic atrophy, hereditary, leber
• – Leigh disease
• – mitochondrial myopathies
• – mitochondrial encephalomyopathies
• – MELAS syndrome
• – MERRF syndrome
• – ophthalmoplegia, chronic progressive external
• – Kearns–Sayre syndrome
• – optic atrophy, autosomal dominant
• – pyruvate carboxylase deficiency disease
• – pyruvate dehydrogenase complex deficiency disease

  – [ochronosis]

– [phosphorus metabolism disorders]

• – hypophosphatemia

  – [skin diseases, metabolic]

• – adiposis dolorosa
• – porphyrias
• – porphyria, erythropoietic
• – porphyrias, hepatic
• – coproporphyria, hereditary
• – porphyria, acute intermittent
• – porphyria cutanea tarda
• – porphyria, hepatoerythropoietic
• – porphyria, variegate
• – protoporphyria, erythropoietic
• – xanthogranuloma, juvenile
• – xanthomatosis
• – wolman disease
• – xanthomatosis, cerebrotendinous

  – [wasting syndrome]

• – hiv wasting syndrome

  – [water-electrolyte imbalance]

• – dehydration
• – hypercalcemia
• – hyperkalemia
• – hypernatremia
• – hypocalcemia
• – hypokalemia
• – hyponatremia
• – inappropriate adh syndrome
• – water intoxication

  – [nutrition disorders]

– [child nutrition disorders]

– [infant nutrition disorders]

• – hemorrhagic disease of newborn

  – [malnutrition]

• – deficiency diseases
• – avitaminosis
• – ascorbic acid deficiency
• – scurvy
• – vitamin A deficiency
• – vitamin B deficiency
• – choline deficiency
• – folic acid deficiency
• – pellagra
• – riboflavin deficiency
• – thiamine deficiency
• – beriberi
• – wernicke encephalopathy
• – vitamin B6 deficiency
• – vitamin B12 deficiency
• – anemia, pernicious
• – vitamin D deficiency
• – osteomalacia
• – rickets
• – vitamin E deficiency
• – steatitis
• – vitamin K deficiency
• – hemorrhagic disease of newborn
• – magnesium deficiency
• – potassium deficiency
• – protein deficiency
• – protein-energy malnutrition
• – kwashiorkor
• – swayback
• – fetal nutrition disorders
• – starvation

  – [overnutrition]

• – obesity
• – obesity hypoventilation syndrome
• – obesity, morbid
• – Prader–Willi syndrome

  – [wasting syndrome]

• – hiv wasting syndrome