List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders
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
- (245) Thyroiditis
- (246) Other disorders of thyroid
Diseases of other endocrine glands (249–259)
- Note: for 249–259, the following fifth digit can be added:
- (250.x0) Diabetes mellitus type 2
- (250.x1) Diabetes mellitus type 1
- (250.x2) Diabetes mellitus type 2, uncontrolled
- (250.x3) Diabetes mellitus type 1, uncontrolled
- (249) Secondary diabetes mellitus
- (249.0) Secondary diabetes mellitus without mention of complication
- (249.1) Secondary diabetes mellitus with ketoacidosis
- (249.2) Secondary diabetes mellitus with hyperosmolarity
- (249.3) Secondary diabetes mellitus with other coma
- (249.4) Secondary diabetes mellitus with renal manifestations
- (249.5) Secondary diabetes mellitus with ophthalmic manifestations
- (249.6) Secondary diabetes mellitus with neurological manifestations
- (249.7) Secondary diabetes mellitus with peripheral circulatory disorders
- (249.8) Secondary diabetes mellitus with other specified manifestations
- (249.9) Secondary diabetes mellitus with unspecified complications
- (250) Diabetes mellitus
- (250.0) Diabetes mellitus without mention of complication
- (250.1) Diabetes with ketoacidosis
- (250.2) Diabetes with hyperosmolarity
- (250.3) Diabetes with other coma
- (250.4) Diabetes with renal manifestations
- (250.5) Diabetes with ophthalmic manifestations
- (250.6) Diabetes with neurological manifestations
- (250.7) Diabetes with peripheral circulatory disorders
- (250.8) Diabetes with other specified manifestations
- (250.9) Diabetes with unspecified complication
- (251) Other disorders of pancreatic internal secretion
- (252) Disorders of parathyroid gland
- (253) Disorders of the pituitary gland and its hypothalamic control
- (254) Diseases of thymus gland
- (255) Disorders of adrenal glands
- (256) Ovarian dysfunction
- (256.2) Ovarian failure, postablative
- (256.39) Ovarian failure, other
- (256.4) Ovaries, polycystic
- (256.2) Ovarian failure, postablative
- (257) Testicular dysfunction
- (257.2) Testicular hypofunction
- (258) Polyglandular dysfunction and related disorders
- (259) Other endocrine disorders
Nutritional deficiencies (260–269)
- (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
- (266) Deficiency of B-complex components
- (266.0) Ariboflavinosis
- (266.2) B12 deficiency w/o anemia
- (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)
Disorders of amino-acid transport and metabolism
- (270) Disorders of amino-acid transport and metabolism
- (270.0) Disturbances of amino-acid transport
- (270.1) Phenylketonuria (PKU)
- (270.1) Tetrahydrobiopterin deficiency
- (270.2) Other disturbances of aromatic amino-acid metabolism
- (270.3) Disturbances of branched-chain amino-acid metabolism
- (270.4) Disturbances of sulphur-bearing amino-acid metabolism
- (270.5) Disorders of histidine metabolism
- Carnosinemia
- Histidinemia
- Hyperhistidinemia
- Imidazole aminoaciduria
- Urocanic aciduria
- (270.6) Disorders of urea cycle metabolism
- (270.7) Disorders of straight-chain amino-acid metabolism
- (270.8) Other specified disorders of amino-acid metabolism
Disorders of carbohydrate transport and metabolism
- (271) Disorders of carbohydrate transport and metabolism
- (271.0) Glycogenosis
- (271.1) Galactosemia
- (271.2) Hereditary fructose intolerance
- (271.3) Intestinal disaccharidase deficiencies and disaccharide malabsorption
- (271.4) Renal glycosuria
- (271.8) Other specified disorders of carbohydrate transport and metabolism
- (271.9) Unspecified disorder of carbohydrate transport and metabolism
Disorders of lipoid metabolism
- (272) Disorders of lipoid metabolism
- (272.0) Pure hypercholesterolemia
- (272.1) Pure hyperglyceridemia
- (272.2) Hyperlipidemia, mixed
