ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
E00-E35 - Endocrine diseases
(E00-E07) Thyroid gland / Thyroid hormone
- (E01) Iodine-deficiency-related thyroid disorders and allied conditions
- (E01.0) Iodine-deficiency-related diffuse (endemic) goitre
- (E01.1) Iodine-deficiency-related multinodular (endemic) goitre
- (E01.2) Iodine-deficiency-related (endemic) goitre, unspecified
- (E01.8) Other iodine-deficiency-related thyroid disorders and allied condition
- (E02) Subclinical iodine-deficiency hypothyroidism
- (E03) Other hypothyroidism
- (E03.0) Congenital hypothyroidism with diffuse goitre
- (E03.1) Congenital hypothyroidism without goitre
- (E03.2) Hypothyroidism due to medicaments and other exogenous substances
- (E03.3) Postinfectious hypothyroidism
- (E03.4) Atrophy of thyroid (acquired)
- (E03.5) Myxoedema coma
- (E04) Other nontoxic goitre
- (E05) Thyrotoxicosis (hyperthyroidism)
- (E05.0) Thyrotoxicosis with diffuse goitre
- (E05.1) Thyrotoxicosis with toxic single thyroid nodule
- (E05.2) Thyrotoxicosis with toxic multinodular goitre
- (E05.3) Thyrotoxicosis from ectopic thyroid tissue
- (E05.4) Thyrotoxicosis factitia
- (E05.5) Thyroid crisis or storm
- (E05.8) Other thyrotoxicosis
- (E05.9) Thyrotoxicosis, unspecified
- (E06) Thyroiditis
- (E06.0) Acute thyroiditis
- (E06.1) Subacute thyroiditis
- (E06.2) Chronic thyroiditis with transient thyrotoxicosis
- (E06.3) Autoimmune thyroiditis
- (E06.4) Drug-induced thyroiditis
- (E06.5) Other chronic thyroiditis
- (E06.9) Thyroiditis, unspecified
(E10-E16) Pancreas / Insulin, glucagon
(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
(E15-E16) Other disorders of glucose regulation and pancreatic internal secretion
- (E15) Nondiabetic hypoglycaemic coma
- Drug-induced insulin coma in nondiabetic
- Hyperinsulinism with hypoglycaemic coma
- Hypoglycaemic com NOS
- (E16) Other disorders of pancreatic internal secretion
- (E16.0) Drug-induced hypoglycaemia without coma
- (E16.1) Other hypoglycaemia
- Functional nonhyperinsulinaemic hypoglycaemia
- Hyperinsulinism: NOS
- Hyperinsulinism: functional
- Hyperplasia of pancreatic islet beta cells NOS
- Posthypoglycaemic coma encephalopathy
- (E16.2) Hypoglycaemia, unspecified
- (E16.3) Increased secretion of glucagon
- (E16.4) Abnormal secretion of gastrin
- Hypergastrinaemia
- Zollinger-Ellison syndrome
- (E16.8) Other specified disorders of pancreatic internal secretion
- (E16.9) Disorder of pancreatic internal secretion, unspecified
(E20-E21) Parathyroid gland / PTH
- (E21) Hyperparathyroidism and other disorders of parathyroid gland
- (E21.0) Primary hyperparathyroidism
- (E21.1) Secondary hyperparathyroidism, not elsewhere classified
(E22-E23) Pituitary gland / ADH, oxytocin, GH, ACTH, TSH, LH, FSH, prolactin
- (E22) Hyperfunction of pituitary gland
- (E23) Hypofunction and other disorders of pituitary gland
- (E23.0) Hypopituitarism
- Fertile eunuch syndrome
- Hypogonadotropic hypogonadism
- Idiopathic growth hormone deficiency
- Isolated deficiency of gonadotropin
- Isolated deficiency of growth hormone
- Isolated deficiency of pituitary hormone
- Kallmann's syndrome
- Lorain-Levi short stature
- Necrosis of pituitary gland (postpartum)
- Panhypopituitarism
- Pituitary cachexia
- Pituitary insufficiency NOS
- Pituitary short stature
- Sheehan's syndrome
- Simmonds' disease
- (E23.0) Hypopituitarism
- (E23.1) Drug-induced hypopituitarism
- (E23.2) Diabetes insipidus
- (E23.3) Hypothalamic dysfunction, not elsewhere classified
(E24-E27) Adrenal gland / Aldosterone, cortisol, epinephrine, norepinephrine
- (E24) Cushing's syndrome
- (E24.0) Pituitary-dependent Cushing's disease
- (E24.1) Nelson's syndrome
- (E24.2) Ectopic ACTH syndrome
- (E24.3) Alcohol-induced pseudo-Cushing's syndrome
- (E24.4) Other Cushing's syndrome
- (E24.5) Cushing's syndrome, unspecified
- (E25) Adrenogenital disorders
- (E25.0) Congenital adrenogenital disorders associated with enzyme deficiency
- (E26) Hyperaldosteronism
- (E26.0) Primary hyperaldosteronism
- Conn's syndrome
- Primary aldosteronism due to adrenal hyperplasia (bilateral)
- (E26.1) Secondary hyperaldosteronism
- (E26.8) Other hyperaldosteronism
- (E26.9) Hyperaldosteronism, unspecified
- (E26.0) Primary hyperaldosteronism
- (E27) Other disorders of adrenal gland
- (E27.0) Other adrenocortical overactivity
- (E27.1) Primary adrenocortical insufficiency
- (E27.2) Addisonian crisis
- (E27.3) Drug-induced adrenocortical insufficiency
- (E27.4) Other and unspecified adrenocortical insufficiency
- (E27.5) Adrenomedullary hyperfunction
(E28-E30) Gonads / Estrogen, androgens, testosterone, etc.
