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E00-E35 - Endocrine diseases[]

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

  • (E00) Congenital iodine-deficiency syndrome
  • (E01) Iodine-deficiency-related thyroid disorders and allied conditions
    • (E010) Iodine-deficiency-related diffuse (endemic) goitre
    • (E011) Iodine-deficiency-related multinodular (endemic) goitre
    • (E012) Iodine-deficiency-related (endemic) goitre, unspecified
    • (E018) Other iodine-deficiency-related thyroid disorders and allied condition
  • (E07) Other disorders of thyroid
    • (E070) Hypersecretion of calcitonin
    • (E071) Dyshormogenetic goitre
    • (E078) Other specified disorders of thyroid
      • Sick-euthyroid syndrome
    • (E079) 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
  • (E16) Other disorders of 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[]

  • (E71) Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
    • (E710) Maple-syrup-urine disease
    • (E711) Other disorders of branched-chain amino-acid metabolism
    • (E712) 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[]

(E75) Lipids[]

(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
  • (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
    • (E785) Hyperlipidaemia, unspecified
    • (E786) Lipoprotein deficiency
      • Abetalipoproteinaemia
      • High-density lipoprotein deficiency
      • Hypoalphalipoproteinaemia
      • Hypobetalipoproteinaemia (familial)
      • Lecithin cholesterol acyltransferase deficiency
      • Tangier disease

(E79-E90) Other metabolic disorders[]

  • (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)
    • (E804) Gilbert's syndrome
    • (E805) Crigler-Najjar syndrome
    • (E806) Other disorders of bilirubin metabolism
      • Dubin-Johnson syndrome
      • Rotor's syndrome
    • (E807) Disorder of bilirubin metabolism, unspecified
  • (E88) Other metabolic disorders
    • (E880) Disorders of plasma-protein metabolism, not elsewhere classified
      • Alpha-1-antitrypsin deficiency
    • (E881) Lipodystrophy, not elsewhere classified
    • (E882) Lipomatosis, not elsewhere classified

See also[]


ru:МКБ-10: Класс IV
th:ICD-10 บท E: โรคต่อใร้ท่อโภชนาการและกระบวนการสร้างและสลาย
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