ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases

ICD-10 chapters

Chapter	Block	Title
I	A00–B99	Certain infectious and parasitic diseases
II	C00–D48	Neoplasms
III	D50–D89	Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
IV	E00–E90	Endocrine, nutritional and metabolic diseases
V	F00–F99	Mental and behavioural disorders
VI	G00–G99	Diseases of the nervous system
VII	H00–H59	Diseases of the eye and adnexa
VIII	H60–H95	Diseases of the ear and mastoid process
IX	I00–I99	Diseases of the circulatory system
X	J00–J99	Diseases of the respiratory system
XI	K00–K93	Diseases of the digestive system
XII	L00–L99	Diseases of the skin and subcutaneous tissue
XIII	M00–M99	Diseases of the musculoskeletal system and connective tissue
XIV	N00–N99	Diseases of the genitourinary system
XV	O00–O99	Pregnancy, childbirth and the puerperium
XVI	P00–P96	Certain conditions originating in the perinatal period
XVII	Q00–Q99	Congenital malformations, deformations and chromosomal abnormalities
XVIII	R00–R99	Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified
XIX	S00–T98	Injury, poisoning and certain other consequences of external causes
XX	V01–Y98	External causes of morbidity and mortality
XXI	Z00–Z99	Factors influencing health status and contact with health services
XXII	U00–U99	Codes for special purposes

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 (2019), can be browsed freely on the website of the World Health Organisation (WHO). The ICD-10 can also be downloaded in PDF-form.

Endocrine diseases (E00–E35)

Thyroid gland / Thyroid hormone (E00–E07)

• E00 Congenital iodine-deficiency syndrome
• 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
    • Graves' disease
  • 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
    • De Quervain's thyroiditis
  • E06.2 Chronic thyroiditis with transient thyrotoxicosis
  • E06.3 Autoimmune thyroiditis
    • Hashimoto's thyroiditis
  • E06.4 Drug-induced thyroiditis
  • E06.5 Other chronic thyroiditis
    • Riedel's thyroiditis
  • E06.9 Thyroiditis, unspecified
• E07 Other disorders of thyroid
  • E07.0 Hypersecretion of calcitonin
  • E07.1 Dyshormogenetic goitre
  • E07.8 Other specified disorders of thyroid
    • Sick-euthyroid syndrome
  • E07.9 Disorder of thyroid, unspecified

Pancreas / Insulin, glucagon (E10–E16)

Diabetes mellitus (E10–E14)

• E10 Insulin-dependent diabetes mellitus
  • E10.0 Diabetic coma
  • E10.1 Diabetic ketoacidosis
  • E10.2 Diabetic nephropathy
  • E10.3 Diabetic retinopathy
  • E10.4 Diabetic neuropathy
  • E10.5 Diabetic angiopathy
  • E10.6 Diabetic arthropathy
• E11 Non-insulin-dependent diabetes mellitus
  • E11.0 Diabetic coma
  • E11.1 Diabetic ketoacidosis
  • E11.2 Diabetic nephropathy
  • E11.3 Diabetic retinopathy
  • E11.4 Diabetic neuropathy
  • E11.5 Diabetic angiopathy
  • E11.6 Diabetic arthropathy
• E12 Malnutrition-related diabetes mellitus
  • E12.0 Diabetic coma
  • E12.1 Diabetic ketoacidosis
  • E12.2 Diabetic nephropathy
  • E12.3 Diabetic retinopathy
  • E12.4 Diabetic neuropathy
  • E12.5 Diabetic angiopathy
  • E12.6 Diabetic arthropathy
• E13 Other specified diabetes mellitus
  • E13.0 Diabetic coma
  • E13.1 Diabetic ketoacidosis
  • E13.2 Diabetic nephropathy
  • E13.3 Diabetic retinopathy
  • E13.4 Diabetic neuropathy
  • E13.5 Diabetic angiopathy
  • E13.6 Diabetic arthropathy
• E14 Unspecified diabetes mellitus
  • E14.0 Diabetic coma
  • E14.1 Diabetic ketoacidosis
  • E14.2 Diabetic nephropathy
  • E14.3 Diabetic retinopathy
  • E14.4 Diabetic neuropathy
  • E14.5 Diabetic angiopathy
  • E14.6 Diabetic arthropathy