- (E28) Ovarian dysfunction
- (E28.0) Estrogen excess
- (E28.1) Androgen excess
- (E28.2) Polycystic ovarian syndrome
- (E28.3) Primary ovarian failure
- (E29) Testicular dysfunction
- (E29.0) Testicular hyperfunction
- (E29.1) Testicular hypofunction
- 5-Alpha-reductase deficiency (with male pseudohermaphroditism)
- Testicular hypogonadism NOS
- (E30) Disorders of puberty, not elsewhere classified
- (E30.0) Delayed puberty
- (E30.1) Precocious puberty
- (E30.8) Other disorders of puberty
- Premature thelarche
(E31-E35) Other
- (E31) Polyglandular dysfunction
- (E31.0) Autoimmune polyglandular failure
- (E31.1) Polyglandular hyperfunction
- (E34) Other endocrine disorders
- (E34.0) Carcinoid syndrome
- (E34.1) Other hypersecretion of intestinal hormones
- (E34.2) Ectopic hormone secretion, not elsewhere classified
- (E34.3) Short stature, not elsewhere classified
- NOS
- constitutional
- Laron-type
- psychosocial
- (E34.4) Constitutional tall stature
- (E34.5) Androgen resistance syndrome
- (E34.8) Other specified endocrine disorders
- (E35) Disorders of endocrine glands in diseases classified elsewhere
- (E35.0) Disorders of thyroid gland in diseases classified elsewhere
- (E35.1) Disorders of adrenal glands in diseases classified elsewhere
- (E35.8) Disorders of other endocrine glands in diseases classified elsewhere
E40-68 - Nutritional diseases
(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
(E50-E64) Other nutritional deficiencies
- (E50) Vitamin A deficiency
- (E50.0) Vitamin A deficiency with conjunctival xerosis
- (E50.1) Vitamin A deficiency with Bitot's spot and conjunctival xerosis
- (E50.2) Vitamin A deficiency with corneal xerosis
- (E50.3) Vitamin A deficiency with corneal ulceration and xerosis
- (E50.4) Vitamin A deficiency with keratomalacia
- (E50.5) Vitamin A deficiency with night blindness
- (E50.6) Vitamin A deficiency with xerophthalmic scars of cornea
- (E50.7) Other ocular manifestations of vitamin A deficiency
- Xerophthalmia NOS
- (E51) Thiamine deficiency
- (E52) Niacin deficiency (pellagra)
- (E53) Deficiency of other B group vitamins
- (E53.0) Riboflavin deficiency
- (E53.1) Pyridoxine deficiency
- (E53.8) Deficiency of other specified B group vitamins
- (E54) Ascorbic acid deficiency
- (E55) Vitamin D deficiency
- (E56) Other vitamin deficiencies
- (E58) Dietary calcium deficiency
- (E59) Dietary selenium deficiency
- (E60) Dietary zinc deficiency
- (E61) Deficiency of other nutrient elements
- (E61.1) Iron deficiency
- (E61.2) Magnesium deficiency
- (E61.3) Manganese deficiency
- (E61.4) Chromium deficiency
- (E61.5) Molybdenum deficiency
- (E61.6) Vanadium deficiency
- (E63) Other nutritional deficiencies
- (E63.0) Essential fatty acid (EFA) deficiency
- (E64) Sequelae of malnutrition and other nutritional deficiencies
(E65-E68) Obesity and other hyperalimentation
- (E66) Obesity
- (E67) Other hyperalimentation
- (E67.0) Hypervitaminosis A
- (E67.1) Hypercarotenaemia
- (E67.2) Megavitamin-B 6 syndrome
- (E67.3) Hypervitaminosis D
- (E68) Sequelae of hyperalimentation
E70-E90 - Metabolic diseases
(E70-E79) Metabolic disorders of proteins, fats, and carbohydrates
(E70-E72) Amino-acids
- (E70) Disorders of aromatic amino-acid metabolism
- (E70.0) Classical phenylketonuria
- (E70.1) Other hyperphenylalaninaemias
- (E70.2) Disorders of tyrosine metabolism
- Alkaptonuria (ILDS E70.210)
- Ochronosis (ILDS E70.230)
- Tyrosinaemia
- (E70.3) Albinism
- Chediak-Higashi syndrome
- Cross syndrome
- Hermansky-Pudlak syndrome
- (E70.8) Other disorders of aromatic amino-acid metabolism
