ICD-10 บท E: โรคต่อใร้ท่อโภชนาการและกระบวนการสร้างและสลาย

จากวิกิพีเดีย สารานุกรมเสรี

สารบัญ

[แก้] E00-E35 - โรคต่อใร้ท่อ

[แก้] (E00-E07) Disorders of thyroid gland

  • (E00) Congenital iodine-deficiency syndrome
  • (E01) Iodine-deficiency-related thyroid disorders and allied conditions
  • (E02) Subclinical iodine-deficiency hypothyroidism
  • (E03) Other hypothyroidism
    • (E030) Congenital hypothyroidism with diffuse goitre
    • (E031) Congenital hypothyroidism without goitre
    • (E032) Hypothyroidism due to medicaments and other exogenous substances
    • (E033) Postinfectious hypothyroidism
    • (E034) Atrophy of thyroid (acquired)
    • (E035) Myxoedema coma
  • (E04) Other nontoxic goitre
  • (E05) Thyrotoxicosis (hyperthyroidism)
    • (E050) Thyrotoxicosis with diffuse goitre
      • Graves' disease
  • (E06) Thyroiditis
  • (E07) Other disorders of thyroid

[แก้] (E10-E14) Diabetes mellitus

  • Note: the following conditions are subtypes of each code from E10-14:
    • (E1x.0) Diabetic coma
    • (E1x.1) Diabetic ketoacidosis
    • (E1x.2) Diabetic nephropathy
    • (E1x.3) Diabetic retinopathy
    • (E1x.4) Diabetic neuropathy
    • (E1x.5) Diabetic angiopathy
    • (E1x.6) Diabetic arthropathy
  • (E10) Insulin-dependent diabetes mellitus
  • (E11) Non-insulin-dependent diabetes mellitus
  • (E12) Malnutrition-related diabetes mellitus
  • (E13) Other specified diabetes mellitus
  • (E14) Unspecified diabetes mellitus

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

  • (E15) Nondiabetic hypoglycaemic coma
  • (E16) Other disorders of pancreatic internal secretion

[แก้] (E20-E35) Disorders of other endocrine glands

[แก้] Parathyroid gland / PTH

  • (E20) Hypoparathyroidism
    • (E200) Idiopathic hypoparathyroidism
    • (E201) Pseudohypoparathyroidism
  • (E21) Hyperparathyroidism and other disorders of parathyroid gland
    • (E210) Primary hyperparathyroidism
    • (E211) Secondary hyperparathyroidism, not elsewhere classified

[แก้] Pituitary gland / ADH, oxytocin, GH, ACTH, TSH, LH, FSH, prolactin

  • (E22) Hyperfunction of pituitary gland
    • (E220) Acromegaly and pituitary gigantism
    • (E221) Hyperprolactinaemia
    • (E222) Syndrome of inappropriate secretion of antidiuretic hormone
      • Central precocious puberty
  • (E23) Hypofunction and other disorders of pituitary gland
    • (E230) Hypopituitarism
      • Sheehan's syndrome
      • Hypogonadotropic hypogonadism
      • Kallmann syndrome
    • (E231) Drug-induced hypopituitarism
    • (E232) Diabetes insipidus
    • (E233) Hypothalamic dysfunction, not elsewhere classified

[แก้] Adrenal gland / Aldosterone, cortisol, epinephrine, norepinephrine

  • (E24) Cushing's syndrome
  • (E25) Adrenogenital disorders
    • (E250) Congenital adrenogenital disorders associated with enzyme deficiency
      • Congenital adrenal hyperplasia
        • Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
  • (E26) Hyperaldosteronism
    • (E260) Primary hyperaldosteronism
      • Conn's syndrome
    • (E261) Secondary hyperaldosteronism
  • (E27) Other disorders of adrenal gland
    • (E270) Other adrenocortical overactivity
    • (E271) Primary adrenocortical insufficiency
      • Addison's disease
    • (E272) Addisonian crisis
    • (E273) Drug-induced adrenocortical insufficiency
    • (E274) Other and unspecified adrenocortical insufficiency
      • Hypoaldosteronism
      • Adrenocortical insufficiency NOS
    • (E275) Adrenomedullary hyperfunction

[แก้] Gonads / Estrogen, androgens, testosterone

  • (E28) Ovarian dysfunction
    • (E280) Estrogen excess
    • (E281) Androgen excess
    • (E282) Polycystic ovarian syndrome
    • (E283) Primary ovarian failure
      • Premature menopause NOS
  • (E29) Testicular dysfunction
    • (E290) Testicular hyperfunction
    • (E291) Testicular hypofunction
      • 5-Alpha-reductase deficiency (with male pseudohermaphroditism)
      • Testicular hypogonadism NOS
  • (E30) Disorders of puberty, not elsewhere classified
    • (E300) Delayed puberty
    • (E301) Precocious puberty
    • (E308) Other disorders of puberty
      • Premature thelarche

