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À̰ÍÀ» ¿øÇϼ̽À´Ï±î?
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  • ¿µ¹®
    ÇѱÛ
  • disease susceptibility
    Áúº´°¨¼ö¼º
  • disease taxonomy
    Áúº´ºÐ·ùÇÐ
  • extramammary Paget disease
    À¯¹æ¿ÜÆÄÁ¦Æ®º´
  • extrapyramidal disease
    ÇǶó¹Ìµå¹Ù±ù±æº´, Ãßü¿Ü·Îº´
  • endemic disease
    dzÅ亴, Áö¹æÀ¯Çິ
  • enzootic disease
    µ¿¹°Áö¹æº´, µ¿¹°ÅäÂøº´
  • epidemic disease
    À¯Çິ
  • Fabry disease
    ÆÄºê¸®º´
  • febrile disease
    ¿­º´
  • fibrocystic disease
    ¼¶À¯³¶º´
  • fifth disease
    Á¦5º´, °¨¿°È«¹Ý
  • Fahr disease
    ÆÄ¸£º´
  • fluke disease
    ÈíÃæº´
  • foot process disease
    ¹ßµ¹±âº´
  • foot-and-mouth disease
    ÀԹߺ´, ±¸Á¦¿ª
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  • ¿µ¹®
    ÇѱÛ
  • digestive tract disease
    ¼ÒÈ­°üº´
  • disease detection
    Áúº´¹ß°ß
  • disease entity
    Áúº´´ÜÀ§, Áúº´¸í
  • disease potential
    Áúº´ÀáÀç·Â
  • disease registry
    Áúº´µî·Ïü°è
  • disease susceptibility
    Áúº´°¨¼ö¼º
  • disease taxonomy
    Áúº´ºÐ·ùÇÐ
  • disease vector
    Áúº´¸Å°³Ã¼
  • disease free survival
    ¹«º´»ýÁ¸
  • disease frequency survey
    Áúº´ºóµµÁ¶»ç
  • disease odds ratio
    Áúº´±³Â÷ºñ
  • dust disease
    ¸ÕÁöº´
  • endemic disease
    dzÅ亴
  • enzootic disease
    µ¿¹°ÅäÂøº´
  • epidemic disease
    À¯Çິ
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  • ¿µ¹®
    ÇѱÛ
  • Fabrys disease
    ÆÄºê¸®º´.
  • Fabrys disease
    ÆÄºê¸®º´
  • Farber s disease
    ÆÄ¾Æ¹öº´.
  • Fordyce s disease
    Æ÷¿À´ÙÀ̽ºº´.
  • Fordyces disease
    Æ÷´ÙÀ̽ºº´
  • Fordyces disease
    Æ÷¿À´ÙÀ̽ºº´
  • Fox Fordyce disease
    Æø½º-Æ÷´ÙÀ̽ºº´
  • Gauchers disease
    °í¼Îº´
  • Gerstmann-Strauissler-Scheinker disease(GSS)
    °Ô¸£½ºÆ®¸¸ ½´Åõ·ÎÀ̽½·¯ »þÀ×Ä¿ º´
  • Gilchrist disease
    ±æÅ©¸®½ºÆ®º´
  • Gilchrists disease => North American blastomycosis
    ºÏ¾Æ¸Þ¸®Ä« ºÐ¾Æ Áø±ÕÁõ
  • Graves disease
    ±×·¹À̺꽺 º´
  • Graves disease
    ±×·¹À̺꾾º´(Ü»)
  • Graves disease
    ±×¶óºê½ºº´
  • Graves disease
    ±×·¹À̺꽺º´
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  • ¿µ¹®
    ÇѱÛ
  • dietary deficiency
    ½ÄÀ̼º ¿µ¾ç°áÇÌ(½ÄÀ̼º¿µ¾ç°áÇÌ).
  • dietary deficiency
    ½ÄÀ̼º ¿µ¾ç°áÇÌ(ãÝìÈàõç½å×ÌÀù¹).