- Disorders of histidine metabolism
- Disorders of tryptophan metabolism
- (E70.9) Disorder of aromatic amino-acid metabolism, unspecified
- (E71) Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
- (E71.0) Maple-syrup-urine disease
- (E71.1) Other disorders of branched-chain amino-acid metabolism
- (E71.2) Disorder of branched-chain amino-acid metabolism, unspecified
- (E71.3) Disorders of fatty-acid metabolism
- Adrenoleukodystrophy (Addison-Schilder)
- Muscle carnitine palmityltransferase deficiency
- (E72) Other disorders of amino-acid metabolism
- (E72.0) Disorders of amino-acid transport
- (E72.1) Disorders of sulfur-bearing amino-acid metabolism
- Cystathioninuria
- Homocystinuria
- Methioninaemia
- Sulfite oxidase deficiency
- (E72.2) Disorders of urea cycle metabolism
- Argininaemia
- Argininosuccinic aciduria
- Citrullinaemia
- Hyperammonaemia
- (E72.3) Disorders of lysine and hydroxylysine metabolism
- Glutaric aciduria
- Hydroxylysinaemia
- Hyperlysinaemia
- (E72.4) Disorders of ornithine metabolism
- Ornithinaemia (types I, II)
- (E72.5) Disorders of glycine metabolism
- Hyperhydroxyprolinaemia
- Hyperprolinaemia (types I, II)
- Non-ketotic hyperglycinaemia
- Sarcosinaemia
(E73-E74) Carbohydrates
- (E74) Other disorders of carbohydrate metabolism
- (E74.0) Glycogen storage disease
- (E74.1) Disorders of fructose metabolism
- (E74.2) Disorders of galactose metabolism
- (E74.3) Other disorders of intestinal carbohydrate absorption
- (E74.4) Disorders of pyruvate metabolism and gluconeogenesis
- (E74.8) Other specified disorders of carbohydrate metabolism
- Essential pentosuria
- Oxalosis
- Oxaluria
- Renal glycosuria
- (E74.9) Disorder of carbohydrate metabolism, unspecified
(E75) Lipids
- (E75) Disorders of sphingolipid metabolism and other lipid storage disorders
- (E75.0) GM 2 gangliosidosis
- (E75.1) Other gangliosidosis
- GM 1
- GM 3
- Mucolipidosis IV
- (E75.2) Other sphingolipidosis
- Gaucher's disease (ILDS E75.220)
- Niemann-Pick disease (ILDS E75.230)
- Farber's disease (ILDS E75.240)
- Fabry's disease (ILDS E75.250)
- (E75.3) Sphingolipidosis, unspecified
- (E75.4) Neuronal ceroid lipofuscinosis
- Batten disease (Type 3)
- Bielschowsky-Jansky disease (Type 2)
- Kufs disease (Type 4)
- Spielmeyer-Vogt disease (Type 3)
- (E75.5) Other lipid storage disorders
- Cerebrotendinous cholesterosis (van Bogaert-Scherer-Epstein)
- Wolman's disease
- (E75.6) Lipid storage disorder, unspecified
(E76-E78) Combinations
- (E76) Disorders of glycosaminoglycan metabolism
- (E76.0) Mucopolysaccharidosis, type I
- (E76.1) Mucopolysaccharidosis, type II
- (E76.2) Other mucopolysaccharidoses
- (E77) Disorders of glycoprotein metabolism
- (E77.0) Defects in post-translational modification of lysosomal enzymes
- (E77.1) Defects in glycoprotein degradation
- (E78) Disorders of lipoprotein metabolism and other lipidaemias
- (E78.0) Pure hypercholesterolaemia
- Familial hypercholesterolaemia
- Fredrickson's hyperlipoproteinaemia, type IIa
- Hyperbetalipoproteinaemia
- Hyperlipidaemia, group A
- Low-density-lipoprotein-type (LDL) hyperlipoproteinaemia
- (E78.1) Pure hyperglyceridaemia
- Endogenous hyperglyceridaemia
- Fredrickson's hyperlipoproteinaemia, type IV
- Hyperlipidaemia, group B
- Hyperprebetalipoproteinaemia
- Very-low-density-lipoprotein-type (VLDL) hyperlipoproteinaemia
- (E78.2) 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
- (E78.3) Hyperchylomicronaemia
- Fredrickson's hyperlipoproteinaemia, type I or V
- Hyperlipidaemia, group D
- Mixed hyperglyceridaemia
- (E78.4) Other hyperlipidaemia
