ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases
This is a shortened version of the fourth chapter of the ICD-10: Endocrine, nutritional and metabolic diseases. It covers ICD codes E00.0 to E90. All versions of the ICD-10, including the most recent one, can be on the website of the World Health Organisation. The ICD-10 can also be downloaded .
Endocrine diseases (E00–E35)
Thyroid gland / Thyroid hormone (E00–E07)
- Congenital iodine-deficiency syndrome
- Iodine-deficiency-related thyroid disorders and allied conditions
- * Iodine-deficiency-related diffuse goitre
- * Iodine-deficiency-related multinodular goitre
- * Iodine-deficiency-related goitre, unspecified
- * Other iodine-deficiency-related thyroid disorders and allied condition
- Subclinical iodine-deficiency hypothyroidism
- Other hypothyroidism
- * Congenital hypothyroidism with diffuse goitre
- * Congenital hypothyroidism without goitre
- * Hypothyroidism due to medicaments and other exogenous substances
- * Postinfectious hypothyroidism
- * Atrophy of thyroid
- * Myxoedema coma
- Other nontoxic goitre
- Thyrotoxicosis
- * Thyrotoxicosis with diffuse goitre
- ** Graves' disease
- * Thyrotoxicosis with toxic single thyroid nodule
- * Thyrotoxicosis with toxic multinodular goitre
- * Thyrotoxicosis from ectopic thyroid tissue
- * Thyrotoxicosis factitia
- * Thyroid crisis or storm
- * Other thyrotoxicosis
- * Thyrotoxicosis, unspecified
- Thyroiditis
- * Acute thyroiditis
- * Subacute thyroiditis
- ** De Quervain's thyroiditis
- * Chronic thyroiditis with thyrotoxicosis
- * Autoimmune thyroiditis
- ** Hashimoto's thyroiditis
- * Drug-induced thyroiditis
- * Other chronic thyroiditis
- ** Riedel's thyroiditis
- * Thyroiditis, unspecified
- Other disorders of thyroid
- * Hypersecretion of calcitonin
- * Dyshormogenetic goitre
- * Other specified disorders of thyroid
- ** Sick-euthyroid syndrome
- * Disorder of thyroid, unspecified
Pancreas / Insulin, glucagon (E10–E16)
Diabetes mellitus (E10–E14)
- Insulin-dependent diabetes mellitus
- * Diabetic coma
- * Diabetic ketoacidosis
- * Diabetic nephropathy
- * Diabetic retinopathy
- * Diabetic neuropathy
- * Diabetic angiopathy
- * Diabetic arthropathy
- Non-insulin-dependent diabetes mellitus
- * Diabetic coma
- * Diabetic ketoacidosis
- * Diabetic nephropathy
- * Diabetic retinopathy
- * Diabetic neuropathy
- * Diabetic angiopathy
- * Diabetic arthropathy
- Malnutrition-related diabetes mellitus
- * Diabetic coma
- * Diabetic ketoacidosis
- * Diabetic nephropathy
- * Diabetic retinopathy
- * Diabetic neuropathy
- * Diabetic angiopathy
- * Diabetic arthropathy
- Other specified diabetes mellitus
- * Diabetic coma
- * Diabetic ketoacidosis
- * Diabetic nephropathy
- * Diabetic retinopathy
- * Diabetic neuropathy
- * Diabetic angiopathy
- * Diabetic arthropathy
- Unspecified diabetes mellitus
- * Diabetic coma
- * Diabetic ketoacidosis
- * Diabetic nephropathy
- * Diabetic retinopathy
- * Diabetic neuropathy
- * Diabetic angiopathy
- * Diabetic arthropathy
Other disorders of glucose regulation and pancreatic internal secretion (E15–E16)
- Nondiabetic hypoglycaemic coma
- ** Drug-induced insulin coma in nondiabetic
- ** Hyperinsulinism with hypoglycaemic coma
- ** Hypoglycaemic coma NOS
- Other disorders of pancreatic internal secretion
- * Drug-induced hypoglycaemia without coma
- * Other hypoglycaemia
- ** Functional nonhyperinsulinaemic hypoglycaemia
- ** Hyperinsulinism: NOS
- ** Hyperinsulinism: functional
- ** Hyperplasia of pancreatic islet beta cells NOS
- ** Posthypoglycaemic coma encephalopathy
- * Hypoglycaemia, unspecified
- * Increased secretion of glucagon
- * Abnormal secretion of gastrin
- ** Hypergastrinaemia
- ** Zollinger-Ellison syndrome
- * Other specified disorders of pancreatic internal secretion
