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"fat deficiency disease"¿¡ ´ëÇÑ °Ë»ö °á°úÀÔ´Ï´Ù. °Ë»ö °á°ú º¸´Â µµÁß¿¡ Tab ۸¦ ´©¸£½Ã¸é °Ë»ö âÀÌ ¼±Åõ˴ϴÙ.
À̰ÍÀ» ¿øÇϼ̽À´Ï±î?
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  • ¿µ¹®
    ÇѱÛ
  • Fordyce¡¯s disease
    Æ÷´ÙÀ̽ºº´
  • functional cardiovascular disease
    ±â´É¼º½É(Àå)Ç÷°üº´
  • fungal disease
    Áø±ÕÁúȯ, °õÆÎÀ̺´
  • fusospirochetal disease
    ¹æÃß±Õ½ºÇÇ·ÎÇ쟺´
  • gastroesophageal reflux disease
    À§½Äµµ¿ª·ùº´
  • genetic disease
    À¯Àüº´
  • gestational trophoblastic disease
    Àӽſµ¾ç¸·º´
  • glomerular disease
    Å丮º´, »ç±¸Ã¼Áúȯ
  • gamma chain disease
    °¨¸¶»ç½½º´
  • glycogen storage disease
    ±Û¸®ÄÚ°ÕÃàÀûº´, ´ç¿øÃàÀûº´
  • graft-versus-host disease
    ÀÌ½ÄÆí´ë¼÷ÁÖº´
  • granulomatous disease
    À°¾ÆÁ¾º´
  • Greenfield¡¯s disease
    ±×¸°Çʵ庴
  • Hartnup¡¯s disease
    ÇÏÆ®³Òº´
  • Hashimoto¡¯s disease
    ÇϽøðÅ亴
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  • ¿µ¹®
    ÇѱÛ
  • epidermal-epithelial viral disease
    Ç¥ÇÇ»óÇǹÙÀÌ·¯½ºº´
  • exotic disease
    ¿Ü·¡º´
  • extraarticular rheumatic disease
    °üÀý¿Ü·ù¸¶Æ¼½ºº´
  • extrapyramidal disease
    Ãßü¿Ü·Îº´
  • febrile disease
    ¿­º´
  • fibrocystic disease
    ¼¶À¯³¶º´
  • fibromuscular disease
    ¼¶À¯±ÙÀ°º´
  • fifth disease
    (¢¡erythema infectiosum) °¨¿°È«¹Ý
  • fishskin disease
    (¢¡ichthyosis) ºñ´ÃÁõ
  • fluke disease
    ÈíÃæº´
  • foot process disease
    ¹ßµ¹±âº´
  • foot-and-mouth disease
    ÀԹ߱Áº´, ±¸Á¦¿ª
  • functional cardiovascular disease
    ±â´É½ÉÀåÇ÷°üº´
  • fungal disease
    Áø±Õº´, Áø±ÕÁúȯ, °õÆÎÀ̺´
  • gamma chain disease
    °¨¸¶°í¸®º´
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  • ¿µ¹®
    ÇѱÛ
  • Grovers disease => transient acantholytic dermatosis
    Àϰú¼º ±Ø¼¼Æ÷ÇØ¸® ÇǺÎÁõ
  • Gunthers disease => congenital erythropoietic porphyria
    ¼±Ãµ¼º ÀûÇ÷±¸ Á¶Ç÷¼º Æ÷¸£ÇǸ° Áõ
  • H chain disease
    H-¼âº´, Á߼⺴.
  • H chain disease
    Á߼⺴
  • Hailey-Hailey disease = familial benign chronic pemphigus
    ÇìÀϸ®-ÇìÀϸ®º´
  • Hand Schueller Christian disease
    ÇÚµå-½¯·¯-Å©¸®½ºÂùº´.
  • Hansen disease
    ÇѼ¾º´ ³ªº´ .
  • Hansen disease = leprosy
    ÇѼ¾º´, ³ªº´
  • Hansens disease
    ÇѼ¾º´, ³ª, ³ªº´
  • Harada disease
    Ç϶ó´Ùº´
  • Haradas disease
    Ç϶ó´Ùº´.
