List of ICD-9 codes 240-279: Endocrine, nutritional and metabolic diseases, and immunity disorders
Additional recommended knowledge
3. Endocrine, nutritional and metabolic diseases, and immunity disorders (240-279)
disorders of thyroid gland (240-246)
- (240) Simple and unspecified goiter
- (241) Nontoxic nodular goiter
- (242) Thyrotoxicosis with or without goiter
- (243) Congenital hypothyroidism
- (244) Acquired hypothyroidism
- (244.0) Hypothyroidism, post-surgical
- (244.1) Hypothyroidism, post-ablative
- (244.9) Hypothyroidism, unspec.
- (245) Thyroiditis
- (245.0) Thyroiditis, acute
- (245.1) Thyroiditis, subacute
- (245.2) Thyroiditis, chronic, Hashimoto's
- (246) Other disorders of thyroid
diseases of other endocrine glands (250-259)
- Note: for 250-259, the following fifth digit can be added:
- (250) Diabetes mellitus
- (251) Other disorders of pancreatic internal secretion
- (252) Disorders of parathyroid gland
- (252.0) Hyperparathyroidism, unspec.
- (252.01) Hyperparathyroidism, primary
- (252.1) Hypoparathyroidism
- (253) Disorders of the pituitary gland and its hypothalamic control
- (254) Diseases of thymus gland
- (255) Disorders of adrenal glands
- (255.0) Cushing's syndrome
- (256) Ovarian dysfunction
- (256.2) Ovarian failure, postablative
- (256.39) Ovarian failure, other
- (256.4) Ovaries, polycystic
- (257) Testicular dysfunction
- (257.2) Testicular hypofunction
- (258) Polyglandular dysfunction and related disorders
- (259) Other endocrine disorders
- (259.0) Puberty, delayed
- (259.1) Sexual precocity
- (260) Kwashiorkor
- (261) Nutritional marasmus
- (262) Other severe protein-calorie malnutrition
- (263) Other and unspecified protein-calorie malnutrition
- (264) Vitamin A deficiency
- (264.0) With conjunctival xerosis
- (264.1) With conjunctival xerosis and Bitot's spot
- (264.2) With corneal xerosis
- (264.3) With corneal ulceration and xerosis
- (264.4) With keratomalacia
- (264.5) With night blindness
- (264.6) With xerophthalmic scars of cornea
- (264.7) Other ocular manifestations of vitamin A deficiency
- (264.8) Other manifestations of vitamin A deficiency
- (264.9) Unspecified vitamin A deficiency
- (265) Thiamine and niacin deficiency states
- (265.0) Beriberi
- (265.1) Other and unspecified manifestations of thiamine deficiency
- Wernicke's encephalopathy
- (265.2) Pellagra
- (266) Deficiency of B-complex components
- (267) Ascorbic acid deficiency
- (268) Vitamin D deficiency
- (269) Other nutritional deficiencies
- (269.0) Deficiency of vitamin K
- (269.1) Deficiency of other vitamins
- (269.2) Unspecified vitamin deficiency
- (269.3) Mineral deficiency, not elsewhere classified
other metabolic and immunity disorders (270-279)
- (273) Disorders of plasma protein metabolism
- (273.0) Polyclonal hypergammaglobulinemia
- (273.1) Monoclonal paraproteinemia
- (273.2) Other paraproteinemias
- (273.3) Macroglobulinemia
- Waldenström macroglobulinemia
- (273.8) Other disorders of plasma protein metabolism
- (274) Gout
- (274.0) Gouty arthropathy
- (275) Disorders of mineral metabolism
- (276) Disorders of fluid, electrolyte, and acid-base balance
- (277) Other and unspecified disorders of metabolism
- (278) Obesity and other hyperalimentation
- (278.0) Obesity, NOS
- (278.1) Localized adiposity
- (278.2) Hypervitaminosis A
- (278.3) Hypercarotinemia
- (278.4) Hypervitaminosis D
- (279) Disorders involving the immune mechanism
- (279.0) Deficiency of humoral immunity
- (279.1) Deficiency of cell-mediated immunity
- (279.11) DiGeorge syndrome
- (279.12) Wiskott-Aldrich syndrome
- (279.2) Combined immunity deficiency
- Severe combined immunodeficiency
See also
| Endocrine pathology: endocrine diseases (E00-35, 240-259) |
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| Thyroid | Hypothyroidism (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 |
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| Pancreas | Diabetes mellitus (type 1, type 2, coma, angiopathy, ketoacidosis, nephropathy, neuropathy, retinopathy) - Hypoglycemia - Hyperinsulinism - Zollinger-Ellison syndrome |
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| Parathyroid | Hypoparathyroidism (Pseudohypoparathyroidism) - Hyperparathyroidism (Primary, Secondary, Tertiary) |
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| Pituitary | Hyperpituitarism (Acromegaly, Hyperprolactinaemia, SIADH) - Hypopituitarism (Simmonds' disease/Sheehan's syndrome, Kallmann syndrome, Growth hormone deficiency, Diabetes insipidus) - Adiposogenital dystrophy - Empty sella syndrome |
