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

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E00-E35 - Endocrine diseases[]

(E00-E07) Thyroid gland / Thyroid hormone[]

(E 00) Congenital iodine-deficiency syndrome

(E01) Iodine-deficiency-related thyroid disorders and allied conditions
- (E 010) Iodine-deficiency-related diffuse (endemic) goitre
- (E 011) Iodine-deficiency-related multinodular (endemic) goitre
- (E 012) Iodine-deficiency-related (endemic) goitre, unspecified
- (E 018) Other iodine-deficiency-related thyroid disorders and allied condition

(E 02) Subclinical iodine-deficiency hypothyroidism
(E03) Other hypothyroidism
- (E 030) Congenital hypothyroidism with diffuse goitre
- (E 031) Congenital hypothyroidism without goitre
- (E 032) Hypothyroidism due to medicaments and other exogenous substances
- (E 033) Postinfectious hypothyroidism
- (E 034) Atrophy of thyroid (acquired)
- (E 035) Myxoedema coma
(E 04) Other nontoxic goitre

(E05) Thyrotoxicosis (hyperthyroidism)
- (E050) Thyrotoxicosis with diffuse goitre
  - Graves' disease
- (E 051) Thyrotoxicosis with toxic single thyroid nodule
- (E 052) Thyrotoxicosis with toxic multinodular goitre
- (E 053) Thyrotoxicosis from ectopic thyroid tissue
- (E 054) Thyrotoxicosis factitia
- (E 055) Thyroid crisis or storm
- (E 058) Other thyrotoxicosis
- (E 059) Thyrotoxicosis, unspecified

(E06) Thyroiditis
- (E 060) Acute thyroiditis
- (E061) Subacute thyroiditis
  - De Quervain's thyroiditis
- (E 062) Chronic thyroiditis with transient thyrotoxicosis
- (E063) Autoimmune thyroiditis
  - Hashimoto's thyroiditis
- (E 064) Drug-induced thyroiditis
- (E 065) Other chronic thyroiditis
- (E 069) Thyroiditis, unspecified

(E07) Other disorders of thyroid
- (E 070) Hypersecretion of calcitonin
- (E 071) Dyshormogenetic goitre
- (E078) Other specified disorders of thyroid
  - Sick-euthyroid syndrome
- (E 079) Disorder of thyroid, 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
(E 10) Insulin-dependent diabetes mellitus
(E 11) Non-insulin-dependent diabetes mellitus
(E 12) Malnutrition-related diabetes mellitus
(E 13) Other specified diabetes mellitus
(E 14) Unspecified diabetes mellitus

(E15-E16) Other disorders of glucose regulation and pancreatic internal secretion[]

(E 15) Nondiabetic hypoglycaemic coma
(E16) Other disorders of pancreatic internal secretion
- (E 160) Drug-induced hypoglycaemia without coma
- (E 161) Other hypoglycaemia
- (E 162) Hypoglycaemia, unspecified
- (E 163) Increased secretion of glucagon
- (E164) Abnormal secretion of gastrin
  - Hypergastrinaemia
  - Zollinger-Ellison syndrome
- (E 168) Other specified disorders of pancreatic internal secretion
- (E 169) Disorder of pancreatic internal secretion, unspecified

(E20-E21) Parathyroid gland / PTH[]

(E20) Hypoparathyroidism
- (E 200) Idiopathic hypoparathyroidism
- (E 201) Pseudohypoparathyroidism

(E21) Hyperparathyroidism and other disorders of parathyroid gland
- (E 210) Primary hyperparathyroidism
- (E 211) Secondary hyperparathyroidism, not elsewhere classified

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

(E22) Hyperfunction of pituitary gland
- (E 220) Acromegaly and pituitary gigantism
- (E 221) Hyperprolactinaemia
- (E222) Syndrome of inappropriate secretion of antidiuretic hormone
  - Central precocious puberty

(E23) Hypofunction and other disorders of pituitary gland
- (E230) 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

- (E 231) Drug-induced hypopituitarism
- (E 232) Diabetes insipidus
- (E 233) Hypothalamic dysfunction, not elsewhere classified