Other disorders of glucose regulation and pancreatic internal secretion (E15–E16)

• E15 Nondiabetic hypoglycaemic coma
  • • Drug-induced insulin coma in nondiabetic
    • Hyperinsulinism with hypoglycaemic coma
    • Hypoglycaemic coma 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

Parathyroid gland / PTH (E20–E21)

• E20 Hypoparathyroidism
  • E20.0 Idiopathic hypoparathyroidism
  • E20.1 Pseudohypoparathyroidism
• E21 Hyperparathyroidism and other disorders of parathyroid gland
  • E21.0 Primary hyperparathyroidism
  • E21.1 Secondary hyperparathyroidism, not elsewhere classified

Pituitary gland / ADH, oxytocin, GH, ACTH, TSH, LH, FSH, prolactin (E22–E23)

• E22 Hyperfunction of pituitary gland
  • E22.0 Acromegaly and pituitary gigantism
  • E22.1 Hyperprolactinaemia
  • E22.2 Syndrome of inappropriate secretion of antidiuretic hormone
    • Central precocious puberty
• 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
  • E23.1 Drug-induced hypopituitarism
  • E23.2 Diabetes insipidus
  • E23.3 Hypothalamic dysfunction, not elsewhere classified
  • E23.6 Other disorders of pituitary gland
    • Abscess of pituitary
    • Adiposogenital dystrophy
  • E23.7 Disorder of pituitary gland, unspecified

Adrenal gland / Aldosterone, cortisol, epinephrine, norepinephrine (E24–E27)

• 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
    • Congenital adrenal hyperplasia
      • Congenital adrenal hyperplasia due to 21-hydroxylase 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
    • Bartter's syndrome
  • E26.9 Hyperaldosteronism, unspecified
• E27 Other disorders of adrenal gland
  • E27.0 Other adrenocortical overactivity
  • E27.1 Primary adrenocortical insufficiency
    • Addison's disease
  • E27.2 Addisonian crisis
  • E27.3 Drug-induced adrenocortical insufficiency
  • E27.4 Other and unspecified adrenocortical insufficiency
    • Hypoaldosteronism
    • Adrenocortical insufficiency NOS
  • E27.5 Adrenomedullary hyperfunction

Gonads / Estrogen, androgens, testosterone, etc. (E28–E30)

• E28 Ovarian dysfunction
  • E28.0 Estrogen excess
  • E28.1 Androgen excess
  • E28.2 Polycystic ovarian syndrome
  • E28.3 Primary ovarian failure
    • Premature menopause NOS
• 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

Other (E31–E35)

• E31 Polyglandular dysfunction
  • E31.0 Autoimmune polyglandular failure
    • Schmidt's syndrome
  • E31.1 Polyglandular hyperfunction
• E32 Diseases of thymus
  • E32.0 Persistent hyperplasia of thymus
    • Hypertrophy of thymus
  • E32.1 Abscess of thymus
• 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
    • Constitutional gigantism
  • E34.5 Androgen resistance syndrome
    • Reifenstein's syndrome
  • E34.8 Other specified endocrine disorders
    • Progeria
• 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

Nutritional diseases (E40–E68)

Malnutrition (E40–E46)

• 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

Other nutritional deficiencies (E50–E64)

• 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
  • E51.1 Beriberi
  • E51.2 Wernicke's encephalopathy
• E52 Niacin deficiency (pellagra)
• E53 Deficiency of other B group vitamins
  • E53.0 Riboflavin deficiency
    • Ariboflavinosis
  • E53.1 Pyridoxine deficiency
  • E53.8 Deficiency of other specified B group vitamins
• E54 Ascorbic acid deficiency
  • Scurvy
• E55 Vitamin D deficiency
  • E55.0 Rickets, active
• E56 Other vitamin deficiencies
  • E56.0 Deficiency of vitamin E
  • E56.1 Deficiency of vitamin K
• 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

Obesity and other hyperalimentation (E65–E68)