- * Disorder of pancreatic internal secretion, unspecified
Parathyroid gland / PTH (E20–E21)
- Hypoparathyroidism
- * Idiopathic hypoparathyroidism
- * Pseudohypoparathyroidism
- Hyperparathyroidism and other disorders of parathyroid gland
- * Primary hyperparathyroidism
- * Secondary hyperparathyroidism, not elsewhere classified
Pituitary gland / ADH, oxytocin, GH, ACTH, TSH, LH, FSH, prolactin (E22–E23)
- Hyperfunction of pituitary gland
- * Acromegaly and pituitary gigantism
- * Hyperprolactinaemia
- * Syndrome of inappropriate secretion of antidiuretic hormone
- ** Central precocious puberty
- Hypofunction and other disorders of pituitary gland
- * 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
- ** Panhypopituitarism
- ** Pituitary cachexia
- ** Pituitary insufficiency NOS
- ** Pituitary short stature
- ** Sheehan's syndrome
- ** Simmonds' disease
- * Drug-induced hypopituitarism
- * Diabetes insipidus
- * Hypothalamic dysfunction, not elsewhere classified
- * Other disorders of pituitary gland
- ** Abscess of pituitary
- ** Adiposogenital dystrophy
- * Disorder of pituitary gland, unspecified
Adrenal gland / Aldosterone, cortisol, epinephrine, norepinephrine (E24–E27)
- Cushing's syndrome
- * Pituitary-dependent Cushing's disease
- * Nelson's syndrome
- * Ectopic ACTH syndrome
- * Alcohol-induced pseudo-Cushing's syndrome
- * Other Cushing's syndrome
- * Cushing's syndrome, unspecified
- Adrenogenital disorders
- * Congenital adrenogenital disorders associated with enzyme deficiency
- ** Congenital adrenal hyperplasia
- *** Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
- Hyperaldosteronism
- * Primary hyperaldosteronism
- ** Conn's syndrome
- ** Primary aldosteronism due to adrenal hyperplasia
- * Secondary hyperaldosteronism
- * Other hyperaldosteronism
- ** Bartter's syndrome
- * Hyperaldosteronism, unspecified
- Other disorders of adrenal gland
- * Other adrenocortical overactivity
- * Primary adrenocortical insufficiency
- ** Addison's disease
- * Addisonian crisis
- * Drug-induced adrenocortical insufficiency
- * Other and unspecified adrenocortical insufficiency
- ** Hypoaldosteronism
- ** Adrenocortical insufficiency NOS
- * Adrenomedullary hyperfunction
Gonads / Estrogen, androgens, testosterone, etc. (E28–E30)
- Ovarian dysfunction
- * Estrogen excess
- * Androgen excess
- * Polycystic ovarian syndrome
- * Primary ovarian failure
- ** Premature menopause NOS
- Testicular dysfunction
- * Testicular hyperfunction
- * Testicular hypofunction
- ** 5-Alpha-reductase deficiency
- ** Testicular hypogonadism NOS
- Disorders of puberty, not elsewhere classified
- * Delayed puberty
- * Precocious puberty
- * Other disorders of puberty
- ** Premature thelarche
Other (E31–E35)
- Polyglandular dysfunction
- * Autoimmune polyglandular failure
- ** Schmidt's syndrome
- * Polyglandular hyperfunction
- Diseases of thymus
- * Persistent hyperplasia of thymus
- ** Hypertrophy of thymus
- * Abscess of thymus
- Other endocrine disorders
- * Carcinoid syndrome
- * Other hypersecretion of intestinal hormones
- * Ectopic hormone secretion, not elsewhere classified
- * Short stature, not elsewhere classified
- ** NOS
- ** constitutional
- ** Laron-type
- ** psychosocial
- * Constitutional tall stature
- ** Constitutional gigantism
- * Androgen resistance syndrome
- ** Reifenstein's syndrome
- * Other specified endocrine disorders
- ** Progeria
- Disorders of endocrine glands in diseases classified elsewhere
- * Disorders of thyroid gland in diseases classified elsewhere
- * Disorders of adrenal glands in diseases classified elsewhere
- * Disorders of other endocrine glands in diseases classified elsewhere
Nutritional diseases (E40–E68)
Malnutrition (E40–E46)
- Kwashiorkor
- Nutritional marasmus