- (E78.5) Hyperlipidaemia, unspecified
- (E78.6) Lipoprotein deficiency
- Abetalipoproteinaemia
- High-density lipoprotein deficiency
- Hypoalphalipoproteinaemia
- Hypobetalipoproteinaemia (familial)
- Lecithin cholesterol acyltransferase deficiency
- Tangier disease
- (E78.0) Pure hypercholesterolaemia
(E79-E90) Other metabolic disorders
- (E79) Disorders of purine and pyrimidine metabolism
- (E79.0) Hyperuricaemia without signs of inflammatory arthritis and tophaceous disease
- (E79.1) Lesch-Nyhan syndrome
- (E79.8) Other disorders of purine and pyrimidine metabolism
- Hereditary xanthinuria
- (E80) Disorders of porphyrin and bilirubin metabolism
- (E80.0) Hereditary erythropoietic porphyria
- Erythropoietic protoporphyria (ILDS E80.010)
- Erythropoietic porphyria, congenital (ILDS E80.020)
- Gunther's disease (ILDS (ILDS E80.020)
- Erythropoietic porphyria (ILDS (ILDS E80.030)
- Erythropoietic coproporphyria (ILDS E80.040)
- (E80.1) Porphyria cutanea tarda
- (E80.2) Other porphyria
- Acute intermittent porphyria (ILDS E80.210)
- Hereditary coproporphyria (ILDS E80.222)
- Variegate porphyria (ILDS E80.230)
- Chester porphyria (ILDS E80.232)
- Porphyria, hepatic (ILDS E80.240)
- Pseudoporphyria (ILDS E80.250)
- Toxic porphyria (ILDS E80.260)
- Hepatoerythropoietic porphyria (ILDS E80.282)
- Porphyria, NOS (ILDS E80.290)
- (E80.3) Defects of catalase and peroxidase
- Acatalasia (Takahara)
- (E80.4) Gilbert's syndrome
- (E80.5) Crigler-Najjar syndrome
- (E80.6) Other disorders of bilirubin metabolism
- (E80.7) Disorder of bilirubin metabolism, unspecified
- (E80.0) Hereditary erythropoietic porphyria
- (E83) Disorders of mineral metabolism
- (E83.0) Disorders of copper metabolism
- (E83.1) Disorders of iron metabolism
- (E83.2) Disorders of zinc metabolism
- (E83.3) Disorders of phosphorus metabolism
- Acid phosphatase deficiency
- Familial hypophosphataemia
- Hypophosphatasia
- Vitamin-D-resistant osteomalacia
- Vitamin-D-resistant rickets
- (E83.4) Disorders of magnesium metabolism
- (E83.5) Disorders of calcium metabolism
- Familial hypocalciuric hypercalcaemia
- Idiopathic hypercalciuria
- (E87) Other disorders of fluid, electrolyte and acid-base balance
- (E87.0) Hyperosmolality and hypernatraemia
- (E87.1) Hypo-osmolality and hyponatraemia
- (E87.2) Acidosis
- (E87.3) Alkalosis
- (E87.4) Mixed disorder of acid-base balance
- (E87.5) Hyperkalaemia
- (E87.6) Hypokalaemia
- (E87.7) Fluid overload
- (E87.8) Other disorders of electrolyte and fluid balance, not elsewhere classified
- (E88) Other metabolic disorders
- (E88.0) Disorders of plasma-protein metabolism, not elsewhere classified
- (E88.1) Lipodystrophy, not elsewhere classified
- (E88.2) Lipomatosis, not elsewhere classified
- (E89) Postprocedural endocrine and metabolic disorders, not elsewhere classified
- (E89.0) Postprocedural hypothyroidism
- (E89.1) Postprocedural hypoinsulinaemia
- (E89.2) Postprocedural hypoparathyroidism
- (E89.3) Postprocedural hypopituitarism
- (E89.4) Postprocedural ovarian failure
- (E89.5) Postprocedural testicular hypofunction
- (E89.6) Postprocedural adrenocortical(-medullary) hypofunction
- (E90) Nutritional and metabolic disorders in diseases classified elsewhere
See also
- List of ICD-10 codes
- International Statistical Classification of Diseases and Related Health Problems
- List of ICD-9 codes 240-279: Endocrine, nutritional and metabolic diseases, and immunity disorders
Template:Nutritional pathology Template:Endocrine, nutritional and metabolic pathology
nl:ICD10 Hoofdstuk IV
th:ICD-10 บท E: โรคต่อใร้ท่อโภชนาการและกระบวนการสร้างและสลาย