ICD-10 บท E: โรคต่อใร้ท่อโภชนาการและกระบวนการสร้างและสลาย
จากวิกิพีเดีย สารานุกรมเสรี
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[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
- (E04) Other nontoxic goitre
- (E05) Thyrotoxicosis (hyperthyroidism)
- (E050) Thyrotoxicosis with diffuse goitre
- Graves' disease
- (E050) Thyrotoxicosis with diffuse goitre
- (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
[แก้] (E20-E35) Disorders of other endocrine glands
[แก้] Parathyroid gland / PTH
[แก้] Pituitary gland / ADH, oxytocin, GH, ACTH, TSH, LH, FSH, prolactin
[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
- Congenital adrenal hyperplasia
- (E250) Congenital adrenogenital disorders associated with enzyme deficiency
- (E26) 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
- (E29) Testicular dysfunction
- (E30) Disorders of puberty, not elsewhere classified
[แก้] Other
- (E31) Polyglandular dysfunction
- (E32) Diseases 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
[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
- (E52) Niacin deficiency (pellagra)
- (E53) Deficiency of other 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
- (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
- (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
- (E700) Classical phenylketonuria
- (E701) Other hyperphenylalaninaemias
- (E702) Disorders of tyrosine metabolism
- Alkaptonuria
- Ochronosis
- Tyrosinaemia
- (E703) Albinism
- (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
- (E720) Disorders of amino-acid transport
- (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
- (E740) Glycogen storage disease
- (E75) Disorders of sphingolipid metabolism and other lipid storage disorders
- (E76) Disorders of glycosaminoglycan metabolism
- (E77) Disorders of glycoprotein metabolism
- (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
- (E780) Pure hypercholesterolaemia
- (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
- (E83) Disorders of mineral metabolism
- (E830) Disorders of copper metabolism
- Wilson's disease
- Menkes disease
- (E831) Disorders of iron metabolism
- Hemochromatosis
- (E832) Disorders of zinc metabolism
- (E833) Disorders of phosphorus metabolism
- (E834) Disorders of magnesium metabolism
- Hypermagnesemia
- Hypomagnesemia
- (E835) Disorders of calcium metabolism
- (E830) Disorders of copper metabolism
- (E84) Cystic fibrosis
- (E85) Amyloidosis
- (E850) Non-neuropathic heredofamilial amyloidosis
- Familial Mediterranean fever
- (E850) Non-neuropathic heredofamilial amyloidosis
- (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
- (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
[แก้] ดูเพิ่ม
- รายการอาการในรหัส ICD-10 (List of ICD-10 codes)
- การจำแนกประเภทของโรคตามสถิติและปัญหาสาธารณสุขสัมพันธ์ระหว่างประเทศ (International Statistical Classification of Diseases and Related Health Problems)