- Marasmic kwashiorkor
- Unspecified severe protein–energy malnutrition
- Protein–energy malnutrition of moderate and mild degree
- Retarded development following protein–energy malnutrition
- Unspecified protein–energy malnutrition
Other nutritional deficiencies (E50–E64)
- Vitamin A deficiency
- * Vitamin A deficiency with conjunctival xerosis
- * Vitamin A deficiency with Bitot's spot and conjunctival xerosis
- * Vitamin A deficiency with corneal xerosis
- * Vitamin A deficiency with corneal ulceration and xerosis
- * Vitamin A deficiency with keratomalacia
- * Vitamin A deficiency with night blindness
- * Vitamin A deficiency with xerophthalmic scars of cornea
- * Other ocular manifestations of vitamin A deficiency
- ** Xerophthalmia NOS
- Thiamine deficiency
- * Beriberi
- * Wernicke's encephalopathy
- Niacin deficiency
- Deficiency of other B group vitamins
- * Riboflavin deficiency
- ** Ariboflavinosis
- * Pyridoxine deficiency
- * Deficiency of other specified B group vitamins
- Ascorbic acid deficiency
- * Scurvy
- Vitamin D deficiency
- * Rickets, active
- Other vitamin deficiencies
- * Deficiency of vitamin E
- * Deficiency of vitamin K
- Dietary calcium deficiency
- Dietary selenium deficiency
- Dietary zinc deficiency
- Deficiency of other nutrient elements
- * Iron deficiency
- * Magnesium deficiency
- * Manganese deficiency
- * Chromium deficiency
- * Molybdenum deficiency
- * Vanadium deficiency
- Other nutritional deficiencies
- * Essential fatty acid deficiency
- Sequelae of malnutrition and other nutritional deficiencies
Obesity and other hyperalimentation (E65–E68)
- Localized adiposity
- * Fat pad
- Obesity
- * Obesity due to excess calories
- * Drug-induced obesity
- * Extreme obesity with alveolar hypoventilation
- ** Pickwickian syndrome
- * Other obesity
- ** Morbid obesity
- * Obesity, unspecified
- Other hyperalimentation
- * Hypervitaminosis A
- * Hypercarotenaemia
- * Megavitamin-B 6 syndrome
- * Hypervitaminosis D
- Sequelae of hyperalimentation
Metabolic diseases (E70–E90)
Metabolic disorders of proteins, fats, and carbohydrates (E70–E78)
Amino-acids (E70–E72)
- Disorders of aromatic amino-acid metabolism
- * Classical phenylketonuria
- * Other hyperphenylalaninaemias
- * Disorders of tyrosine metabolism
- ** Alkaptonuria
- ** Ochronosis
- ** Tyrosinaemia
- * Albinism
- ** Oculocutaneous albinism
- ** Partial albinism
- ** Oculocutaneous albinism type 1
- ** Oculocutaneous albinism type 2
- ** Albinoidism
- ** Waardenburg syndrome
- ** Chédiak–Higashi syndrome
- ** Piebaldism
- ** Tietz syndrome
- ** Hermansky–Pudlak syndrome
- ** Cross syndrome
- * Other disorders of aromatic amino-acid metabolism
- ** Disorders of histidine metabolism
- ** Disorders of tryptophan metabolism
- * Disorder of aromatic amino-acid metabolism, unspecified
- Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
- * Maple-syrup-urine disease
- * Other disorders of branched-chain amino-acid metabolism
- ** Propionic acidemia
- ** Methylmalonic acidemia
- ** Isovaleric acidemia
- * Disorder of branched-chain amino-acid metabolism, unspecified
- * Disorders of fatty-acid metabolism
- ** Adrenoleukodystrophy
- ** Muscle carnitine palmityltransferase deficiency
- Other disorders of amino-acid metabolism
- * Disorders of amino-acid transport
- ** Cystinuria
- ** Cystinosis
- ** Hartnup disease
- ** Lowe's syndrome
- * Disorders of sulfur-bearing amino-acid metabolism
- ** Cystathioninuria
- ** Homocystinuria
- ** Methioninaemia
- ** Sulfite oxidase deficiency
- * Disorders of urea cycle metabolism
- ** Argininaemia
- ** Argininosuccinic aciduria
- ** Citrullinaemia
- ** Hyperammonaemia
- * Disorders of lysine and hydroxylysine metabolism
- ** Glutaric aciduria
- ** Hydroxylysinaemia
- ** Hyperlysinaemia