  • diphosphatase deficiency
    µðÆ÷½ºÆÄŸÁ¦°áÇÌ(Áõ)
  • disaccaridase deficiency
    ÀÌ´çºÐÇØÈ¿¼Ò°áÇÌ(ì£ÓØÝÂú°ý£áÈÌÀù¹)
  • disaccharidase deficiency
    ÀÌ´ç·ùºÐÇØÈ¿¼Ò°áÇÌÁõ
  • disaccharide deficiency
    ÀÌź´ç°áÇÌ
  • dissacharidase deficiency syndrome
    ÀÌ´ç·ùºÐÇØÈ¿¼Ò °áÇÌÁõÈıº(¡­ÌÀù¹ñøý¦ÏØ ).
  • electrolyte deficiency syndrome
    ÀüÇØÁú °áÇÌÁõÈıº(ï³ú°òõÌÀù¹ñøý¦ÏØ).
  • enzyme deficiency
    È¿¼Ò°áÇÌ(Áõ)
  • erythrocyte enzyme deficiency
    ÀûÇ÷±¸È¿¼Ò°áÇÌÁõ
  • erythropoietin deficiency anemia
    ¿¡¸®Æ®·ÎÆ÷¿¡Æ¾ °áÇ̼º ºóÇ÷, ÀûÇ÷
  • factor deficiency
    Á¦ÀÎÀÚ°áÇÌÁõ(ð¯ì×í­ÌÀù¹ñø).
  • factor ix deficiency
    Á¦9ÀÎÀÚ °áÇÌ(Áõ)
  • factor viii deficiency
    Á¦8ÀÎÀÚ °áÇÌ(Áõ)
  • factor viii-vwf complex deficiency
    Á¦8-vWF º¹ÇÕ °áÇÇ
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NVD nausea, vomiting, and diarrhea; neck vein distention; neovascularization of the disk; neurovesicle d...
SD Sandhoff disease; senile dementia; septal defect; serologically defined; serologically detectable; s...
SVD single vessel disease; singular value decomposition; small vessel disease; spontaneous vaginal deliv...
WD wallerian degeneration; well developed; well differentiated; wet dressing; Whitney Damon [dextrose];...
NS   1) Nephrotic Syndrome
    1. Proteinuria
   &nb...
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IgA-D IgA deficiency
ISD Intrinsic sphincter deficiency
IDD Iodine Deficiency Disorders
ID Iodine deficiency
IDA Iron Deficiency Anemia
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  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • combined system disease
    º¹ÇÕ °èÅë Áúȯ
  • combined valvular disease
    º¹ÇÕ ÆÇ¸· Áúȯ
  • connective tissue disease
    °áÇÕÁ¶Á÷ º´, °áÇÕÁ¶Á÷ Áúȯ
  • consumption disease
    ¼Ò¸ð¼º Áúȯ
    ü·ÂÀÇ ¼Ò¸ð. Àü¿¡´Â Æó °áÇÙ¿¡ ´ëÇÏ¿© »ç¿ëµÇ¾ú´Ù.
  • Creutzfeldt-Jakob disease
    ¾ß°ö º´
    ÁßÃ߽Űæ°è¸¦ ħ¹üÇÏ´Â ¹ÙÀÌ·¯½º¼º °¨¿° Áúȯ. Ä¡¸Å°¡ ¿À°Ô µÇ°í °£´ë¼º °æ·ÃÀ» º¸ÀÌ´Ù°¡ »ç¸ÁÇÏ°Ô µÇ´Â °£¿°¼º ÁúȯÀÌ´Ù. Àü¼¼°èÀûÀ¸·Î ºÐÆ÷µÇ¾î ÀÖÀ¸¸ç, Å©·ÎÀÌÃ÷ÆçÆ®-¾ß°ö º´À̶ó°íµµ ÇÑ´Ù. Àü¿° °æ·Î´Â È®½ÇÇÏ°Ô ¾Ë·ÁÁ® ÀÖÁö ¾ÊÀ¸³ª, 1996³â ¿µ±¹¿¡¼­ ¹ßº´ÇÑ ±¤¿ìº´
  • Crohn's disease
    Crohn Áúȯ, Å©·Ð¾¾ º´, Å©·Ð º´
    Å©·ÐÀÌ 1932³â óÀ½À¸·Î ȸÀå ¸»´ÜÀÇ Àå¿°À» ±¹ÇÑÀû ȸÀå¿°À¸·Î ±âÀçÇÑ °Í. ȸÀå ¸»´Ü¿°. ¼ÒÀå, ´ëÀå¿¡¼­µµ º¼ ¼ö ÀÖÀ¸¸ç ȸÀå ¸»´ÜºÎÀÇ °ÅÀÇ 30cm¿¡ ÀÚÁÖ ¹ß»ýÇϰí Á¡¸·¿¡¼­ Á¡¸· ÇÏÃþ¿¡ ¹ÌÄ¡´Â ¿°Áõ¼º º¯È­·Î À°¾Æ °Å´ë¼¼Æ÷¸¦ º¼ ¼ö ÀÖ´Ù. ¿øÀÎÀº Àå³» ¼¼±Õ, ¾Ë·¯Áö µîÀÇ ¿¬°üµÈ °ÍÀ¸·Î º¸ÀδÙ.