- (272.3) Hyperchylomicronemia
- Bürger-Grütz syndrome
- Fredrickson type I or V hyperlipoproteinemia
- Hyperlipidemia, Group D
- Mixed hyperglyceridemia
- (272.4) Other and unspecified hyperlipidemia
- Alpha-lipoproteinemia
- Combined hyperlipidemia
- (272.5) Lipoprotein deficiencies
- Abetalipoproteinemia
- Bassen-Kornzweig syndrome
- High-density lipoid deficiency
- Hypoalphalipoproteinemia
- Hypobetalipoproteinemia (familial)
- (272.6) Lipodystrophy
- (272.7) Lipidoses
- (272.8) Other disorders of lipoid metabolism
Disorders of plasma protein metabolism
- (273) Disorders of plasma protein metabolism
- (273.0) Polyclonal hypergammaglobulinemia
- (273.1) Monoclonal paraproteinemia
- (273.2) Other paraproteinemias
- (273.3) Macroglobulinemia
- (273.8) Other disorders of plasma protein metabolism
Gout
Disorders of mineral metabolism
- (275) Disorders of mineral metabolism
- (275.0) Disorders of iron metabolism
- (275.1) Disorders of copper metabolism
- (275.2) Disorders of magnesium metabolism
- (275.3) Disorders of phosphorus metabolism
- Familial hypophosphatemia
- Hypophosphatasia
- (275.4) Disorders of calcium metabolism
Disorders of fluid, electrolyte, and acid-base balance
- (276) Disorders of fluid, electrolyte, and acid-base balance
Other and unspecified disorders of metabolism
- (277) Other and unspecified disorders of metabolism
- (277.0) Cystic fibrosis
- (277.1) Disorders of porphyrin metabolism
- (277.2) Other disorders of purine and pyrimidine metabolism
- (277.3) Amyloidosis
- (277.4) Hyperbilirubinemia
- (277.5) Mucopolysaccharidosis
- (277.6) Other deficiencies of circulating enzymes
- (277.7) Dysmetabolic syndrome x
- (277.8) Other specified disorders of metabolism
- (277.81) Primary carnitine deficiency
- (277.82) Carnitine deficiency due to inborn errors of metabolism
- (277.83) Iatrogenic carnitine deficiency
- (277.84) Other secondary carnitine deficiency
- (277.85) Disorders of fatty acid oxidation metabolism
- (277.86) Disorders of peroxisomal metabolism
- (277.87) Disorders of mitochondrial metabolism
- Kearns-Sayre syndrome
- Mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS syndrome)
- Mitochondrial neurogastrointestinal encephalopathy syndrome (MNGIE)
- Myoclonus with epilepsy and with ragged red fibers (MERRF syndrome)
- Neuropathy, ataxia, and retinitis pigmentosa (NARP syndrome)
- (277.88) Tumor lysis syndrome
- (277.89) Other specified disorders of metabolism
Obesity and other hyperalimentation
- (278) Obesity and other hyperalimentation
- (278.0) Obesity, NOS
- (278.1) Localized adiposity
- (278.2) Hypervitaminosis A
- (278.3) Hypercarotinemia
- (278.4) Hypervitaminosis D
Disorders involving the immune mechanism
- (279) Disorders involving the immune mechanism
- (279.0) Deficiency of humoral immunity
- (279.00) Hypogammaglobulinemia unspecified
- (279.01) Selective IgA immunodeficiency
- (279.02) Selective IgM immunodeficiency
- (279.03) Other selective immunoglobulin deficiencies
- (279.04) Congenital hypogammaglobulinemia
- (279.05) Immunodeficiency with increased IgM
- (279.06) Common variable immunodeficiency
- (279.09) Other deficiency of humoral immunity
- (279.1) Deficiency of cell-mediated immunity
- (279.10) Immunodeficiency with predominant t-cell defect unspecified
- (279.11) DiGeorge syndrome
- (279.12) Wiskott-Aldrich syndrome
- (279.13) Nezelof's syndrome
- (279.19) Other deficiency of cell-mediated immunity
- (279.2) Combined immunity deficiency
- (279.3) Unspecified immunity deficiency
- (279.4) Autoimmune disease not elsewhere classified
- (279.5) Graft-versus-host disease
- (279.8) Other specified disorders involving the immune mechanism
- (279.9) Unspecified disorder of immune mechanism
- (279.0) Deficiency of humoral immunity
See also
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