- ** Lysinuric protein intolerance
- * Disorders of ornithine metabolism
- ** Ornithinaemia
- * Disorders of glycine metabolism
- ** Hyperhydroxyprolinaemia
- ** Hyperprolinaemia
- ** Non-ketotic hyperglycinaemia
- ** Sarcosinaemia
Carbohydrates (E73–E74)
- Lactose intolerance
- Other disorders of carbohydrate metabolism
- * Glycogen storage disease
- ** Glycogen storage disease type I
- ** Glycogen storage disease type II
- ** Glycogen storage disease type III
- ** Glycogen storage disease type IV
- ** Glycogen storage disease type V
- * Disorders of fructose metabolism
- ** Essential fructosuria
- ** Fructose-1,6-diphosphatase deficiency
- ** Hereditary fructose intolerance
- * Disorders of galactose metabolism
- ** Galactosaemia
- ** Galactokinase deficiency
- * Other disorders of intestinal carbohydrate absorption
- ** Glucose-galactose malabsorption
- ** Sucrase deficiency
- * Disorders of pyruvate metabolism and gluconeogenesis
- ** Deficiency of phosphoenolpyruvate carboxykinase
- ** Deficiency of pyruvate carboxylase
- ** Deficiency of pyruvate dehydrogenase
- * Other specified disorders of carbohydrate metabolism
- ** Essential pentosuria
- ** Oxalosis
- ** Oxaluria
- ** Renal glycosuria
- * Disorder of carbohydrate metabolism, unspecified
Lipids (E75)
- Disorders of sphingolipid metabolism and other lipid storage disorders
- * GM 2 gangliosidosis
- ** Sandhoff disease
- ** Tay–Sachs disease
- * Other gangliosidosis
- ** GM 1
- ** GM 3
- ** Mucolipidosis type IV
- * Other sphingolipidosis
- ** Gaucher's disease
- ** Niemann–Pick disease
- **Farber disease
- **Fabry disease
- * Sphingolipidosis, unspecified
- * Neuronal ceroid lipofuscinosis
- ** Batten disease
- ** Jansky–Bielschowsky disease
- ** Kufs disease
- ** Spielmeyer–Vogt disease
- * Other lipid storage disorders
- ** Cerebrotendinous cholesterosis
- ** Wolman's disease
- * Lipid storage disorder, unspecified
Combinations (E76–E78)
- Disorders of glycosaminoglycan metabolism
- * Mucopolysaccharidosis, type I
- ** Hurler syndrome
- * Mucopolysaccharidosis, type II
- ** Hunter syndrome
- * Other mucopolysaccharidoses
- ** Sanfilippo syndrome
- ** Morquio syndrome
- Disorders of glycoprotein metabolism
- * Defects in post-translational modification of lysosomal enzymes
- ** Mucolipidosis II
- ** Mucolipidosis III
- * Defects in glycoprotein degradation
- ** Aspartylglucosaminuria
- ** Fucosidosis
- ** Mannosidosis
- ** Sialidosis
- * Other disorders of glycoprotein metabolism
- * Disorder of glycoprotein metabolism, unspecified
- Disorders of lipoprotein metabolism and other lipidaemias
- * Pure hypercholesterolaemia
- ** Familial hypercholesterolaemia
- ** Fredrickson's hyperlipoproteinaemia, type IIa
- ** Hyperbetalipoproteinaemia
- ** Hyperlipidaemia, group A
- ** Low-density-lipoprotein-type hyperlipoproteinaemia
- * Pure hyperglyceridaemia
- ** Endogenous hyperglyceridaemia
- ** Fredrickson's hyperlipoproteinaemia, type IV
- ** Hyperlipidaemia, group B
- ** Hyperprebetalipoproteinaemia
- ** Very-low-density-lipoprotein-type hyperlipoproteinaemia
- * 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
- * Hyperchylomicronaemia
- ** Fredrickson's hyperlipoproteinaemia, type I or V
- ** Hyperlipidaemia, group D
- ** Mixed hyperglyceridaemia
- * Other hyperlipidaemia
- ** Familial combined hyperlipidaemia
- * Hyperlipidaemia, unspecified
- * Lipoprotein deficiency
- ** Abetalipoproteinaemia
- ** High-density lipoprotein deficiency
- ** Hypoalphalipoproteinaemia
- ** Hypobetalipoproteinaemia
- ** Lecithin cholesterol acyltransferase deficiency
- ** Tangier disease
Other metabolic disorders (E79–E90)
- Disorders of purine and pyrimidine metabolism
- * Hyperuricaemia without signs of inflammatory arthritis and tophaceous disease
- * Lesch–Nyhan syndrome