  • Hartnup disease
    ÇÏ¾ÆÆ®´¯º´.
  • Hartnups disease
    ÇÏ¾ÆÆ®´¯º´
  • Hashimoto s disease =H. thyroiditis
    ÇϽà ¸ðÅ亴.
  • Hashimotos disease =H. thyroiditis
    ÇϽøðÅ亴.
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    ÇѱÛ
  • familial apolipoprotein CII deficiency
    °¡Á·¼º ¾ÆÆ÷Áö¹æ´Ü¹é CII °áÇÌÁõ
  • folate deficiency
    ¿±»ê°áÇÌ(ç¨ß«ÌÀù¹)
  • folic acid deficiency
    ¿±»ê°áÇÌÁõ.
  • folic acid deficiency
    ¿±»ê°áÇÌ(ç¨ß«ÌÀù¹)
  • folic acid deficiency
    ¿±»ê°áÇÌÁõ
  • folic acid deficiency anemia
    ¿±»ê°áÇ̼º ºóÇ÷(ç¨ß«ÌÀù¹àõÞ¸úì).
  • fructokinase deficiency
    ÇÁ¶ôÅäŰ³ªÁ¦°áÇÌ
  • functional deficiency
    ±â´É°áÇÌ
  • g6pd deficiency
    G6PD(Æ÷µµ´ç-6-Àλ꿰 Å»¼ö¼ÒÈ¿¼Ò) °áÇÌÁõ
  • galactosidase, alpha-galactosidase a, deficiency
    #NAME?
  • gistdase deficiency
  • glucocerebrosidase deficiency
    ±Û·çÄÚ¼¼·¹ºê·Î½Ãµ¥À̽º °áÇÌÁõ
  • glucose 6 phosphatase deficiency hepa
    ±Û·çÄÚ¿À½º-6 -ÀÎ»ê °áÇ̰£½ÅÇü´ç
  • glucose-6-phosphate dehydrogenase deficiency
    ±Û·çÄÚ½º-6-ÀλêµðÇÏÀÌ µå·ÎÀú³×À̽º °áÇÌ(Áõ)
  • glutathione reductase deficiency
    ±Û·çŸƼ¿Â ȯ¿øÈ¿¼Ò °áÇÌÁõ.
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CR calculation rate; calculus removed; calorie-restricted; cardiac rehabilitation; cardiac resuscitatio...
FAT family attitudes test; fluorescent antibody technique; fluorescent antibody test
FES family environment scale; fat embolism syndrome; flame emission spectroscopy; forced expiratory spir...
FF degree of fineness of abrasive particles; fat-free; father factor; fecal frequency; fertility factor...
FFDW fat-free dry weight
KMLE ÀÚµ¿ÃßÃâ ÀÇÇоà¾î »çÀü À¯»ç °Ë»ö °á°ú : 5 ÆäÀÌÁö: 11
ID Iron deficiency
IGHD Isolated GH deficiency
IGHD Isolated Growth Hormone Deficiency
LAD Leucocyte adhesion deficiency
LPD Luteal phase deficiency
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  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • devics disease
    µ¥ºò º´
    µ¿ÀǾî=o
  • digestive tract disease
    ¼ÒÈ­±â °èÅë Áúȯ
  • disease
    º´, Áúº´, Áúȯ
    ÀÎÁö °¡´ÉÇÑ ÀÏ·ÃÀÇ Â¡ÈÄ¿Í Áõ»ó, ½Åü ¼Ò°ßÀÌ Æ¯Â¡ÀÎ Áúº´
  • disease entity
    Áúº´ ´ÜÀ§
  • disease of the esophagus
    ½Äµµ Áúȯ
  • disease of the lymphreticular system
    ¸²ÇÁ ¼¼¸Á³»ÇǰèÀÇ Áúȯ
  • disease of the pancreas
    ÃéÀå Áúȯ
  • double vessel disease
    ÀÌÁß °ü»ó µ¿¸Æ Áúȯ
  • Ebstein anomaly disease
    ¿¦½ºÅ¸ÀÎ º´
    ¿ì½É½Ç°ú ¿ì½É¹æ »çÀÌ¿¡ ÀÖ´Â »ï÷ÆÇ
  • epizootic hemorrhagic disease
    °¡Ãà À¯Ç༺ ÃâÇ÷¼º Áúȯ
  • F1 hybrid disease
    F1 ÇÏÀ̺긮µå Áúȯ
    ÇÑÂÊ ¾î¹öÀÌÀÇ ¸é¿ª ´ã´ç ¼¼Æ÷¸¦ F
  • Fabry Anderson disease
    ÆÐºê¸® ¾Ø´õ½¼ Áúȯ
  • febrile disease
    ¿­¼º Áúȯ
  • fifth disease
    Á¦ 5º´
  • flat Bowen's disease
    ÆíÆò Bowen Áúȯ
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 11
immune deficiency Impaired ability of the bodys defence mechanisms to combat infections by bacteria, viruses and fungi.