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| Adrenal | Cushing'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 |
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| Gonads | ovarian dysfunction (Polycystic ovary syndrome, Premature ovarian failure) - testicular dysfunction (5-alpha-reductase deficiency) - general (Hypogonadism, Delayed puberty, Precocious puberty) |
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| Other | Autoimmune polyendocrine syndrome - Carcinoid syndrome - Short stature (Laron syndrome, Psychogenic dwarfism) - Gigantism - Androgen insensitivity syndrome - Progeria - Multiple endocrine neoplasia (1, 2) |
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| Nutritional pathology (E40-68, 260-269) |
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| Malnutrition | Kwashiorkor - Marasmus |
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| Other underconsumption | B 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 |
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| Hyperalimentation | Obesity - Hypervitaminosis A - Hypervitaminosis D |
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| Metabolic pathology / Inborn error of metabolism (E70-90, 270-279) |
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| Amino acid | Aromatic (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 |
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| Carbohydrate | Lactose 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 |
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| Lipid storage | Sphingolipidoses/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) |
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| Fatty acid metabolism | Lipoprotein/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) |
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| Mineral | Cu Wilson's disease/Menkes disease - Fe Haemochromatosis - Zn Acrodermatitis enteropathica - PO43�' Hypophosphatemia/Hypophosphatasia - Mg2+ Hypermagnesemia/Hypomagnesemia - Ca2+ Hypercalcaemia/Hypocalcaemia/Disorders of calcium metabolism |
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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 |
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| Purine and pyrimidine | Hyperuricemia - Lesch-Nyhan syndrome - Xanthinuria |
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| Porphyrin | Acute intermittent, Gunther's, Cutanea tarda, Erythropoietic, Hepatoerythropoietic, Hereditary copro-, Variegate |
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| Bilirubin | Unconjugated (Lucey-Driscoll syndrome, Gilbert's syndrome, Crigler-Najjar syndrome) - Conjugated (Dubin-Johnson syndrome, Rotor syndrome) |
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| Glycosaminoglycan | Mucopolysaccharidosis - 1:Hurler/Hunter - 3:Sanfilippo - 4:Morquio - 6:Maroteaux-Lamy - 7:Sly |
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| Glycoprotein | Mucolipidosis - I-cell disease - Pseudo-Hurler polydystrophy - Aspartylglucosaminuria - Fucosidosis - Alpha-mannosidosis - Sialidosis |
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| Other | Alpha 1-antitrypsin deficiency - Cystic fibrosis - Amyloidosis (Familial Mediterranean fever) - Acatalasia |
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| Pathology: Immune disorders (primarily D80-D89, 273, 279) |
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| Antibody defects | X-linked agammaglobulinemia - Selective immunoglobulin A deficiency |
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| Combined immunodeficiencies | Severe combined immunodeficiency (X-SCID) - Adenosine deaminase deficiency - Nezelof syndrome - Purine nucleoside phosphorylase deficiency - Bare lymphocyte syndrome |
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| Other | Wiskott-Aldrich syndrome - DiGeorge syndrome - Hyper-IgE syndrome - Common variable immunodeficiency - Complement deficiency (Angioedema) - Sarcoidosis - Hypergammaglobulinemia - Cryoglobulinemia - Paraproteinemia - Immunodeficiency/Primary immunodeficiency |
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| Autoimmunity | see list of autoimmune diseases |
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