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"Control of Communicable Diseases Manual"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
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  • tuberculosis control
    °áÇÙ°ü¸®.
  • tuberculosis control
    °áÇÙ¿¹¹æ(Ë­Ì´ËçËÑ), °áÇÙ°ü¸®.
  • tumor control
    Á¾¾ç¾ïÁ¦
  • tumor control dose
    Á¾¾ç¾ïÁ¦¼±·®
  • tumor control probability, TCP
    Á¾¾ç¾ïÁ¦¿ï
  • venereal disease control
    ¼ºº´°ü¸®.
  • vestibuloequilibratory control
    ÀüÁ¤ÆòÇüÁ¶Àý(¡­øÁû¬ðàï½).
  • volitional control
    ÀÚ¹ßÀû Á¦¾î(¡­îÜð¤åÙ).
  • water pollution control
    ¼öÁú¿À¿°±ÔÁ¦(Ëà̤ËçËç˻̡).
  • water quality control
    ¼öÁú°ü¸®(Ëà̤˴Ëö).
  • weed control =weedicide
    ÀâÃʹæÁ¦(Ëö̧ËÑÌ¡).
  • weight control programs
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NIADDK National Institute of Arthritis, Diabetes, Digestive and Kidney Diseases
NIAID National Institute of Allergy and Infectious Diseases
NIAMDD National Institute of Arthritis, Metabolism, and Digestive Diseases
NIAMS National Institute of Arthritis, Musculoskeletal and Skin Diseases
NINCDS/ADRDA National Institute of Neurological and Communicative Diseases and Stroke/Alzheimer's Disease and Rel...
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Cn Control
CG Control Group
C Group Control group
CON Control subjects
CCP critical control point
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sexually transmitted diseases, viral Viral diseases which are transmitted or propagated by sexual conduct.
(12 Dec 1998)
sheep diseases Diseases of domestic and mountain sheep of the genus ovis.
(12 Dec 1998)
single-gene diseases Hereditary disorders caused by a change (mutation) in a single gene. There are thousands of single-gene diseases including achondroplastic dwarfism, huntington disease, cystic fibrosis, sickle cell disease, duchenne muscular dystrophy, and haemophilia. Single-gene diseases typically describe classic simple mendelian patterns of inheritance (as autosomal dominant, autosomal recessive, and x-linked traits) by comparison with polygenic diseases.
(12 Dec 1998)
skin and connective tissue diseases A collective term for diseases of the skin and its appendages and of connective tissue.
(12 Dec 1998)
skin diseases, bacterial Skin diseases caused by bacteria.
(12 Dec 1998)
skin diseases, eczematous Any of a variety of eruptive skin disorders characterised by erythema, oozing, vesiculation, and scaling. Aetiology is varied.
(12 Dec 1998)
skin diseases, genetic Diseases of the skin with a genetic component, usually the result of various inborn errors of metabolism.
(12 Dec 1998)
skin diseases, infectious Skin diseases caused by bacteria, fungi, parasites, or viruses.
(12 Dec 1998)
skin diseases, metabolic Diseases of the skin associated with underlying metabolic disorders.
(12 Dec 1998)
skin diseases, papulosquamous A group of dermatoses with distinct morphologic features. The primary lesion is most commonly a papule, usually erythematous, with a variable degree of scaling on the surface. Plaques form through the coalescing of primary lesions.
(12 Dec 1998)
skin diseases, parasitic Skin diseases caused by arthropods, helminths, or protozoa.
(12 Dec 1998)
skin diseases, vascular Skin diseases affecting or involving the cutaneous blood vessels and generally manifested as inflammation, swelling, erythema, or necrosis in the affected area.
(12 Dec 1998)
skin diseases, vesiculobullous Skin diseases characterised by local or general distributions of blisters. They are classified according to the site and mode of blister formation. Lesions can appear spontaneously or be precipitated by infection, trauma, or sunlight. Aetiologies include immunologic and genetic factors.
(12 Dec 1998)
skin diseases, viral Skin diseases caused by viruses.
(12 Dec 1998)
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)
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