List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders
Chapter | Block | Title |
---|---|---|
I | 001–139 | Infectious and Parasitic Diseases |
II | 140–239 | Neoplasms |
III | 240–279 | Endocrine, Nutritional and Metabolic Diseases, and Immunity Disorders |
IV | 280–289 | Diseases of the Blood and Blood-forming Organs |
V | 290–319 | Mental Disorders |
VI | 320–389 | Diseases of the Nervous System and Sense Organs |
VII | 390–459 | Diseases of the Circulatory System |
VIII | 460–519 | Diseases of the Respiratory System |
IX | 520–579 | Diseases of the Digestive System |
X | 580–629 | Diseases of the Genitourinary System |
XI | 630–679 | Complications of Pregnancy, Childbirth, and the Puerperium |
XII | 680–709 | Diseases of the Skin and Subcutaneous Tissue |
XIII | 710–739 | Diseases of the Musculoskeletal System and Connective Tissue |
XIV | 740–759 | Congenital Anomalies |
XV | 760–779 | Certain Conditions originating in the Perinatal Period |
XVI | 780–799 | Symptoms, Signs and Ill-defined Conditions |
XVII | 800–999 | Injury and Poisoning |
E800–E999 | Supplementary Classification of External Causes of Injury and Poisoning | |
V01–V82 | Supplementary Classification of Factors influencing Health Status and Contact with Health Services | |
Morphology of Neoplasms |
This is a shortened version of the third chapter of the ICD-9: Endocrine, Nutritional and Metabolic Diseases, and Immunity Disorders. It covers ICD codes 240 to 279. The full chapter can be found on pages 145 to 165 of Volume 1, which contains all (sub)categories of the ICD-9. Volume 2 is an alphabetical index of Volume 1. Both volumes can be downloaded for free from the website of the World Health Organization.
Disorders of thyroid gland (240–246)[]
- 240 Simple and unspecified goiter
- 240.9 Goiter, unspec.
- 241 Nontoxic nodular goiter
- 242 Thyrotoxicosis with or without goiter
- 243 Congenital hypothyroidism
- 244
- 245 Thyroiditis
- 245.0 Thyroiditis, acute
- 245.1 Thyroiditis, subacute
- 245.2 Thyroiditis, chronic, Hashimoto's
- 246 Other disorders of thyroid
- 246.2 Thyroid cyst
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
- 249.8 Secondary
- 249.9 Secondary
- 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
- 250.8
- 250.9
- 251 Other disorders of
- 251.2 Hypoglycemia, nondiabetic, unspec.
- 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
- 257
- 258 and related disorders
- 259 Other endocrine disorders
- 259.0 Puberty, delayed
- 259.1 Sexual precocity
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
- 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
- Cystinosis
- Cystinuria
- Hartnup disease
- 270.1 Phenylketonuria (PKU)
- 270.1 Tetrahydrobiopterin deficiency
- 270.2 Other disturbances of aromatic amino-acid metabolism
- Albinism
- Alkaptonuria
- Hypertyrosinemia
- Ochronosis
- Waardenburg syndrome
- 270.3 Disturbances of branched-chain amino-acid metabolism
- Isobutyryl-coenzyme A dehydrogenase deficiency
- Isovaleric acidemia
- Maple syrup urine disease
- Methylmalonic acidemia
- Propionic acidemia
- 270.4 Disturbances of sulphur-bearing amino-acid metabolism
- Homocystinuria
- 270.5 Disorders of histidine metabolism
- Carnosinemia
- Histidinemia
- Urocanic aciduria
- 270.6 Disorders of urea cycle metabolism
- Citrullinemia
- Hyperammonemia
- 270.7 Disorders of straight-chain amino-acid metabolism
- 270.8 Other specified disorders of amino-acid metabolism
- Trimethylaminuria
- 270.0 Disturbances of amino-acid transport
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
- Lactose intolerance
- Glucose intolerance
- 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
- Fredrickson Type IIa hyperlipoproteinemia
- Familial hypercholesterolemia
- 272.1 Pure hyperglyceridemia
- Hypertriglyceridemia, essential
- Fredrickson Type IV hyperlipoproteinemia
- 272.2 Hyperlipidemia, mixed
- Fredrickson Type IIb or III hyperlipoproteinemia
- Tubo-eruptive xanthoma
- Xanthoma tuberosum
- 272.3 Hyperchylomicronemia
- Bürger-Grütz syndrome
- Fredrickson type I or V hyperlipoproteinemia
- Hyperlipidemia, Group D
- 272.4 Other and unspecified hyperlipidemia
- Combined hyperlipidemia
- 272.5 Lipoprotein deficiencies
- Abetalipoproteinemia
- Bassen-Kornzweig syndrome
- Hypoalphalipoproteinemia
- Hypobetalipoproteinemia (familial)
- 272.6 Lipodystrophy
- 272.7 Lipidoses
- Gaucher's disease
- Niemann-Pick disease
- Sea-blue histiocyte syndrome
- 272.8 Other disorders of lipoid metabolism
- 272.0 Pure hypercholesterolemia
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
- Atransferrinemia
Gout[]
Disorders of mineral metabolism[]
- 275 Disorders of
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
- Porphyria
- Acute intermittent porphyria
- Porphyria
- 277.2 Other disorders of purine and pyrimidine metabolism
- Lesch–Nyhan syndrome
- Purine nucleoside phosphorylase deficiency
- Xanthinuria
- 277.3 Amyloidosis
- 277.4 Hyperbilirubinemia
- 277.5 Mucopolysaccharidosis
- Hunter syndrome
- Hurler syndrome
- Morquio–Brailsford disease
- Sanfilippo syndrome
- 277.6 Other deficiencies of circulating enzymes
- Alpha 1-antitrypsin deficiency
- Biotinidase deficiency
- Hereditary angioedema
- 277.7
- Metabolic syndrome
- 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
- Carnitine palmitoyltransferase I deficiency
- Carnitine palmitoyltransferase II deficiency
- Very long-chain acyl-coenzyme A dehydrogenase deficiency
- Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
- Medium-chain acyl-coenzyme A dehydrogenase deficiency
- 277.86 Disorders of peroxisomal metabolism
- Zellweger syndrome
- 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
Disorders involving the immune mechanism[]
- 279 Disorders involving the immune mechanism
- 279.0 Deficiency of humoral immunity
- 279.1 Deficiency of cell-mediated immunity
- 279.2 Combined immunity deficiency
- Severe combined immunodeficiency
- 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
Categories:
- International Classification of Diseases