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)

• Simple and unspecified goiter
• Goiter, unspec.
• Nontoxic nodular goiter
• Thyroid nodule
• Goiter, unspec. nontoxic nodular
• Thyrotoxicosis with or without goiter
• Goiter toxic, diffuse
• Hyperthyroidism, NOS
• Congenital hypothyroidism
• Acquired hypothyroidism
• Hypothyroidism, post-surgical
• Hypothyroidism, post-ablative
• Hypothyroidism, unspec.
• Thyroiditis
• Thyroiditis, acute
• Thyroiditis, subacute
• Thyroiditis, chronic, Hashimoto's
• Other disorders of thyroid
• Thyroid cyst

diseases of other endocrine glands (250-259)

• ''Note: for 250-259, 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
• Diabetes mellitus
• Diabetes mellitus without mention of complication
• Diabetes with ketoacidosis
• Diabetes with hyperosmolarity
• Diabetes with other coma
• Diabetes with renal manifestations
• Diabetes with ophthalmic manifestations
• Diabetes with neurological manifestations
• Diabetes with peripheral circulatory disorders
• Diabetes with other specified manifestations
• Diabetes with unspecified complication
• Other disorders of pancreatic internal secretion
• Hypoglycemia, nondiabetic, unspec.
• Disorders of parathyroid gland
• Hyperparathyroidism, unspec.
• Hyperparathyroidism, primary
• Hypoparathyroidism
• Disorders of the pituitary gland and its hypothalamic control
• Growth hormone deficiency
• SIADH
• Diseases of thymus gland
• Disorders of adrenal glands
• Cushing's syndrome
• Ovarian dysfunction
• Ovarian failure, postablative
• Ovarian failure, other
• Ovaries, polycystic
• Testicular dysfunction
• Testicular hypofunction
• Polyglandular dysfunction and related disorders
• Other endocrine disorders
• Puberty, delayed
• Sexual precocity

nutritional deficiencies (260-269)

• Kwashiorkor
• Nutritional marasmus
• Other severe protein-calorie malnutrition
• Other and unspecified protein-calorie malnutrition
• Vitamin A deficiency
• With conjunctival xerosis
• With conjunctival xerosis and Bitot's spot
• With corneal xerosis
• With corneal ulceration and xerosis
• With keratomalacia
• With night blindness
• With xerophthalmic scars of cornea
• Other ocular manifestations of vitamin A deficiency
• Other manifestations of vitamin A deficiency
• Unspecified vitamin A deficiency
• Thiamine and niacin deficiency states
• Beriberi
• Other and unspecified manifestations of thiamine deficiency
• Wernicke's encephalopathy
• Pellagra
• Deficiency of B-complex components
• Ariboflavinosis
• B12 deficiency w/o anemia
• Ascorbic acid deficiency
• Vitamin D deficiency
• Other nutritional deficiencies
• Deficiency of vitamin K
• Deficiency of other vitamins
• Unspecified vitamin deficiency
• Mineral deficiency, not elsewhere classified

other metabolic and immunity disorders (270-279)

• Disorders of amino-acid transport and metabolism
• Disturbances of amino-acid transport
• Cystinosis
• Cystinuria
• Hartnup disease
• Phenylketonuria (PKU)
• Tetrahydrobiopterin deficiency
• Other disturbances of aromatic amino-acid metabolism
• Albinism
• Alkaptonuria
• Hypertyrosinemia
• Ochronosis
• Waardenburg syndrome
• Disturbances of branched-chain amino-acid metabolism
• Isobutyryl-coenzyme A dehydrogenase deficiency
• Isovaleric acidemia
• Maple syrup urine disease
• Methylmalonic acidemia
• Propionic acidemia
• Disturbances of sulphur-bearing amino-acid metabolism
• Homocystinuria
• Disorders of histidine metabolism
• Carnosinemia
• Histidinemia
• Hyperhistidinemia
• Imidazole aminoaciduria
• Urocanic aciduria
• Disorders of urea cycle metabolism
• Citrullinemia
• Hyperammonemia
• Disorders of straight-chain amino-acid metabolism
• Hyperlysinemia
• Pipecolic acidemia
• Saccharopinuria
• Other specified disorders of amino-acid metabolism
• Trimethylaminuria