[แก้] Other

  • (E31) Polyglandular dysfunction
    • (E310) Autoimmune polyglandular failure
      • Schmidt's syndrome
    • (E311) Polyglandular hyperfunction
  • (E32) Diseases of thymus
    • (E320) Persistent hyperplasia of thymus
    • (E321) Abscess of thymus
  • (E34) Other endocrine disorders
    • (E340) Carcinoid syndrome
    • (E341) Other hypersecretion of intestinal hormones
    • (E342) Ectopic hormone secretion, not elsewhere classified
    • (E343) Short stature, not elsewhere classified
    • (E344) Constitutional tall stature
    • (E345) Androgen resistance syndrome
      • Reifenstein's syndrome
    • (E348) Other specified endocrine disorders
      • Progeria
  • (E35) Disorders of endocrine glands in diseases classified elsewhere
    • (E350) Disorders of thyroid gland in diseases classified elsewhere
    • (E351) Disorders of adrenal glands in diseases classified elsewhere
    • (E358) Disorders of other endocrine glands in diseases classified elsewhere

[แก้] E40-68 - Nutritional diseases

[แก้] (E40-E46) Malnutrition

  • (E40) Kwashiorkor
  • (E41) Nutritional marasmus
  • (E42) Marasmic kwashiorkor
  • (E43) Unspecified severe protein-energy malnutrition
  • (E44) Protein-energy malnutrition of moderate and mild degree
  • (E45) Retarded development following protein-energy malnutrition
  • (E46) Unspecified protein-energy malnutrition

[แก้] (E50-E64) Other nutritional deficiencies

  • (E50) Vitamin A deficiency
    • (E500) Vitamin A deficiency with conjunctival xerosis
    • (E501) Vitamin A deficiency with Bitot's spot and conjunctival xerosis
    • (E502) Vitamin A deficiency with corneal xerosis
    • (E503) Vitamin A deficiency with corneal ulceration and xerosis
    • (E504) Vitamin A deficiency with keratomalacia
    • (E505) Vitamin A deficiency with night blindness
    • (E506) Vitamin A deficiency with xerophthalmic scars of cornea
    • (E507) Other ocular manifestations of vitamin A deficiency
      • Xerophthalmia NOS
  • (E51) Thiamine deficiency
    • (E511) Beriberi
    • (E512) Wernicke's encephalopathy
  • (E52) Niacin deficiency (pellagra)
  • (E53) Deficiency of other B group vitamins
    • (E530) Riboflavin deficiency
      • Ariboflavinosis
    • (E531) Pyridoxine deficiency
    • (E538) Deficiency of other specified B group vitamins
  • (E54) Ascorbic acid deficiency
    • Scurvy
  • (E55) Vitamin D deficiency
    • (E550) Rickets, active
  • (E56) Other vitamin deficiencies
  • (E58) Dietary calcium deficiency
  • (E59) Dietary selenium deficiency
  • (E60) Dietary zinc deficiency
  • (E61) Deficiency of other nutrient elements
    • (E611) Iron deficiency
    • (E612) Magnesium deficiency
    • (E613) Manganese deficiency
    • (E614) Chromium deficiency
    • (E615) Molybdenum deficiency
    • (E616) Vanadium deficiency
  • (E63) Other nutritional deficiencies
    • (E630) Essential fatty acid (EFA) deficiency
  • (E64) Sequelae of malnutrition and other nutritional deficiencies

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

  • (E65) Localized adiposity
  • (E66) Obesity
  • (E67) Other hyperalimentation
    • (E670) Hypervitaminosis A
    • (E673) Hypervitaminosis D
  • (E68) Sequelae of hyperalimentation