- * Other disorders of purine and pyrimidine metabolism
- ** Hereditary xanthinuria
- Disorders of porphyrin and bilirubin metabolism
- * Hereditary erythropoietic porphyria
- ** Erythropoietic protoporphyria
- ** Erythropoietic porphyria, congenital
- ** Gunther disease
- ** Erythropoietic porphyria
- ** Erythropoietic coproporphyria
- * Porphyria cutanea tarda
- ** Sporadic porphyria cutanea tarda
- ** Familial porphyria cutanea tarda
- * Other porphyria
- ** Acute intermittent porphyria
- ** Hereditary coproporphyria
- ** Variegate porphyria
- ** Chester porphyria
- ** Porphyria, hepatic
- ** Pseudoporphyria
- ** Toxic porphyria
- ** Hepatoerythropoietic porphyria
- ** Porphyria, NOS
- * Defects of catalase and peroxidase
- ** Acatalasia
- * Gilbert's syndrome
- * Crigler–Najjar syndrome
- * Other disorders of bilirubin metabolism
- ** Dubin–Johnson syndrome
- ** Rotor syndrome
- * Disorder of bilirubin metabolism, unspecified
- Disorders of mineral metabolism
- * Disorders of copper metabolism
- ** Wilson's disease
- ** Menkes disease
- * Disorders of iron metabolism
- ** Aceruloplasminemia
- ** Hemochromatosis
- * Disorders of zinc metabolism
- ** Acrodermatitis enteropathica
- * Disorders of phosphorus metabolism
- ** Acid phosphatase deficiency
- ** Familial hypophosphataemia
- ** Hypophosphatasia
- ** Vitamin-D-resistant osteomalacia
- ** Vitamin-D-resistant rickets
- * Disorders of magnesium metabolism
- ** Hypermagnesemia
- ** Hypomagnesemia
- * Disorders of calcium metabolism
- ** Familial hypocalciuric hypercalcaemia
- ** Idiopathic hypercalciuria
- Cystic fibrosis
- Amyloidosis
- * Non-neuropathic heredofamilial amyloidosis
- ** Familial Mediterranean fever
- ** Hereditary amyloid nephropathy
- * Neuropathic heredofamilial amyloidosis
- ** Amyloid polyneuropathy
- * Heredofamilial amyloidosis, unspecified
- * Secondary systemic amyloidosis
- ** Haemodialysis-associated amyloidosis
- * Organ-limited amyloidosis
- ** Localized amyloidosis
- * Other amyloidosis
- * Amyloidosis, unspecified
- Volume depletion
- * Dehydration
- * Hypovolaemia
- Other disorders of fluid, electrolyte and acid–base balance
- * Hyperosmolality and hypernatraemia
- * Hypo-osmolality and hyponatraemia
- * Acidosis
- ** Respiratory acidosis
- ** Metabolic acidosis
- ** Lactic acidosis
- * Alkalosis
- * Mixed disorder of acid–base balance
- * Hyperkalaemia
- * Hypokalaemia
- * Fluid overload
- * Other disorders of electrolyte and fluid balance, not elsewhere classified
- ** Electrolyte imbalance NOS
- ** Hyperchloraemia
- ** Hypochloraemia
- Other metabolic disorders
- * Disorders of plasma-protein metabolism, not elsewhere classified
- ** Alpha-1-antitrypsin deficiency
- ** Bisalbuminaemia
- * Lipodystrophy, not elsewhere classified
- * Lipomatosis, not elsewhere classified
- * Other specified metabolic disorders
- ** Launois–Bensaude adenolipomatosis
- ** Trimethylaminuria
- * Metabolic disorder, unspecified
- Postprocedural endocrine and metabolic disorders, not elsewhere classified
- * Postprocedural hypothyroidism
- * Postprocedural hypoinsulinaemia
- * Postprocedural hypoparathyroidism
- * Postprocedural hypopituitarism
- * Postprocedural ovarian failure
- * Postprocedural testicular hypofunction
- * Postprocedural adrenocortical hypofunction
- Nutritional and metabolic disorders in diseases classified elsewhere
Excludes
- Autoimmune disease NOS
- Certain conditions originating in the perinatal period
- Complications of pregnancy, childbirth and the puerperium
- Congenital malformations, deformations and chromosomal abnormalities
- Human immunodeficiency virus disease
- Injury, poisoning and certain other consequences of external causes
- Neoplasms
- Symptoms, signs, and abnormal clinical and laboratory findings, NEC