• Disorders of carbohydrate transport and metabolism
• Glycogenosis
• von Gierke's disease
• McArdle's disease
• Pompe's disease
• Galactosemia
• Hereditary fructose intolerance
• Intestinal disaccharidase deficiencies and disaccharide malabsorption
• Lactose intolerance
• Glucose intolerance
• Renal glycosuria
• Disorders of lipoid metabolism
• Pure hypercholesterolemia
• Fredrickson Type IIa hyperlipoproteinemia
• Familial hypercholesterolemia
• Pure hyperglyceridemia
• Hypertriglyceridemia, essential
• Fredrickson Type IV hyperlipoproteinemia
• Hyperlipidemia, mixed
• Fredrickson Type IIb or III hyperlipoproteinemia
• Tubo-eruptive xanthoma
• Xanthoma tuberosum
• Hyperchylomicronemia
• Bürger-Grütz syndrome
• Fredrickson type I or V hyperlipoproteinemia
• Hyperlipidemia, Group D
• Mixed hyperglyceridemia
• Other and unspecified hyperlipidemia
• Alpha-lipoproteinemia
• Combined hyperlipidemia
• Lipoprotein deficiencies
• Abetalipoproteinemia
• Bassen-Kornzweig syndrome
• High-density lipoid deficiency
• Hypoalphalipoproteinemia
• Hypobetalipoproteinemia (familial)
• Lipodystrophy
• Lipidoses
• Gaucher's disease
• Niemann-Pick disease
• Sea-blue histiocyte syndrome
• Other disorders of lipoid metabolism
• Carnitine-acylcarnitine translocase deficiency
• Mitochondrial trifunctional protein deficiency

• Disorders of plasma protein metabolism
• Polyclonal hypergammaglobulinemia
• Monoclonal paraproteinemia
• Other paraproteinemias
• Macroglobulinemia
• Waldenström macroglobulinemia
• Other disorders of plasma protein metabolism
• Atransferrinemia

• Gout
• Gouty arthropathy
• Disorders of mineral metabolism
• Disorders of iron metabolism
• Aceruloplasminemia
• Hemochromatosis
• Disorders of copper metabolism
• Wilson's disease
• Disorders of magnesium metabolism
• Hypermagnesemia
• Hypomagnesemia
• Disorders of phosphorus metabolism
• Familial hypophosphatemia
• Hypophosphatasia
• Disorders of calcium metabolism
• Hypocalcemia
• Hypercalcemia
• Pseudohypoparathyroidism
• Disorders of fluid, electrolyte, and acid-base balance
• Hypernatremia
• Hyponatremia
• Acidosis
• Alkalosis
• Mixed acid-base balance disorder
• Dehydration
• Hypovolemia
• Hyperkalemia
• Hypokalemia
• Other and unspecified disorders of metabolism
• Cystic fibrosis
• Disorders of porphyrin metabolism
• Porphyria
• Acute intermittent porphyria
• Other disorders of purine and pyrimidine metabolism
• Lesch-Nyhan syndrome
• Purine nucleoside phosphorylase deficiency
• Xanthinuria
• Amyloidosis
• Familial Mediterranean fever
• Hyperbilirubinemia
• Crigler-Najjar syndrome
• Gilbert's syndrome
• Mucopolysaccharidosis
• Hunter's syndrome
• Hurler's syndrome
• Morquio-Brailsford disease
• Sanfilippo's syndrome
• Other deficiencies of circulating enzymes
• Alpha 1-antitrypsin deficiency
• Biotinidase deficiency
• Hereditary angioedema
• Dysmetabolic syndrome x
• Metabolic syndrome
• Other specified disorders of metabolism
• Primary carnitine deficiency
• Carnitine deficiency due to inborn errors of metabolism
• Iatrogenic carnitine deficiency
• Other secondary carnitine deficiency
• 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
• Disorders of peroxisomal metabolism
• Zellweger syndrome
• 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)
• Other specified disorders of metabolism

• Obesity and other hyperalimentation
• Obesity, NOS
• Localized adiposity
• Hypervitaminosis A
• Hypercarotinemia
• Hypervitaminosis D

• Disorders involving the immune mechanism
• Deficiency of humoral immunity
• Deficiency of cell-mediated immunity
• DiGeorge syndrome
• Wiskott-Aldrich syndrome
• Combined immunity deficiency
• Severe combined immunodeficiency

See also

• List of ICD-9 codes
• ICD-10 Chapter E: Endocrine, nutritional and metabolic diseases