[แก้] E70-E90 - Metabolic diseases

[แก้] (E70-E79) Metabolic disorders of proteins, fats, and carbohydratess

  • (E70) Disorders of aromatic amino-acid metabolism
  • (E71) Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
    • (E710) Maple-syrup-urine disease
    • (E711) Other disorders of branched-chain amino-acid metabolism
      • Propionic acidemia
      • Methylmalonic acidemia
      • Isovaleric acidemia
    • (E712) Disorder of branched-chain amino-acid metabolism, unspecified
    • (E713) Disorders of fatty-acid metabolism
      • Muscle carnitine palmityltransferase deficiency
  • (E72) Other disorders of amino-acid metabolism
    • (E720) Disorders of amino-acid transport
      • Cystinuria
      • Cystinosis
      • Hartnup disease
    • (E721) Disorders of sulfur-bearing amino-acid metabolism
      • Homocystinuria
    • (E722) Disorders of urea cycle metabolism
      • Citrullinaemia
      • Hyperammonemia
    • (E723) Disorders of lysine and hydroxylysine metabolism
      • Glutaric aciduria
    • (E724) Disorders of ornithine metabolism
    • (E725) Disorders of glycine metabolism
  • (E73) Lactose intolerance
  • (E74) Other disorders of carbohydrate metabolism
    • (E740) Glycogen storage disease
      • Glycogen storage disease type I (von Gierke's disease)
      • Glycogen storage disease type II (Pompe's disease)
      • Glycogen storage disease type III
      • Glycogen storage disease type IV
      • Glycogen storage disease type V (McArdle's disease)
    • (E741) Disorders of fructose metabolism
      • Hereditary fructose intolerance
    • (E742) Disorders of galactose metabolism
      • Galactosaemia
  • (E75) Disorders of sphingolipid metabolism and other lipid storage disorders
    • (E750) GM 2 gangliosidosis
    • (E751) Other gangliosidosis
    • (E752) Other sphingolipidosis
      • Gaucher's disease
      • Niemann-Pick disease
    • (E753) Sphingolipidosis, unspecified
    • (E754) Neuronal ceroid lipofuscinosis
      • Batten disease
  • (E76) Disorders of glycosaminoglycan metabolism
    • (E760) Mucopolysaccharidosis, type I
      • Hurler syndrome
    • (E761) Mucopolysaccharidosis, type II
      • Hunter syndrome
    • (E762) Other mucopolysaccharidoses
      • Sanfilippo syndrome
      • Morquio syndrome
  • (E77) Disorders of glycoprotein metabolism
    • (E770) Defects in post-translational modification of lysosomal enzymes
    • (E771) Defects in glycoprotein degradation
  • (E78) Disorders of lipoprotein metabolism and other lipidaemias
    • (E780) Pure hypercholesterolaemia
      • Familial hypercholesterolaemia
      • Familial hypercholesterolaemia
      • Fredrickson's hyperlipoproteinaemia, type IIa
      • Hyperbetalipoproteinaemia
      • Hyperlipidaemia, group A
      • Low-density-lipoprotein-type (LDL) hyperlipoproteinaemia
    • (E781) Pure hyperglyceridaemia
      • Endogenous hyperglyceridaemia
      • Fredrickson's hyperlipoproteinaemia, type IV
      • Hyperlipidaemia, group B
      • Hyperprebetalipoproteinaemia
      • Very-low-density-lipoprotein-type (VLDL) hyperlipoproteinaemia
    • (E782) Mixed hyperlipidaemia
      • Broad- or floating-betalipoproteinaemia
      • Fredrickson's hyperlipoproteinaemia, type IIb or III
      • Hyperbetalipoproteinaemia with prebetalipoproteinaemia
      • Hypercholesterolaemia with endogenous hyperglyceridaemia
      • Hyperlipidaemia, group C
      • Tubero-eruptive xanthoma
      • Xanthoma tuberosum
    • (E783) Hyperchylomicronaemia
      • Fredrickson's hyperlipoproteinaemia, type I or V
      • Hyperlipidaemia, group D
      • Mixed hyperglyceridaemia
    • (E784) Other hyperlipidaemia
      • Familial combined hyperlipidaemia
    • (E785) Hyperlipidaemia, unspecified
    • (E786) Lipoprotein deficiency
  • (E79) Disorders of purine and pyrimidine metabolism
    • (E790) Hyperuricaemia without signs of inflammatory arthritis and tophaceous disease
    • (E791) Lesch-Nyhan syndrome
    • (E798) Other disorders of purine and pyrimidine metabolism
      • Hereditary xanthinuria

[แก้] (E80-E90) Other metabolic disorders

  • (E80) Disorders of porphyrin and bilirubin metabolism
    • (E800) Hereditary erythropoietic porphyria
    • (E801) Porphyria cutanea tarda
    • (E802) Other porphyria
      • Acute intermittent porphyria
    • (E803) Defects of catalase and peroxidase
    • (E804) Gilbert's syndrome
    • (E805) Crigler-Najjar syndrome
  • (E83) Disorders of mineral metabolism
  • (E84) Cystic fibrosis
  • (E85) Amyloidosis
    • (E850) Non-neuropathic heredofamilial amyloidosis
      • Familial Mediterranean fever
  • (E86) Volume depletion
    • Dehydration
    • Hypovolaemia
  • (E87) Other disorders of fluid, electrolyte and acid-base balance
    • (E870) Hyperosmolality and hypernatraemia
    • (E871) Hypo-osmolality and hyponatraemia
    • (E872) Acidosis
      • Respiratory acidosis
      • Metabolic acidosis
      • Lactic acidosis
    • (E873) Alkalosis
    • (E874) Mixed disorder of acid-base balance
    • (E875) Hyperkalaemia
    • (E876) Hypokalaemia
    • (E877) Fluid overload
    • (E878) Other disorders of electrolyte and fluid balance, not elsewhere classified
      • Electrolyte imbalance NOS
      • Hyperchloraemia
      • Hypochloraemia
  • (E88) Other metabolic disorders
    • (E880) Disorders of plasma-protein metabolism, not elsewhere classified
      • Alpha-1-antitrypsin deficiency
    • (E881) Lipodystrophy, not elsewhere classified
    • (E882) Lipomatosis, not elsewhere classified
  • (E89) Postprocedural endocrine and metabolic disorders, not elsewhere classified
    • (E890) Postprocedural hypothyroidism
    • (E891) Postprocedural hypoinsulinaemia
    • (E892) Postprocedural hypoparathyroidism
    • (E893) Postprocedural hypopituitarism
    • (E894) Postprocedural ovarian failure
    • (E895) Postprocedural testicular hypofunction
    • (E896) Postprocedural adrenocortical(-medullary) hypofunction
  • (E90) Nutritional and metabolic disorders in diseases classified elsewhere

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