(E24-E27) Adrenal gland / Aldosterone, cortisol, epinephrine, norepinephrine[]

(E24) Cushing's syndrome
- (E 240) Pituitary-dependent Cushing's disease
- (E 241) Nelson's syndrome
- (E 242) Ectopic ACTH syndrome
- (E 243) Alcohol-induced pseudo-Cushing's syndrome
- (E 244) Other Cushing's syndrome
- (E 245) Cushing's syndrome, unspecified

(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
  - Primary aldosteronism due to adrenal hyperplasia (bilateral)
- (E 261) Secondary hyperaldosteronism
- (E268) Other hyperaldosteronism
  - Bartter's syndrome
- (E 269) Hyperaldosteronism, unspecified

(E27) Other disorders of adrenal gland
- (E 270) Other adrenocortical overactivity
- (E271) Primary adrenocortical insufficiency
  - Addison's disease
- (E 272) Addisonian crisis
- (E 273) Drug-induced adrenocortical insufficiency
- (E274) Other and unspecified adrenocortical insufficiency
  - Hypoaldosteronism
  - Adrenocortical insufficiency NOS
- (E 275) Adrenomedullary hyperfunction

(E28-E30) Gonads / Estrogen, androgens, testosterone, etc.[]

(E28) Ovarian dysfunction
- (E 280) Estrogen excess
- (E 281) Androgen excess
- (E 282) Polycystic ovarian syndrome
- (E283) Primary ovarian failure
  - Premature menopause NOS

(E29) Testicular dysfunction
- (E 290) Testicular hyperfunction
- (E291) Testicular hypofunction
  - 5-Alpha-reductase deficiency (with male pseudohermaphroditism)
  - Testicular hypogonadism NOS

(E30) Disorders of puberty, not elsewhere classified
- (E 300) Delayed puberty
- (E 301) Precocious puberty
- (E308) Other disorders of puberty
  - Premature thelarche

(E31-E35) Other[]

(E31) Polyglandular dysfunction
- (E310) Autoimmune polyglandular failure
  - Schmidt's syndrome
- (E 311) Polyglandular hyperfunction

(E32) Diseases of thymus
- (E 320) Persistent hyperplasia of thymus
- (E 321) Abscess of thymus

(E34) Other endocrine disorders
- (E 340) Carcinoid syndrome
- (E 341) Other hypersecretion of intestinal hormones
- (E 342) Ectopic hormone secretion, not elsewhere classified
- (E343) Short stature, not elsewhere classified
  - NOS
  - constitutional
  - Laron-type
  - psychosocial
- (E 344) 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
- (E 350) Disorders of thyroid gland in diseases classified elsewhere
- (E 351) Disorders of adrenal glands in diseases classified elsewhere
- (E 358) Disorders of other endocrine glands in diseases classified elsewhere

E40-68 - Nutritional diseases[]

(E40-E46) Malnutrition[]

(E 40) Kwashiorkor
(E 41) Nutritional marasmus
(E 42) Marasmic kwashiorkor
(E 43) Unspecified severe protein-energy malnutrition
(E 44) Protein-energy malnutrition of moderate and mild degree
(E 45) Retarded development following protein-energy malnutrition
(E 46) Unspecified protein-energy malnutrition

(E50-E64) Other nutritional deficiencies[]

