International Cla**ification of Diseases - Endocrine, Nutritional and Metabolic Diseases, and Immunity Disorders (240-279) lyrics

Disorders of thyroid gland (240–246) (240) Simple and unspecified goiter (240.9) Goiter, unspec. (241) Nontoxic nodular goiter (241.0) Thyroid nodule (241.9) Goiter, unspec. nontoxic nodular (242) Thyrotoxicosis with or without goiter (242.0) Goiter toxic, diffuse (242.9) Hyperthyroidism, NOS (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 (246.2) Thyroid cyst Diseases of other endocrine glands (249–259) (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 (251.2) Hypoglycemia, nondiabetic, unspec. (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 (253.3) Growth hormone deficiency (253.6) SIADH (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 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 (265.0) Beriberi (265.1) Other and unspecified manifestations of thiamine deficiency -Wernicke's encephalopathy (265.2) Pellagra (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 cla**ified 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 -h*mocystinuria (270.5) Disorders of histidine metabolism -Carnosinemia -Histidinemia -Hyperhistidinemia -Imidazole aminoaciduria -Urocanic aciduria (270.6) Disorders of urea cycle metabolism -Citrullinemia -Hyperammonemia (270.7) Disorders of straight-chain amino-acid metabolism -Hyperlysinemia -Pipecolic acidemia -Saccharopinuria (270.8) Other specified disorders of amino-acid metabolism -Trimethylaminuria Disorders of carbohydrate transport and metabolism (271) Disorders of carbohydrate transport and metabolism (271.0) Glycogenosis -von Gierke's disease -McArdle's disease -Pompe's disease (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 -Mixed hyperglyceridemia (272.4) Other and unspecified hyperlipidemia -Alpha-lipoproteinemia -Combined hyperlipidemia (272.5) Lipoprotein deficiencies -Abetalipoproteinemia -Ba**en-Kornzweig syndrome -High-density lipoid deficiency -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 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 -Waldenström macroglobulinemia (273.8) Other disorders of plasma protein metabolism -Atransferrinemia (274) Gout (274.0) Gouty arthropathy Disorders of mineral metabolism (275) Disorders of mineral metabolism (275.0) Disorders of iron metabolism -Aceruloplasminemia -Hemochromatosis (275.1) Disorders of copper metabolism -Wilson's disease (275.2) Disorders of magnesium metabolism -Hypermagnesemia -Hypomagnesemia (275.3) Disorders of phosphorus metabolism -Familial hypophosphatemia -Hypophosphatasia (275.4) Disorders of calcium metabolism (275.41) Hypocalcemia (275.42) Hypercalcemia (275.49) Pseudohypoparathyroidism Disorders of fluid, electrolyte, and acid-base balance (276) Disorders of fluid, electrolyte, and acid-base balance (276.0) Hypernatremia (276.1) Hyponatremia (276.2) Acidosis (276.3) Alkalosis (276.4) Mixed acid-base balance disorder (276.5) Dehydration (276.52) Hypovolemia (276.7) Hyperkalemia (276.8) Hypokalemia 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 (277.2) Other disorders of purine and pyrimidine metabolism -Lesch-Nyhan syndrome -Purine nucleoside phosphorylase deficiency -Xanthinuria (277.3) Amyloidosis -Familial Mediterranean fever (277.4) Hyperbilirubinemia -Crigler-Najjar syndrome -Gilbert's syndrome (277.5) Mucopolysaccharidosis -Hunter's syndrome -Hurler's syndrome -Morquio-Brailsford disease -Sanfilippo's syndrome (277.6) Other deficiencies of circulating enzymes -Alpha 1-antitrypsin deficiency -Biotinidase deficiency -Hereditary angioedema (277.7) Dysmetabolic syndrome x -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 (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 -Severe combined immunodeficiency (279.3) Unspecified immunity deficiency (279.4) Autoimmune disease not elsewhere cla**ified (279.5) Graft-versus-host disease (279.8) Other specified disorders involving the immune mechanism (279.9) Unspecified disorder of immune mechanism