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  • ICD-10_Chapter_IV:_Endocrine,_nutritional_and_metabolic_diseases

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



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Contents

E00-E35 - Endocrine diseases

(E00-E07) Thyroid gland / Thyroid hormone

  • (E00.) Congenital iodine-deficiency syndrome
  • (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

(E10-E16) Pancreas / Insulin, glucagon

(E10-E14) 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 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

(E20-E21) Parathyroid gland / PTH

  • (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

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

  • (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

(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
      • 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

(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
      • 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

(E31-E35) Other

  • (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
    • (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
    • (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

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

(E65-E68) Obesity and other hyperalimentation

  • (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

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

  • (E84.) Cystic fibrosis
  • (E85.) Amyloidosis
    • (E85.0) Non-neuropathic heredofamilial amyloidosis
    • (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
  • (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

See also

v • d • e
Endocrine pathology: endocrine diseases (E00-35, 240-259)
ThyroidHypothyroidism (Iodine deficiency, Cretinism, Congenital hypothyroidism, Goitre, Myxedema) - Hyperthyroidism (Graves disease, Toxic multinodular goitre, Teratoma with thyroid tissue or Struma ovarii) - Thyroiditis (De Quervain's thyroiditis, Hashimoto's thyroiditis, Riedel's thyroiditis) - Euthyroid sick syndrome
PancreasDiabetes mellitus (type 1, type 2, coma, angiopathy, ketoacidosis, nephropathy, neuropathy, retinopathy) - Hypoglycemia - Hyperinsulinism - Zollinger-Ellison syndrome
ParathyroidHypoparathyroidism (Pseudohypoparathyroidism) - Hyperparathyroidism (Primary, Secondary, Tertiary)
PituitaryHyperpituitarism (Acromegaly, Hyperprolactinaemia, SIADH) - Hypopituitarism (Simmonds' disease/Sheehan's syndrome, Kallmann syndrome, Growth hormone deficiency, Diabetes insipidus) - Adiposogenital dystrophy - Empty sella syndrome
AdrenalCushing's syndrome (Nelson's syndrome, Pseudo-Cushing's syndrome) - CAH (due to 21-hydroxylase deficiency) - Hyperaldosteronism (Conn syndrome, Bartter syndrome) - Adrenal insufficiency (Addison's disease) - Hypoaldosteronism
Gonadsovarian dysfunction (Polycystic ovary syndrome, Premature ovarian failure) - testicular dysfunction (5-alpha-reductase deficiency) - general (Hypogonadism, Delayed puberty, Precocious puberty)
OtherAutoimmune polyendocrine syndrome - Carcinoid syndrome - Short stature (Laron syndrome, Psychogenic dwarfism) - Gigantism - Androgen insensitivity syndrome - Progeria - Multiple endocrine neoplasia (1, 2)
v • d • e
Nutritional pathology (E40-68, 260-269)
MalnutritionKwashiorkor - Marasmus
Other underconsumptionB vitamins: B1: Beriberi/Wernicke's encephalopathy, B2: Ariboflavinosis, B3: Pellagra, B6: Pyridoxine deficiency, B7: Biotin deficiency, B9: Folate deficiency, B12: Vitamin B12 deficiency

other vitamins: A: Vitamin A deficiency/Bitot's spots, C: Scurvy, D: Rickets/Osteomalacia