(E50) Vitamin A deficiency
- (E 500) Vitamin A deficiency with conjunctival xerosis
- (E 501) Vitamin A deficiency with Bitot's spot and conjunctival xerosis
- (E 502) Vitamin A deficiency with corneal xerosis
- (E 503) Vitamin A deficiency with corneal ulceration and xerosis
- (E 504) Vitamin A deficiency with keratomalacia
- (E 505) Vitamin A deficiency with night blindness
- (E 506) Vitamin A deficiency with xerophthalmic scars of cornea
- (E507) Other ocular manifestations of vitamin A deficiency
  - Xerophthalmia NOS
(E51) Thiamine deficiency
- (E 511) Beriberi
- (E 512) Wernicke's encephalopathy
(E 52) Niacin deficiency (pellagra)
(E53) Deficiency of other B group vitamins
- (E530) Riboflavin deficiency
  - Ariboflavinosis
- (E 531) Pyridoxine deficiency
- (E 538) Deficiency of other specified B group vitamins
(E54) Ascorbic acid deficiency
- Scurvy
(E55) Vitamin D deficiency
- (E 550) Rickets, active
(E56) Other vitamin deficiencies
- (E 560) Deficiency of vitamin E
- (E 561) Deficiency of vitamin K
(E 58) Dietary calcium deficiency
(E 59) Dietary selenium deficiency
(E 60) Dietary zinc deficiency
(E61) Deficiency of other nutrient elements
- (E 611) Iron deficiency
- (E 612) Magnesium deficiency
- (E 613) Manganese deficiency
- (E 614) Chromium deficiency
- (E 615) Molybdenum deficiency
- (E 616) Vanadium deficiency
(E63) Other nutritional deficiencies
- (E 630) Essential fatty acid (EFA) deficiency
(E 64) Sequelae of malnutrition and other nutritional deficiencies

(E65-E68) Obesity and other hyperalimentation[]

(E 65) Localized adiposity
(E 66) Obesity
(E67) Other hyperalimentation
- (E 670) Hypervitaminosis A
- (E 673) Hypervitaminosis D
(E 68) 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
- (E 700) Classical phenylketonuria
- (E 701) Other hyperphenylalaninaemias
- (E702) Disorders of tyrosine metabolism
  - Alkaptonuria (ILDS E70.210)
  - Ochronosis (ILDS E70.230)
  - Tyrosinaemia
- (E703) Albinism
  - Chediak-Higashi syndrome
  - Cross syndrome
  - Hermansky-Pudlak syndrome

(E71) Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
- (E 710) Maple-syrup-urine disease
- (E711) Other disorders of branched-chain amino-acid metabolism
  - Propionic acidemia
  - Methylmalonic acidemia
  - Isovaleric acidemia
- (E 712) 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
  - Lowe's syndrome
- (E721) Disorders of sulfur-bearing amino-acid metabolism
  - Cystathioninuria
  - Homocystinuria
  - Methioninaemia
  - Sulfite oxidase deficiency
- (E722) Disorders of urea cycle metabolism
  - Argininaemia
  - Argininosuccinic aciduria
  - Citrullinaemia
  - Hyperammonaemia
- (E723) Disorders of lysine and hydroxylysine metabolism
  - Glutaric aciduria
  - Hydroxylysinaemia
  - Hyperlysinaemia
- (E724) Disorders of ornithine metabolism
  - Ornithinaemia (types I, II)
- (E725) Disorders of glycine metabolism
  - Hyperhydroxyprolinaemia
  - Hyperprolinaemia (types I, II)
  - Non-ketotic hyperglycinaemia
  - Sarcosinaemia

(E73-E74) Carbohydrates[]

(E 73) 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) Lipids[]

(E75) Disorders of sphingolipid metabolism and other lipid storage disorders
- (E750) GM 2 gangliosidosis
  - Sandhoff disease
  - Tay-Sachs disease
- (E751) Other gangliosidosis
  - GM 1
  - GM 3
  - Mucolipidosis IV
- (E752) 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)
- (E 753) Sphingolipidosis, unspecified
- (E754) Neuronal ceroid lipofuscinosis
  - Batten disease (Type 3)
  - Bielschowsky-Jansky disease (Type 2)
  - Kufs disease (Type 4)
  - Spielmeyer-Vogt disease (Type 3)
- (E755) Other lipid storage disorders
  - Cerebrotendineous xanthomatosis
  - Wolman's disease
- (E 756) Lipid storage disorder, unspecified

(E76-E78) Combinations[]

(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
  - Mucolipidosis II (I-cell disease)
  - Mucolipidosis III (pseudo-Hurler polydystrophy)
- (E771) Defects in glycoprotein degradation
  - Aspartylglucosaminuria
  - Fucosidosis
  - Mannosidosis
  - Sialidosis (mucolipidosis I)

