ICD-10_Chapter_IV:_Endocrine,_nutritional_and_metabolic_diseases

Sex

Go to The Main Page

Add Sex to favorite!

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

The introduction to this article provides insufficient context for those unfamiliar with the subject.
Please help improve the article with a good introductory style.

Contents

1 E00-E35 - Endocrine diseases

1.1 (E00-E07) Thyroid gland / Thyroid hormone

1.2 (E10-E16) Pancreas / Insulin, glucagon

1.2.1 (E10-E14) Diabetes mellitus

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

1.3 (E20-E21) Parathyroid gland / PTH

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

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

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

1.7 (E31-E35) Other

2 E40-68 - Nutritional diseases

2.1 (E40-E46) Malnutrition

2.2 (E50-E64) Other nutritional deficiencies

2.3 (E65-E68) Obesity and other hyperalimentation

3 E70-E90 - Metabolic diseases

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

3.1.1 (E70-E72) Amino-acids

3.1.2 (E73-E74) Carbohydrates

3.1.3 (E75) Lipids

3.1.4 (E76-E78) Combinations

3.2 (E79-E90) Other metabolic disorders

4 See also

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 01.0) Iodine-deficiency-related diffuse (endemic) goitre
- (E 01.1) Iodine-deficiency-related multinodular (endemic) goitre
- (E 01.2) Iodine-deficiency-related (endemic) goitre, unspecified
- (E 01.8) Other iodine-deficiency-related thyroid disorders and allied condition

(E 02.) Subclinical iodine-deficiency hypothyroidism
(E03.) Other hypothyroidism
- (E 03.0) Congenital hypothyroidism with diffuse goitre
- (E 03.1) Congenital hypothyroidism without goitre
- (E 03.2) Hypothyroidism due to medicaments and other exogenous substances
- (E 03.3) Postinfectious hypothyroidism
- (E 03.4) Atrophy of thyroid (acquired)
- (E 03.5) Myxoedema coma
(E 04.) Other nontoxic goitre

(E05.) Thyrotoxicosis (hyperthyroidism)
- (E05.0) Thyrotoxicosis with diffuse goitre
  - Graves' disease
- (E 05.1) Thyrotoxicosis with toxic single thyroid nodule
- (E 05.2) Thyrotoxicosis with toxic multinodular goitre
- (E 05.3) Thyrotoxicosis from ectopic thyroid tissue
- (E 05.4) Thyrotoxicosis factitia
- (E 05.5) Thyroid crisis or storm
- (E 05.8) Other thyrotoxicosis
- (E 05.9) Thyrotoxicosis, unspecified

(E06.) Thyroiditis
- (E 06.0) Acute thyroiditis
- (E06.1) Subacute thyroiditis
  - De Quervain's thyroiditis
- (E 06.2) Chronic thyroiditis with transient thyrotoxicosis
- (E06.3) Autoimmune thyroiditis
  - Hashimoto's thyroiditis
- (E 06.4) Drug-induced thyroiditis
- (E06.5) Other chronic thyroiditis
  - Riedel's thyroiditis
- (E 06.9) Thyroiditis, unspecified

(E07.) Other disorders of thyroid
- (E 07.0) Hypersecretion of calcitonin
- (E 07.1) Dyshormogenetic goitre
- (E07.8) Other specified disorders of thyroid
  - Sick-euthyroid syndrome
- (E 07.9) 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

(E15.) Nondiabetic hypoglycaemic coma

(E16.) Other disorders of pancreatic internal secretion
- (E 16.0) 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
- (E 16.2) Hypoglycaemia, unspecified
- (E 16.3) Increased secretion of glucagon
- (E16.4) Abnormal secretion of gastrin
  - Hypergastrinaemia
  - Zollinger-Ellison syndrome
- (E 16.8) Other specified disorders of pancreatic internal secretion
- (E 16.9) Disorder of pancreatic internal secretion, unspecified

(E20-E21) Parathyroid gland / PTH

(E20.) Hypoparathyroidism
- (E 20.0) Idiopathic hypoparathyroidism
- (E 20.1) Pseudohypoparathyroidism

(E21.) Hyperparathyroidism and other disorders of parathyroid gland
- (E 21.0) Primary hyperparathyroidism
- (E 21.1) Secondary hyperparathyroidism, not elsewhere classified

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

(E22.) Hyperfunction of pituitary gland
- (E 22.0) Acromegaly and pituitary gigantism
- (E 22.1) 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
- (E 23.1) Drug-induced hypopituitarism
- (E 23.2) Diabetes insipidus
- (E 23.3) Hypothalamic dysfunction, not elsewhere classified
- (E23.6) Other disorders of pituitary gland
  - Abscess of pituitary
  - Adiposogenital dystrophy
- (E 23.7) Disorder of pituitary gland, unspecified

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

(E24.) Cushing's syndrome
- (E 24.0) Pituitary-dependent Cushing's disease
- (E 24.1) Nelson's syndrome
- (E 24.2) Ectopic ACTH syndrome
- (E 24.3) Alcohol-induced pseudo-Cushing's syndrome
- (E 24.4) Other Cushing's syndrome
- (E 24.5) 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)
- (E 26.1) Secondary hyperaldosteronism
- (E26.8) Other hyperaldosteronism
  - Bartter's syndrome
- (E 26.9) Hyperaldosteronism, unspecified

