ICD-10 บท E: โรคต่อใร้ท่อโภชนาการและกระบวนการสร้างและสลาย - วิกิพีเดีย

# ICD-10 บท E: โรคต่อใร้ท่อโภชนาการและกระบวนการสร้างและสลาย

### จากวิกิพีเดีย สารานุกรมเสรี

## [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
  - (E560) Deficiency of vitamin E
  - (E561) Deficiency of vitamin K
- (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
  - (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
- (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
  - (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
- (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

## [แก้] ดูเพิ่ม

- รายการอาการในรหัส ICD-10 (List of ICD-10 codes)
- การจำแนกประเภทของโรคตามสถิติและปัญหาสาธารณสุขสัมพันธ์ระหว่างประเทศ (International Statistical Classification of Diseases and Related Health Problems)

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