(E78) Disorders of lipoprotein metabolism and other lipidaemias
- (E780) Pure 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
- (E 785) Hyperlipidaemia, unspecified
- (E786) Lipoprotein deficiency
  - Abetalipoproteinaemia
  - High-density lipoprotein deficiency
  - Hypoalphalipoproteinaemia
  - Hypobetalipoproteinaemia (familial)
  - Lecithin cholesterol acyltransferase deficiency
  - Tangier disease

(E79-E90) Other metabolic disorders[]

(E79) Disorders of purine and pyrimidine metabolism
- (E 790) Hyperuricaemia without signs of inflammatory arthritis and tophaceous disease
- (E 791) Lesch-Nyhan syndrome
- (E798) Other disorders of purine and pyrimidine metabolism
  - Hereditary xanthinuria

(E80) Disorders of porphyrin and bilirubin metabolism
- (E800) 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)
- (E801) Porphyria cutanea tarda
  - Sporadic porphyria cutanea tarda (ILDS E80.110)
  - Familial porphyria cutanea tarda (ILDS E80.120)
- (E802) 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)
- (E803) Defects of catalase and peroxidase
  - Acatalasia (Takahara)
- (E 804) Gilbert's syndrome
- (E 805) Crigler-Najjar syndrome
- (E806) Other disorders of bilirubin metabolism
  - Dubin-Johnson syndrome
  - Rotor's syndrome
- (E 807) Disorder of bilirubin metabolism, unspecified

(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
  - Acrodermatitis enteropathica
- (E833) Disorders of phosphorus metabolism
  - Acid phosphatase deficiency
  - Familial hypophosphataemia
  - Hypophosphatasia
  - Vitamin-D-resistant osteomalacia
  - Vitamin-D-resistant rickets
- (E834) Disorders of magnesium metabolism
  - Hypermagnesemia
  - Hypomagnesemia
- (E835) Disorders of calcium metabolism
  - Familial hypocalciuric hypercalcaemia
  - Idiopathic hypercalciuria

(E 84) 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
- (E 870) Hyperosmolality and hypernatraemia
- (E 871) Hypo-osmolality and hyponatraemia
- (E872) Acidosis
  - Respiratory acidosis
  - Metabolic acidosis
  - Lactic acidosis
- (E 873) Alkalosis
- (E 874) Mixed disorder of acid-base balance
- (E 875) Hyperkalaemia
- (E 876) Hypokalaemia
- (E 877) 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
- (E 881) Lipodystrophy, not elsewhere classified
- (E 882) Lipomatosis, not elsewhere classified

(E89) Postprocedural endocrine and metabolic disorders, not elsewhere classified
- (E 890) Postprocedural hypothyroidism
- (E 891) Postprocedural hypoinsulinaemia
- (E 892) Postprocedural hypoparathyroidism
- (E 893) Postprocedural hypopituitarism
- (E 894) Postprocedural ovarian failure
- (E 895) Postprocedural testicular hypofunction
- (E 896) Postprocedural adrenocortical(-medullary) hypofunction

(E 90) Nutritional and metabolic disorders in diseases classified elsewhere

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

Contents

E00-E35 - Endocrine diseases[]

(E00-E07) Thyroid gland / Thyroid hormone[]

(E10-E16) Pancreas / Insulin, glucagon[]

(E10-E14) Diabetes mellitus[]

(E15-E16) Other disorders of glucose regulation and pancreatic internal secretion[]

(E20-E21) Parathyroid gland / PTH[]

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

(E24-E27) Adrenal gland / Aldosterone, cortisol, epinephrine, norepinephrine[]

(E28-E30) Gonads / Estrogen, androgens, testosterone, etc.[]

(E31-E35) Other[]

E40-68 - Nutritional diseases[]

(E40-E46) Malnutrition[]

(E50-E64) Other nutritional deficiencies[]

(E65-E68) Obesity and other hyperalimentation[]

E70-E90 - Metabolic diseases[]

(E70-E79) Metabolic disorders of proteins, fats, and carbohydrates[]

(E70-E72) Amino-acids[]

(E73-E74) Carbohydrates[]

(E75) Lipids[]

(E76-E78) Combinations[]

(E79-E90) Other metabolic disorders[]

See also[]

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