• E65 Localized adiposity
  • Fat pad
• E66 Obesity
  • E66.0 Obesity due to excess calories
  • E66.1 Drug-induced obesity
  • E66.2 Extreme obesity with alveolar hypoventilation
    • Pickwickian syndrome
  • E66.8 Other obesity
    • Morbid obesity
  • E66.9 Obesity, unspecified
• E67 Other hyperalimentation
  • E67.0 Hypervitaminosis A
  • E67.1 Hypercarotenaemia
  • E67.2 Megavitamin-B 6 syndrome
  • E67.3 Hypervitaminosis D
• E68 Sequelae of hyperalimentation

Metabolic diseases (E70–E90)

Metabolic disorders of proteins, fats, and carbohydrates (E70–E78)

Amino-acids (E70–E72)

• 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
    • Oculocutaneous albinism (ILDS E70.310)
    • Partial albinism (ILDS E70.312)
    • Oculocutaneous albinism type 1 (tyrosinase-negative) (ILDS E70.314)
    • Oculocutaneous albinism type 2 (tyrosinase positive) (ILDS E70.314)
    • Albinoidism (ILDS E70.318)
    • Waardenburg syndrome (ILDS E70.320)
    • Chédiak–Higashi syndrome (ILDS E70.340)
    • Piebaldism (ILDS E70.350)
    • Tietz syndrome (ILDS E70.358)
    • Hermansky–Pudlak syndrome (ILDS E70.360)
    • Cross syndrome (ILDS E70.380)
  • 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
    • Propionic acidemia
    • Methylmalonic acidemia
    • Isovaleric acidemia
  • 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
    • Cystinuria
    • Cystinosis
    • Hartnup disease
    • Lowe's syndrome
  • 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
    • Lysinuric protein intolerance
  • 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

Carbohydrates (E73–E74)

• E73 Lactose intolerance
• E74 Other disorders of carbohydrate metabolism
  • E74.0 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)
  • E74.1 Disorders of fructose metabolism
    • Essential fructosuria
    • Fructose-1,6-diphosphatase deficiency
    • Hereditary fructose intolerance
  • E74.2 Disorders of galactose metabolism
    • Galactosaemia
    • Galactokinase deficiency
  • E74.3 Other disorders of intestinal carbohydrate absorption
    • Glucose-galactose malabsorption
    • Sucrase deficiency
  • E74.4 Disorders of pyruvate metabolism and gluconeogenesis
    • Deficiency of phosphoenolpyruvate carboxykinase
    • Deficiency of pyruvate carboxylase
    • Deficiency of pyruvate dehydrogenase
  • E74.8 Other specified disorders of carbohydrate metabolism
    • Essential pentosuria
    • Oxalosis
    • Oxaluria
    • Renal glycosuria
  • E74.9 Disorder of carbohydrate metabolism, unspecified

Lipids (E75)

• E75 Disorders of sphingolipid metabolism and other lipid storage disorders
  • E75.0 GM 2 gangliosidosis
    • Sandhoff disease
    • Tay–Sachs disease
  • E75.1 Other gangliosidosis
    • GM 1
    • GM 3
    • Mucolipidosis type IV
  • E75.2 Other sphingolipidosis
    • Gaucher's disease (ILDS E75.220)
    • Niemann–Pick disease (ILDS E75.230)
    • Farber disease (ILDS E75.240)
    • Fabry disease (ILDS E75.250)
  • E75.3 Sphingolipidosis, unspecified
  • E75.4 Neuronal ceroid lipofuscinosis
    • Batten disease (Type 3)
    • Jansky–Bielschowsky 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

Combinations (E76–E78)

• E76 Disorders of glycosaminoglycan metabolism
  • E76.0 Mucopolysaccharidosis, type I
    • Hurler syndrome
  • E76.1 Mucopolysaccharidosis, type II
    • Hunter syndrome
  • E76.2 Other mucopolysaccharidoses
    • Sanfilippo syndrome
    • Morquio syndrome
• E77 Disorders of glycoprotein metabolism
  • E77.0 Defects in post-translational modification of lysosomal enzymes
    • Mucolipidosis II (I-cell disease)
    • Mucolipidosis III (pseudo-Hurler polydystrophy)
  • E77.1 Defects in glycoprotein degradation
    • Aspartylglucosaminuria
    • Fucosidosis
    • Mannosidosis
    • Sialidosis (mucolipidosis I)
  • E77.8 Other disorders of glycoprotein metabolism
  • E77.9 Disorder of glycoprotein metabolism, unspecified
• 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
    • Familial combined hyperlipidaemia
  • E78.5 Hyperlipidaemia, unspecified
  • E78.6 Lipoprotein deficiency
    • Abetalipoproteinaemia
    • High-density lipoprotein deficiency
    • Hypoalphalipoproteinaemia
    • Hypobetalipoproteinaemia (familial)
    • Lecithin cholesterol acyltransferase deficiency
    • Tangier disease

