code |
description |
Names of diseases (synonyms) |
Review article
|
E70 |
Disturbances in the metabolism of aromatic amino acids |
Phenylketonuria , hyperphenylalaninemia , alkaptonuria , hypertyrosinemia , ochronosis , tyrosinemia , tyrosinosis , albinism , Chediak-Steinbrinck-Higashi syndrome , Cross-McKusick-Breen syndrome , Hermansky-Pudlak syndrome
|
-
|
E71 |
Disturbances in the metabolism of branched amino acids and fatty acid metabolism |
Maple syrup urine disease ( maple syrup urine disease ), Hyperleuzin-Isoleuzinämie , Hypervalinämie , isovaleric , methylmalonic , propionic acidemia , adrenoleukodystrophy ( Addison-signs syndrome ), muscle carnitine palmitoyl transferase deficiency
|
-
|
E72 |
Other disorders of amino acid metabolism |
De-Toni-Debré-Fanconi complex , Hartnup disease , Lowe syndrome , cystinosis , cystinuria , homocystinuria , Methioninämie , Sulfitoxidasemangel , Zystathioninurie , Argininemia , arginine succinic acid disease , hyperammonemia , Citrullinemia , Glutaminazidurie , Hydroxylysinämie , Hyperlysinämie , Ornithinämie , Hyperhydroxyprolinämie , Hyperprolinaemia , non-ketotic hyperglycinaemia , sarcosinemia
|
-
|
E73 |
Lactose intolerance |
Congenital lactase deficiency , secondary lactase deficiency , lactase deficiency , lactose intolerance
|
-
|
E74 |
Other disorders of carbohydrate metabolism |
Glycogen storage disease ( glycogen storage disease ), Andersen's disease , cardiomegalia glycogenica , Cori's disease , Forbes's disease , fructose malabsorption , Hers's disease , Leberphosphorylasemangel , McArdle's disease , phosphofructokinase deficiency , Pompe's disease , Tarui's disease , Glycogen Storage Disease Type I , essential fructosuria , fructose-1,6-diphosphatase deficiency , hereditary fructose intolerance , Galaktokinasemangel , glucose-galactose malabsorption , Saccharasemangel , phosphoenolpyruvate carboxykinase deficiency , pyruvate carboxylase deficiency , pyruvate dehydrogenase deficiency , essential pentosuria , hyperoxaluria ( oxalosis , oxaluria ) Renal glucosuria
|
-
|
E75 |
Disorders of the sphingolipid metabolism and other disorders of lipid storage |
Gangliosidosis , GM1 gangliosidosis , GM2 gangliosidosis , GM3 gangliosidosis , Sandhoff disease , Tay-Sachs disease , sialolipidosis , sphingolipidosis , Fabry-Anderson disease ( Fabry disease ), Farber disease , Gaucher disease , Krabbe disease , metachromatic leukodystrophy , Niemann-Pick disease , sulfatase , Neuronal ceroid lipofuscinosis ( Batten disease ), Batten Kufs syndrome , Bielschowsky Dollinger syndrome , game Meyer-Vogt disease , Wolman's disease , Cerebrotendinous cholesterosis ( van Bogaert-Scherer -Epstein syndrome ) |
-
|
E76 |
Disorders of the glycosaminoglycan metabolism |
Mucopolysaccharidosis , Hurler-Scheie variant , Pfaundler-Hurler disease , Scheie disease , Hunter disease , beta-glucuronidase deficiency , Maroteaux-Lamy disease , Morquio disease , Sanfilippo disease
|
Mucopolysaccharidosis
|
E77 |
Disorders of glycoprotein metabolism |
Mucolipidosis , mucolipidosis II ( I-cell disease ), mucolipidosis III ( pseudo-Hurler polydystrophy ) Aspartylglukosaminurie , Fukosidose , mannosidosis , sialidosis ( mucolipidosis I ) |
-
|
E 78 |
Disorders of lipoprotein metabolism and other lipidemias |
Pure hypercholesterolemia , familial hypercholesterolemia , Hyperbetalipoproteinaemia , hyperlipidemia , hyperlipoproteinemia , pure hypertriglyceridemia , Endogenous hypertriglyceridemia , Hyperpräbetalipoproteinämie , Mixed hyperlipidemia , Tubo-eruptive xanthoma , xanthoma tuberosum , hyperchylomicronaemia , Mixed hypertriglyceridemia , Lipoproteinmangel , A-beta lipoproteinaemia , high-density Lipoproteinmangel , Hypoalphalipoproteinemia , Tangier disease (familial hypoalphalipoproteinemia) , hypobetalipoproteinemia , lecithin cholesterol acyltransferase deficiency , Tangier disease
|
Hypercholesterolemia , hypertriglyceridemia , hyperlipidemia
|
E79 |
Disorders of the purine and pyrimidine metabolism |
Hyperuricemia , Lesch-Nyhan Syndrome , Hereditary Xanthinuria ( Xanthinuria ) |
-
|
E80 |
Disorders of the porphyrin and bilirubin metabolism |
Hereditary erythropoietic porphyria , Congenital erythropoietic porphyria , erythropoietic protoporphyria , porphyria cutanea tarda , Hereditary coproporphyria , acute intermittent porphyria , Akatalasämie ( Takahara syndrome , Akatalasie ), Gilbert's disease syndrome , Crigler-Najjar syndrome , Dubin-Johnson syndrome , Rotor -Syndrome
|
Porphyria
|
E81 E82 |
(not awarded) |
- |
-
|
E83 |
Disorders of mineral metabolism |
Menkes disease , Wilson's disease , hemochromatosis , Acrodermatitis Enteropathica , familial hypophosphatemia , hypophosphatasia , lack of acid phosphatase , vitamin D-resistant osteomalacia , vitamin D-resistant rickets , hypermagnesemia , hypomagnesemia , Family hypokalziurische hypercalcemia , idiopathic hypercalciuria , Hereditary zinc deficiency syndrome
|
-
|
E84 |
Cystic fibrosis |
Cystic fibrosis , cystic fibrosis
|
-
|
E85 |
Amyloidosis |
Heredofamily non-neuropathic amyloidosis , Familial Mediterranean fever , Hereditary amyloid nephropathy , Heredofamily neuropathic amyloidosis , Amyloid polyneuropathy , Secondary systemic amyloidosis , Localized amyloidosis
|
Amyloidosis
|
E86 |
Lack of volume |
Volume depletion , dehydration , hypovolemia
|
-
|
E87 |
Other disorders of the water and electrolyte balance as well as the acid-base balance |
Hyperosmolality , hypernatremia , Hypoosmolalität , hyponatremia , sodium depletion , acidosis , lactic acidosis , metabolic acidosis , respiratory acidosis , alkalosis , metabolic alkalosis , respiratory alkalosis , hyperkalemia , hypokalemia , potassium deficiency , hyperchloraemia , hypochloraemia
|
Electrolyte disorder
|
E88 |
Other metabolic disorders |
Alpha-1 antitrypsin deficiency , bisalbuminemia , lipodystrophy , lipomatosis , lipomatosis dolorosa ( Dercum's disease ), benign symmetrical lipomatosis ( Launois-Bensaude adenolipomatosis ), trimethylaminuria
|
-
|
E89 |
Endocrine and metabolic disorders following medical measures, not elsewhere classified |
Hypothyroidism , hypoinsulinaemia , hyperglycemia , hypoparathyroidism , hypopituitarism , ovarian , testicular hypofunction , adrenal hypofunction , adrenal medulla hypofunction
|
-
|
E90 * |
Nutritional and metabolic disorders in diseases classified elsewhere |
- |
-
|