Endocrine, nutritional and metabolic diseases, and immunity disorders: Encyclopedia with 57,945 entries from biotech, medicine & life sciences.

List of ICD-9 codes 240-279: Endocrine, nutritional and metabolic diseases, and immunity disorders

1 3. Endocrine, nutritional and metabolic diseases, and immunity disorders (240-279)
2 See also

3. Endocrine, nutritional and metabolic diseases, and immunity disorders (240-279)

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 (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
(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 classified

other metabolic and immunity disorders (270-279)

(270) Disorders of amino-acid transport and metabolism
- (270.0) Disturbances of amino-acid transport
- (270.1) Phenylketonuria (PKU)
- (270.2) Other disturbances of aromatic amino-acid metabolism
  - Albinism
  - Alkaptonuria
  - Hypertyrosinemia
  - Ochronosis
  - Waardenburg syndrome
- (270.3) Disturbances of branched-chain amino-acid metabolism
  - Maple syrup urine disease
- (270.4) Disturbances of sulphur-bearing amino-acid metabolism
  - Homocystinuria
- (270.6) Disorders of urea cycle metabolism
  - Citrullinemia
  - Hyperammonemia
- (270.8) Other specified disorders of amino-acid metabolism
  - Trimethylaminuria

(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
(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
  - Bassen-Kornzweig syndrome
  - High-density lipoid deficiency
  - Hypoalphalipoproteinemia
  - Hypobetalipoproteinemia (familial)
- (272.6) Lipodystrophy
- (272.7) Lipidoses
- (272.8) Other disorders of lipoid metabolism
  - Carnitine-acylcarnitine translocase deficiency
  - Mitochondrial trifunctional protein deficiency

(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
- (275.0) Disorders of iron metabolism
  - 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
(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
(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
  - Xanthinuria
- (277.3) Amyloidosis
  - Familial Mediterranean fever
- (277.4) Hyperbilirubinemia
  - Crigler-Najjar syndrome
  - Gilbert's syndrome
- (277.5) Mucopolysaccharidosis
- (277.6) Other deficiencies of circulating enzymes
  - Alpha 1-antitrypsin 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
  - (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)
  - (277.89) Other specified 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

v • d • e Endocrine pathology: endocrine diseases (E00-35, 240-259)
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
Pancreas	Diabetes mellitus (type 1, type 2, coma, angiopathy, ketoacidosis, nephropathy, neuropathy, retinopathy) - Hypoglycemia - Hyperinsulinism - Zollinger-Ellison syndrome
Parathyroid	Hypoparathyroidism (Pseudohypoparathyroidism) - Hyperparathyroidism (Primary, Secondary, Tertiary)
Pituitary	Hyperpituitarism (Acromegaly, Hyperprolactinaemia, SIADH) - Hypopituitarism (Simmonds' disease/Sheehan's syndrome, Kallmann syndrome, Growth hormone deficiency, Diabetes insipidus) - Adiposogenital dystrophy - Empty sella syndrome
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
Gonads	ovarian dysfunction (Polycystic ovary syndrome, Premature ovarian failure) - testicular dysfunction (5-alpha-reductase deficiency) - general (Hypogonadism, Delayed puberty, Precocious puberty)
Other	Autoimmune polyendocrine syndrome - Carcinoid syndrome - Short stature (Laron syndrome, Psychogenic dwarfism) - Gigantism - Androgen insensitivity syndrome - Progeria - Multiple endocrine neoplasia (1, 2)

v • d • e Nutritional pathology (E40-68, 260-269)
Malnutrition	Kwashiorkor - Marasmus
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
Hyperalimentation	Obesity - Hypervitaminosis A - Hypervitaminosis D

v • d • e Metabolic pathology / Inborn error of metabolism (E70-90, 270-279)
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
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
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)
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)
Mineral	Cu Wilson's disease/Menkes disease - Fe Haemochromatosis - Zn Acrodermatitis enteropathica - PO₄^3�' Hypophosphatemia/Hypophosphatasia - Mg²⁺ Hypermagnesemia/Hypomagnesemia - Ca²⁺ Hypercalcaemia/Hypocalcaemia/Disorders of calcium metabolism
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
Purine and pyrimidine	Hyperuricemia - Lesch-Nyhan syndrome - Xanthinuria
Porphyrin	Acute intermittent, Gunther's, Cutanea tarda, Erythropoietic, Hepatoerythropoietic, Hereditary copro-, Variegate
Bilirubin	Unconjugated (Lucey-Driscoll syndrome, Gilbert's syndrome, Crigler-Najjar syndrome) - Conjugated (Dubin-Johnson syndrome, Rotor syndrome)
Glycosaminoglycan	Mucopolysaccharidosis - 1:Hurler/Hunter - 3:Sanfilippo - 4:Morquio - 6:Maroteaux-Lamy - 7:Sly
Glycoprotein	Mucolipidosis - I-cell disease - Pseudo-Hurler polydystrophy - Aspartylglucosaminuria - Fucosidosis - Alpha-mannosidosis - Sialidosis
Other	Alpha 1-antitrypsin deficiency - Cystic fibrosis - Amyloidosis (Familial Mediterranean fever) - Acatalasia

v • d • e Pathology: Immune disorders (primarily D80-D89, 273, 279)
Antibody defects	X-linked agammaglobulinemia - Selective immunoglobulin A deficiency
Combined immunodeficiencies	Severe combined immunodeficiency (X-SCID) - Adenosine deaminase deficiency - Nezelof syndrome - Purine nucleoside phosphorylase deficiency - Bare lymphocyte syndrome
Other	Wiskott-Aldrich syndrome - DiGeorge syndrome - Hyper-IgE syndrome - Common variable immunodeficiency - Complement deficiency (Angioedema) - Sarcoidosis - Hypergammaglobulinemia - Cryoglobulinemia - Paraproteinemia - Immunodeficiency/Primary immunodeficiency
Autoimmunity	see list of autoimmune diseases

Category: Metabolic disorders

This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "List_of_ICD-9_codes_240-279:_Endocrine,_nutritional_and_metabolic_diseases,_and_immunity_disorders". A list of authors is available in Wikipedia.

Life Science Encyclopedia

Contents

3. Endocrine, nutritional and metabolic diseases, and immunity disorders (240-279)

disorders of thyroid gland (240-246)

diseases of other endocrine glands (250-259)

nutritional deficiencies (260-269)

other metabolic and immunity disorders (270-279)

See also