mineral: Zinc deficiency - Iron deficiency, Magnesium deficiency - Chromium deficiency
HyperalimentationObesity - Hypervitaminosis A - Hypervitaminosis D
v • d • e
Metabolic pathology / Inborn error of metabolism (E70-90, 270-279)
Amino acidAromatic (Phenylketonuria, Alkaptonuria, Ochronosis, Tyrosinemia, Albinism, Histidinemia) - Organic acidemias (Maple syrup urine disease, Propionic acidemia, Methylmalonic acidemia, Isovaleric acidemia, 3-Methylcrotonyl-CoA carboxylase deficiency) - Transport (Cystinuria, Cystinosis, Hartnup disease, Fanconi syndrome, Oculocerebrorenal syndrome) - Sulfur (Homocystinuria, Cystathioninuria) - Urea cycle disorder (N-Acetylglutamate synthase deficiency, Carbamoyl phosphate synthetase I deficiency, Ornithine transcarbamylase deficiency, Citrullinemia, Argininosuccinic aciduria, Hyperammonemia) - Glutaric acidemia type 1 - Hyperprolinemia - Sarcosinemia
CarbohydrateLactose intolerance - Glycogen storage disease (type I, type II, type III, type IV, type V, type VI, type VII) - fructose metabolism (Fructose intolerance, Fructose bisphosphatase deficiency, Essential fructosuria) - galactose metabolism (Galactosemia, Galactose-1-phosphate uridylyltransferase galactosemia, Galactokinase deficiency) - other intestinal carbohydrate absorption (Glucose-galactose malabsorption, Sucrose intolerance) - pyruvate metabolism and gluconeogenesis (PCD, PDHA) - Pentosuria - Renal glycosuria
Lipid storageSphingolipidoses/Gangliosidoses: GM2 gangliosidoses (Sandhoff disease, Tay-Sachs disease) - GM1 gangliosidoses - Mucolipidosis type IV - Gaucher's disease - Niemann-Pick disease - Farber disease - Fabry's disease - Metachromatic leukodystrophy - Krabbe disease
Neuronal ceroid lipofuscinosis (Batten disease) - Cerebrotendineous xanthomatosis - Cholesteryl ester storage disease (Wolman disease)
Fatty acid metabolismLipoprotein/lipidemias: Hyperlipidemia - Hypercholesterolemia - Familial hypercholesterolemia - Xanthoma - Combined hyperlipidemia - Lecithin cholesterol acyltransferase deficiency - Tangier disease - Abetalipoproteinemia
Fatty acid: Adrenoleukodystrophy - Acyl-coA dehydrogenase (Short-chain, Medium-chain, Long-chain 3-hydroxy, Very long-chain) - Carnitine (Primary, I, II)
MineralCu Wilson's disease/Menkes disease - Fe Haemochromatosis - Zn Acrodermatitis enteropathica - PO43�' Hypophosphatemia/Hypophosphatasia - Mg2+ Hypermagnesemia/Hypomagnesemia - Ca2+ Hypercalcaemia/Hypocalcaemia/Disorders of calcium metabolism
Fluid, electrolyte
and acid-base balance		Electrolyte disturbance - Na+ Hypernatremia/Hyponatremia - Acidosis (Metabolic, Respiratory, Lactic) - Alkalosis (Metabolic, Respiratory) - Mixed disorder of acid-base balance - H2O Dehydration/Hypervolemia - K+ Hypokalemia/Hyperkalemia - Cl�' Hyperchloremia/Hypochloremia
Purine and pyrimidineHyperuricemia - Lesch-Nyhan syndrome - Xanthinuria
PorphyrinAcute intermittent, Gunther's, Cutanea tarda, Erythropoietic, Hepatoerythropoietic, Hereditary copro-, Variegate
BilirubinUnconjugated (Lucey-Driscoll syndrome, Gilbert's syndrome, Crigler-Najjar syndrome) - Conjugated (Dubin-Johnson syndrome, Rotor syndrome)
GlycosaminoglycanMucopolysaccharidosis - 1:Hurler/Hunter - 3:Sanfilippo - 4:Morquio - 6:Maroteaux-Lamy - 7:Sly
GlycoproteinMucolipidosis - I-cell disease - Pseudo-Hurler polydystrophy - Aspartylglucosaminuria - Fucosidosis - Alpha-mannosidosis - Sialidosis
OtherAlpha 1-antitrypsin deficiency - Cystic fibrosis - Amyloidosis (Familial Mediterranean fever) - Acatalasia
 
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "ICD-10_Chapter_IV:_Endocrine,_nutritional_and_metabolic_diseases". A list of authors is available in Wikipedia.
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