  • cyanotic heart disease
    û»ö¼º ½ÉÀå Áúȯ
  • cytomegalic inclusion disease
    ¼¼Æ÷ °Å´ë¼º ºÀÀÔü º´, °Å´ë ¼¼Æ÷ ºÀÀÔü Áúȯ
  • cytomegaloviral disease
    °Å´ë ¼¼Æ÷ ¹ÙÀÌ·¯½º Áúȯ
  • Darier's disease
    ´ë¸®¾î º´
    µ¿ÀǾî=
  • degenerative brain disease
    ÅðÇ༺ ³ú Áúȯ
  • degenerative disease
    ÅðÇ༺ Áúȯ
  • degenerative joint disease
    ÅðÇ༺ °üÀý Áúȯ
    °üÀý ±¸Á¶¹°¿¡ ÀûÀÀ ÇѰ踦 ³Ñ¾î¼­´Â ÈûÀÌ °è¼Ó °¡ÇØÁö¸é °üÀý¸é, Ȱ¸·, °üÀý³¶¿¡ ¿°Áõ¼º º´º¯ÀÌ »ý±â´Â °æ¿ì.
  • demyelination disease
    Å»¼öÃÊ Áúȯ
    ½Å°æ¿¡ ¼öÃʰ¡ ¾ø¾î¼­ µµ¾à Àüµµ°¡ ÀϾÁö ¾Ê¾Æ ¾ß±âµÇ´Â Áúȯµé.
  • dercums disease
    ´õÄÄ º´
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 10
deficiency dermatitis and diarrhoea, zinc A genetic disease called acrodermatitis enteropathica is characterised by the simultaneous occurrence of skin inflammation (dermatitis) and diarrhoea. The skin on the cheeks, elbows and knees and tissue about the mouth and anus are inflammed. There is also balding of the scalp, eyebrows and lashes, delayed wound healing and recurrent bacterial and fungal infections due to immune deficiency. The key laboratory finding is an abnormally low blood zinc level reflecting impaired zinc uptake. Oral treatment with zinc is curative.
(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)
deficiency, glucocerebrosidase Causes Gaucher's disease (type 1), a progressive genetic disease, due to an enzyme defect. The enzyme, glucocerebrosidase, is needed to break down the chemical glucocerebroside. The enzyme defect in persons with Gaucher's disease (GD) leads to the accumulation of glucocerebroside in the spleen, liver, and lymph nodes. The most common early sign is enlargement of the spleen (located in the upper left abdomen). Other signs include low red blood cell counts (anaemia), a decrease in blood clotting cells (platelets), increased pigmentation of the skin, and a yellow fatty spot on the white of the eye (a pinguecula). Severe bone involvement can lead to pain and collapse of the bone of the hips, shoulders, and spine. The GD gene is on chromosome 1. The disease is a recessive trait. Both parents carry a GD gene and transmit it for their child with the disease. The parents' risk of a child with the disease is 1 in 4 with each pregnancy. This type of Gaucher's disease (noncerebral juvenile Gaucher's disease) is most common in Ashkenazi Jews (of European origin) and is the most common genetic disease among Jews in the United States.
