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ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases

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Contents

[edit] E00-E35 - Endocrine diseases

[edit] (E00-E07) Thyroid gland / Thyroid hormone

[edit] (E10-E16) Pancreas / Insulin, glucagon

[edit] (E10-E14) Diabetes mellitus

[edit] (E15-E16) Other disorders of glucose regulation and pancreatic internal secretion

[edit] (E20-E21) Parathyroid gland / PTH

[edit] (E22-E23) Pituitary gland / ADH, oxytocin, GH, ACTH, TSH, LH, FSH, prolactin

[edit] (E24-E27) Adrenal gland / Aldosterone, cortisol, epinephrine, norepinephrine

[edit] (E28-E30) Gonads / Estrogen, androgens, testosterone, etc.

[edit] (E31-E35) Other

[edit] E40-68 - Nutritional diseases

[edit] (E40-E46) Malnutrition

[edit] (E50-E64) Other nutritional deficiencies

[edit] (E65-E68) Obesity and other hyperalimentation

[edit] E70-E90 - Metabolic diseases

[edit] (E70-E79) Metabolic disorders of proteins, fats, and carbohydrates

[edit] (E70-E72) Amino-acids

[edit] (E73-E74) Carbohydrates

[edit] (E75) Lipids

[edit] (E76-E78) Combinations

[edit] (E79-E90) Other metabolic disorders

[edit] See also


v·d·e
Endocrine pathology of psychological interest (E00-35)
thyroid Hypothyroidism (Iodine deficiency, Cretinism, Congenital hypothyroidism, Goitre) - Hyperthyroidism (Graves-Basedow disease, Toxic multinodular goitre) - Thyroiditis (De Quervain's thyroiditis, Hashimoto's thyroiditis)

pancreas Diabetes mellitus (type 1, type 2, coma, angiopathy, neuropathy, retinopathy) - Zollinger-Ellison syndrome
parathyroid Hypoparathyroidism - Hyperparathyroidism
pituitary hyperfunction (Acromegaly, Hyperprolactinaemia, ) - Hypopituitarism Kallmann syndrome, Growth hormone deficiency) - Hypothalamic-pituitary dysfunction
adrenal Cushing's syndrome) - Congenital adrenal hyperplasia (due to 21-hydroxylase deficiency) - Bartter syndrome) - Adrenal insufficiency (Addison's disease)
gonads - 5-alpha-reductase deficiency - Hypogonadism - Delayed puberty - Precocious puberty
other - - Psychogenic dwarfism - Androgen insensitivity syndrome -

v·d·e
Nutritional pathology (E40-68, 260-269)
Malnutrition Kwashiorkor - Marasmus
Other underconsumption B vitamins: B1: Beriberi/Wernicke's encephalopathy, B2: Ariboflavinosis, B3: Pellagra, B7: Biotin deficiency, B9: Folate deficiency, B12: Vitamin B12 deficiency

other vitamins: A: Vitamin A deficiency/Bitot's spots, C: Scurvy, D: Rickets/Osteomalacia

mineral: Zinc deficiency - Iron deficiency, Magnesium deficiency - Chromium deficiency

Hyperalimentation Obesity - Hypervitaminosis A - Hypervitaminosis D
Metabolic pathology (E70-90)

amino-acids Phenylketonuria - Alkaptonuria - Ochronosis - Tyrosinemia - Maple syrup urine disease - Propionic acidemia - Methylmalonic acidemia - Isovaleric acidemia - Primary carnitine deficiency - Cystinuria - Cystinosis - Hartnup disease - Homocystinuria - Citrullinemia - Hyperammonemia - Glutaric acidemia type 1
carbohydrates Lactose intolerance - Glycogen storage disease (type I, type II, type III, type IV, type V), Fructose intolerance, Galactosemia
Lipid storage disorders Gangliosidosis - GM2 gangliosidoses (Sandhoff disease, Tay-Sachs disease) - GM1 gangliosidoses - Mucolipidosis type IV - Gaucher's disease - Niemann-Pick disease - Farber disease - Fabry's disease - Metachromatic leukodystrophy - Krabbe disease - Neuronal ceroid lipofuscinosis - Batten disease - Cerebrotendineous xanthomatosis - Wolman disease - Cholesteryl ester storage disease
List of fatty acid metabolism disorders - Hyperlipidemia - Hypercholesterolemia - Familial hypercholesterolemia - Xanthoma - Combined hyperlipidemia - Lecithin cholesterol acyltransferase deficiency - Tangier disease - Abetalipoproteinemia
mineral metabolism Disorders of calcium metabolism - Hypophosphatemia - Hypophosphatasia - Wilson's disease - Menkes disease - Hypermagnesemia - Hypomagnesemia - Hypercalcaemia - Hypocalcaemia
fluid, electrolyte and acid-base balance Electrolyte disturbance - Hypernatremia - Hyponatremia - Respiratory acidosis - Metabolic acidosis - Lactic acidosis - Hypervolemia - Hypokalemia - Hyperkalemia - Mixed disorder of acid-base balance - Hyperchloremia - Hypochloremia - Dehydration
porphyrin and bilirubin Acatalasia - Gilbert's syndrome - Crigler-Najjar syndrome - Dubin-Johnson syndrome - Rotor syndrome - Porphyria (Acute intermittent porphyria, Gunther's disease, Porphyria cutanea tarda, Erythropoietic protoporphyria, Hepatoerythropoietic porphyria, Hereditary coproporphyria, Variegate porphyria)
glycosaminoglycan Mucopolysaccharidosis - Hurler syndrome - Hunter syndrome - Sanfilippo syndrome - Morquio syndrome
glycoprotein I-cell disease - Pseudo-Hurler polydystrophy - Aspartylglucosaminuria - Fucosidosis - Alpha-mannosidosis - Sialidosis
other Alpha 1-antitrypsin deficiency - Cystic fibrosis - Familial Mediterranean fever - Lesch-Nyhan syndrome

ru:МКБ-10: Класс IV
th:ICD-10 บท E: โรคต่อใร้ท่อโภชนาการและกระบวนการสร้างและสลาย
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