| NTOS | neurogenic thoracic outlet syndrome |
|---|---|
| RITA | Randomised Intervention Treatment of Angina [UK]; right internal thoracic artery |
| STSA | Southern Thoracic Surgical Association |
| T1-T12 | first to twelfth thoracic vertebrae |
| TAA | thioacetamide; thoracic aortic aneurysm; total ankle arthroplasty; transverse aortic arch; tumor-ass... |
| APACHE II | Acute Physiology And Chronic Health Evaluation |
|---|---|
| APACHE II | Acute Physiology and Chronic Health Evaluation II |
| ABLES | Adult Blood Lead Epidemiology and Surveillance program |
| NASA | Aeronautic and Space Administration |
| AHCPR | Agency for Health Care Policy and Research |
| slow virus diseases | Diseases of viral origin, characterised by incubation periods of months to years, insidious onset of clinical manifestations, and protracted clinical course. Though the disease process is protracted, viral multiplication may not be unusually slow. Conventional viruses produce slow virus diseases such as subacute sclerosing panencephalitis, progressive multifocal leukoencephalopathy (leukoencephalopathy, progressive multifocal), and aids. Diseases produced by unconventional agents were originally considered part of this group. They are now called prion diseases. (12 Dec 1998) |
|---|---|
| social diseases | An obsolete term used to designate venereal disease's, especially gonorrhoea and syphilis. (05 Mar 2000) |
| nail diseases | Diseases of the nail plate and tissues surrounding it. The concept is limited to primates. (12 Dec 1998) |
| nasopharyngeal diseases | General or unspecified diseases of the nasopharynx. (12 Dec 1998) |
| stomatognathic diseases | General or unspecified diseases of the stomatognathic system, comprising the mouth, teeth, jaws, and pharynx. (12 Dec 1998) |
| neurodegenerative diseases | A varied assortment of central nervous system disorders characterised by gradual and progressive loss of neural tissue. (cecil textbook of medicine, 20th ed, p2050) (12 Dec 1998) |
| nose diseases | Disorders of the nose, general or unspecified. (12 Dec 1998) |
| deficiency diseases | A condition produced by dietary or metabolic deficiency. The term includes all diseases caused by an insufficient supply of essential nutrients, i.e., protein (or amino acids), vitamins, and minerals. It also includes an inadequacy of calories. (12 Dec 1998) |
| sweat gland diseases | Diseases of the sweat glands. (12 Dec 1998) |
| demyelinating diseases | Any condition characterised by the destruction of myelin and extensive loss of the myelin sheaths of the nerve fibres. It affects both the central and peripheral nervous systems. Its aetiology is at present unknown. (12 Dec 1998) |
| swine diseases | Diseases of domestic swine and of the wild boar of the genus sus. (12 Dec 1998) |
| systemic autoimmune diseases | A group of connective tissue disease's characterised by the presence of autoantibodies responsible for immunopathologically mediated tissue lesions; systemic lupus erythematosus is the prototype. (05 Mar 2000) |
| systemic febrile diseases | Generic term for diseases characterised by fever. (05 Mar 2000) |
| diseases, obesity-related | Obesity increases the risk of developing a number of diseases including: Type 2 (adult-onset) diabetes High blood pressure (hypertension) Stroke (cerebrovascular accident or CVA) Heart attack (myocardial infarction or MI) Heart failure (congestive heart failure) Cancer (only certain forms such as prostate and colon cancer) Gallstones and gall bladder disease (cholecystitis) Gout and gouty arthritis Osteoarthritis (degenerative arthritis) of the knees, hips, and the lower back Sleep apnea (failure to breath normally during sleep, lowering blood oxygen) Pickwickian syndrome (obesity, red face, underventilation, and drowsiness). (12 Dec 1998) |
| diseases, polygenic | Genetic disorders that are caused by the combined action of more than one gene. Examples of polygenic conditions include hypertension, coronary heart disease, diabetes, and peptic ulcers. Because such disorders depend on the simultaneous presence of several genes, they are not inherited as simply as single-gene diseases. (12 Dec 1998) |