(E27.) Other disorders of adrenal gland
- (E 27.0) Other adrenocortical overactivity
- (E27.1) Primary adrenocortical insufficiency
  - Addison's disease
- (E 27.2) Addisonian crisis
- (E 27.3) Drug-induced adrenocortical insufficiency
- (E27.4) Other and unspecified adrenocortical insufficiency
  - Hypoaldosteronism
  - Adrenocortical insufficiency NOS
- (E 27.5) Adrenomedullary hyperfunction

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

(E28.) Ovarian dysfunction
- (E 28.0) Estrogen excess
- (E 28.1) Androgen excess
- (E 28.2) Polycystic ovarian syndrome
- (E28.3) Primary ovarian failure
  - Premature menopause NOS

(E29.) Testicular dysfunction
- (E 29.0) Testicular hyperfunction
- (E29.1) Testicular hypofunction
  - 5-Alpha-reductase deficiency (with male pseudohermaphroditism)
  - Testicular hypogonadism NOS

(E30.) Disorders of puberty, not elsewhere classified
- (E 30.0) Delayed puberty
- (E 30.1) Precocious puberty
- (E30.8) Other disorders of puberty
  - Premature thelarche

(E31-E35) Other

(E31.) Polyglandular dysfunction
- (E31.0) Autoimmune polyglandular failure
  - Schmidt's syndrome
- (E 31.1) Polyglandular hyperfunction

(E32.) Diseases of thymus
- (E32.0) Persistent hyperplasia of thymus
  - Hypertrophy of thymus
- (E 32.1) Abscess of thymus

(E34.) Other endocrine disorders
- (E 34.0) Carcinoid syndrome
- (E 34.1) Other hypersecretion of intestinal hormones
- (E 34.2) 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
- (E 35.0) Disorders of thyroid gland in diseases classified elsewhere
- (E 35.1) Disorders of adrenal glands in diseases classified elsewhere
- (E 35.8) 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 50.0) Vitamin A deficiency with conjunctival xerosis
- (E 50.1) Vitamin A deficiency with Bitot's spot and conjunctival xerosis
- (E 50.2) Vitamin A deficiency with corneal xerosis
- (E 50.3) Vitamin A deficiency with corneal ulceration and xerosis
- (E 50.4) Vitamin A deficiency with keratomalacia
- (E 50.5) Vitamin A deficiency with night blindness
- (E 50.6) Vitamin A deficiency with xerophthalmic scars of cornea
- (E50.7) Other ocular manifestations of vitamin A deficiency
  - Xerophthalmia NOS
(E51.) Thiamine deficiency
- (E 51.1) Beriberi
- (E 51.2) Wernicke's encephalopathy
(E 52.) Niacin deficiency (pellagra)
(E53.) Deficiency of other B group vitamins
- (E53.0) Riboflavin deficiency
  - Ariboflavinosis
- (E 53.1) Pyridoxine deficiency
- (E 53.8) Deficiency of other specified B group vitamins
(E54.) Ascorbic acid deficiency
- Scurvy
(E55.) Vitamin D deficiency
- (E 55.0) Rickets, active
(E56.) Other vitamin deficiencies
- (E 56.0) Deficiency of vitamin E
- (E 56.1) 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 61.1) Iron deficiency
- (E 61.2) Magnesium deficiency
- (E 61.3) Manganese deficiency
- (E 61.4) Chromium deficiency
- (E 61.5) Molybdenum deficiency
- (E 61.6) Vanadium deficiency
(E63.) Other nutritional deficiencies
- (E 63.0) Essential fatty acid (EFA) deficiency
(E 64.) Sequelae of malnutrition and other nutritional deficiencies

(E65-E68) Obesity and other hyperalimentation

(E65.) Localized adiposity
- Fat pad

(E66.) Obesity
- (E 66.0) Obesity due to excess calories
- (E 66.1) Drug-induced obesity
- (E66.2) Extreme obesity with alveolar hypoventilation
  - Pickwickian syndrome
- (E66.8) Other obesity
  - Morbid obesity
- (E 66.9) Obesity, unspecified

(E67.) Other hyperalimentation
- (E 67.0) Hypervitaminosis A
- (E 67.1) Hypercarotenaemia
- (E 67.2) Megavitamin-B 6 syndrome
- (E 67.3) 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 70.0) Classical phenylketonuria
- (E 70.1) 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's syndrome (ILDS E70.320)
  - Chediak-Higashi syndrome (ILDS E70.340)
  - Piebaldism (ILDS E70.350)
  - Tietz's 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
- (E 70.9) Disorder of aromatic amino-acid metabolism, unspecified

(E71.) Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
- (E 71.0) Maple-syrup-urine disease
- (E71.1) Other disorders of branched-chain amino-acid metabolism
- (E 71.2) 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
- (E72.2) Disorders of urea cycle metabolism
- (E72.3) Disorders of lysine and hydroxylysine metabolism
- (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

(E 73.) Lactose intolerance

(E74.) Other disorders of carbohydrate metabolism
- (E74.0) Glycogen storage disease
- (E74.1) Disorders of fructose metabolism
- (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
- (E74.8) Other specified disorders of carbohydrate metabolism
- (E 74.9) Disorder of carbohydrate metabolism, unspecified

(E75) Lipids

(E75.) Disorders of sphingolipid metabolism and other lipid storage disorders
- (E75.0) GM 2 gangliosidosis
  - Sandhoff disease
  - Tay-Sachs disease
- (E75.1) Other gangliosidosis
- (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)
- (E 75.3) 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
- (E 75.6) Lipid storage disorder, unspecified

(E76-E78) Combinations

(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

(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