Assessment |
Biopsychology |
Comparative |
Cognitive |
Developmental |
Language |
Individual differences |
Personality |
Philosophy |
Social |
Methods |
Statistics |
Clinical |
Educational |
Industrial |
Professional items |
World psychology |
Biological: Behavioural genetics · Evolutionary psychology · Neuroanatomy · Neurochemistry · Neuroendocrinology · Neuroscience · Psychoneuroimmunology · Physiological Psychology · Psychopharmacology (Index, Outline)
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
- (241.0) Thyroid nodule
- (241.9) Goiter, unspec. nontoxic nodular
- (242) Thyrotoxicosis with or without goiter
- (243) Congenital hypothyroidism
- (244) Acquired hypothyroidism
- (245) Thyroiditis
- (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
- (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
- (267) Ascorbic acid deficiency
- (268) Vitamin D deficiency
- (269) Other nutritional deficiencies
other metabolic and immunity disorders (270-279)[]
- (270) Disorders of amino-acid transport and metabolism
- (270.0) Disturbances of amino-acid transport
- Cystinosis
- Cystinuria
- Hartnup disease
- (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
- (270.4) Disturbances of sulphur-bearing amino-acid metabolism
- (270.6) Disorders of urea cycle metabolism
- Citrullinemia
- Hyperammonemia
- (270.0) Disturbances of amino-acid transport
- (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
- (271.0) Glycogenosis
- (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
- (272.0) Pure hypercholesterolemia
- (273) Disorders of plasma protein metabolism
- (274) Gout
- (274.0) Gouty arthropathy
- (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
- (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
- (276.7) Hyperkalemia
- (276.8) Hypokalemia
- (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
- Lesch-Nyhan syndrome
- Xanthinuria
- (277.3) Amyloidosis
- (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
- Hereditary angioedema
- (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
- (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
- (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
See also[]
| This page uses Creative Commons Licensed content from Wikipedia (view authors). |