(12 Dec 1998)
deficiency, glucose-6-phosphate dehydrogenase Deficiency of G6PD is the commonest disease-causing enzyme defect in humans affecting an estimated 400 million people. The G6PD gene is on the X chromosome. Males with the enzyme deficiency develop anaemia due to breakup of their red blood cells when they are exposed to oxidant drugs such as the antimalarial primaquine, the sulfonamide antibiotics or sulfones, naphthalene moth balls, or fava beans.
(12 Dec 1998)
deficiency, iron Deficiency of iron results in anaemia because iron is necessary to make haemoglobin, the key molecule in red blood cells responsible for the transport of oxygen. In iron deficiency anaemia, the red cells are unusally small (microcytic) and pale (hypochromic). Characteristic features of iron deficiency anaemia in children include failure to thrive (grow) and increased infections. The treatment of iron deficiency anaemia , whether it be in children or adults, is with iron and iron-containing foods. Food sources of iron include meat, poultry, eggs, vegetables and cereals (especially those fortified with iron). According to the National Academy of Sciences, the Recommended Dietary Allowances of iron are 15 milligrams per day for women and 10 milligrams per day for men.
(12 Dec 1998)
deficiency, lactase Lack of the enzyme lactase resulting in failure to digest lactose in milk (lactose intolerance).
(12 Dec 1998)
deficiency, magnesium Can occur due to inadequate intake or impaired intestinal absorption of magnesium. Low magnesium (hypomagnesaemia) is often associated with low calcium (hypocalcaemia) and potassium (hypokalaemia) levels. Deficiency of magnesium causes increased irritability of the nervous system with tetany (spasms of the hands and feet, muscular twitching and cramps, spasm of the larynx, etc.). According to the National Academy of Sciences, the Recommended Dietary Allowances of magnesium are 420milligrams per day for men and 320 milligrams per day for women. The upperlimit of magnesium as supplements is 350 milligrams daily, in addition to the magnesium from food and water.
(12 Dec 1998)
deficiency mutant Mutant with a nutritional requirement not present in the wild type organism.
Synonym: defective organism, deficiency mutant.
(05 Mar 2000)
deficiency, protein c Protein C is a protein in plasma that enters into the cascade of biochemical events leading to the formation of a clot. Deficiency of protein C results in thrombotic (clotting) disease.
(12 Dec 1998)
deficiency, selenium Deficiency of the essential mineral selenium causes Keshan disease, a fatal form of cardiomyopathy (disease of the heart muscle) first observed in Keshan province in China and since found elsewhere. According to the National Academy of Sciences, the Recommended Dietary Allowances of selenium are 70 milligrams per day for men and 55 milligrams per day for women. Food sources of selenium include seafoods, some meats such as kidney and liver, and some grains and seeds.
(12 Dec 1998)
deficiency symptom Manifestation of a lack, in varying degrees, of some substance (e.g., hormone, enzyme, vitamin) necessary for normal structure and/or function of an organism.
(05 Mar 2000)
deficiency, zinc Deficiency of zinc is associated with short stature, anaemia, increased pigmentation of skin (hyperpigmentation), enlarged liver and spleen (hepatosplenomegaly), impaired gonadal function (hypogonadism), impaired wound healing, and immune deficiency. (For a genetic disorder that impairs zinc uptake, please see Acrodermatitis enteropathica). According to the National Academy of Sciences, the Recommended Dietary Allowances of zinc are 12 milligrams per day for women and 10 milligrams per day for men. Food sources of zinc include meat including liver, eggs, seafood, nuts and cereal.
(12 Dec 1998)
disaccharidase deficiency A digestive disorder caused by the body being unable to produce enough disaccharidase, an enzyme responsible for breaking down carbohydrates in the small intestine. This may cause symptoms such as intestinal gas and diarrhoea.
(09 Oct 1997)
IgA deficiency A dysgammaglobulinaemia characterised by a deficiency of IgA.
(12 Dec 1998)
IgG deficiency A dysgammaglobulinaemia characterised by a deficiency of IgG.
(12 Dec 1998)
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