Other metabolic disorders (E79–E90)

• 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 disease (ILDS (ILDS E80.020)
    • Erythropoietic porphyria (ILDS (ILDS E80.030)
    • Erythropoietic coproporphyria (ILDS E80.040)
  • E80.1 Porphyria cutanea tarda
    • Sporadic porphyria cutanea tarda (ILDS E80.110)
    • Familial porphyria cutanea tarda (ILDS E80.120)
  • 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
    • Dubin–Johnson syndrome
    • Rotor syndrome
  • E80.7 Disorder of bilirubin metabolism, unspecified
• E83 Disorders of mineral metabolism
  • E83.0 Disorders of copper metabolism
    • Wilson's disease
    • Menkes disease
  • E83.1 Disorders of iron metabolism
    • Aceruloplasminemia
    • Hemochromatosis
  • E83.2 Disorders of zinc metabolism
    • Acrodermatitis enteropathica
  • 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
    • Hypermagnesemia
    • Hypomagnesemia
  • E83.5 Disorders of calcium metabolism
    • Familial hypocalciuric hypercalcaemia
    • Idiopathic hypercalciuria
• E84 Cystic fibrosis
• E85 Amyloidosis
  • E85.0 Non-neuropathic heredofamilial amyloidosis
    • Familial Mediterranean fever
    • Hereditary amyloid nephropathy
  • E85.1 Neuropathic heredofamilial amyloidosis
    • Amyloid polyneuropathy (Portuguese)
  • E85.2 Heredofamilial amyloidosis, unspecified
  • E85.3 Secondary systemic amyloidosis
    • Haemodialysis-associated amyloidosis
  • E85.4 Organ-limited amyloidosis
    • Localized amyloidosis
  • E85.8 Other amyloidosis
  • E85.9 Amyloidosis, unspecified
• E86 Volume depletion
  • Dehydration
  • Hypovolaemia
• E87 Other disorders of fluid, electrolyte and acid–base balance
  • E87.0 Hyperosmolality and hypernatraemia
  • E87.1 Hypo-osmolality and hyponatraemia
  • E87.2 Acidosis
    • Respiratory acidosis
    • Metabolic acidosis
    • Lactic 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
    • Electrolyte imbalance NOS
    • Hyperchloraemia
    • Hypochloraemia
• E88 Other metabolic disorders
  • E88.0 Disorders of plasma-protein metabolism, not elsewhere classified
    • Alpha-1-antitrypsin deficiency
    • Bisalbuminaemia
  • E88.1 Lipodystrophy, not elsewhere classified
  • E88.2 Lipomatosis, not elsewhere classified
  • E88.8 Other specified metabolic disorders
    • Launois–Bensaude adenolipomatosis
    • Trimethylaminuria
  • E88.9 Metabolic disorder, unspecified
• 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

Excludes

• Autoimmune disease (systemic) NOS (M35.9)
• Certain conditions originating in the perinatal period (P00-P96)
• Complications of pregnancy, childbirth and the puerperium (O00-O9A)
• Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
• Human immunodeficiency virus [HIV] disease (B20)
• Injury, poisoning and certain other consequences of external causes (S00-T88)
• Neoplasms (C00-D49)
• Symptoms, signs, and abnormal clinical and laboratory findings, NEC (R00-R94)

See also

• List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders

1. REDIRECT Template:Metal deficiency and toxicity disorders

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• ICD-10 Chapter II: Neoplasms
• ICD-10 Chapter XVIII: Symptoms, signs and abnormal clinical and laboratory findings
• ICD-10 Chapter XXI: Factors influencing health status and contact with health services
• ICD-10 Chapter I: Certain infectious and parasitic diseases
• ICD-10 Chapter XX: External causes of morbidity and mortality
• ICD-10 Chapter XV: Pregnancy, childbirth and the puerperium
• ICD-10 Chapter VII: Diseases of the eye, adnexa

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