(13 Nov 1997)
immune deficiency diseases Those diseases in which immune reactions are suppressed or reduced. Reasons may include congenital absence of B and/or T lymphocytes or viral killing of helper lymphocytes (see HIV).
(18 Nov 1997)
immunity deficiency Inabillity to mount a normal immune response. Immunodeficiency can be due to a genetic disease or acquired as in aids due to HIV.
(12 Dec 1998)
immunoglobulin G subclass deficiency A rare inherited disorder in which there are reduced levels of one or more IgG subclasses resulting from defective heavy chain genes or an abnormality in the regulation of immunoglobulin isotype switching.
(05 Mar 2000)
immunological deficiency Inabillity to mount a normal immune response. Immunodeficiency can be due to a genetic disease or acquired as in aids due to HIV.
(12 Dec 1998)
immunologic deficiency syndromes Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral.
(12 Dec 1998)
iodine deficiency Iodine is a natural requirement of our diets. Iodine deficiency can lead to inadequate production of thyroid hormone from the thyroid gland (hypothyroidism). For example, in some parts of zaire, ecuador, india, and chile, remote, mountainous areas, such as in the alps (in the past), andes and the himalayas have a particular predisposition to severe iodine deficiency, goiter, and hypothyroidism. Since the addition of iodine to table salt, iodine deficiency is rarely seen in the united states.
(12 Dec 1998)
iron deficiency 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)
iron deficiency anaemia Hypochromic microcytic anaemia characterised by low serum iron, increased serum iron-binding capacity, decreased serum ferritin, and decreased marrow iron stores.
Synonym: hypoferric anaemia.
(05 Mar 2000)
taste deficiency Reduced or absent ability to detect a bitter taste in a group of compounds of which phenylthiocarbamide is the prototype, due to the homozygous state of a common allele.
See: phenylthiourea.
(05 Mar 2000)
thiamin deficiency An endemic form of polyneuritis (nerve inflammation), due to an unbalanced diet, with a deficiency of vitamin B1(thiamin). Common in those who chronically abuse alcohol.
Synonym: beriberi.
(27 Sep 1997)
thiamine deficiency A nutritional condition produced by a deficiency of thiamine in the diet, characterised by anorexia, irritability, and weight loss. Later, patients experience weakness, peripheral neuropathy, headache, and tachycardia. In addition to being caused by a poor diet, thiamine deficiency in the united states most commonly occurs as a result of alcoholism, since ethanol interferes with thiamine absorption. In countries relying on polished rice as a dietary staple, beriberi prevalence is very high.
(12 Dec 1998)
transferase deficiency galactosaemia An autosomal recessive disorder in which there is a deficiency of galactose-1-phosphate uridylyltransferase (see main entry for galactosaemia).
(05 Mar 2000)
epimerase deficiency galactosaemia An inborn error in metabolism in which there is a deficiency of uridine diphosphate galactose 4-epimerase; galactose 1-phosphate accumulates.
(05 Mar 2000)
extrinsic factor deficiency <disease> An inherited disorder that causes abnormal blood clotting due to the congenital absence of one of the 20 different plasma proteins involved in the coagulation process.
Symptoms include bleeding of the gums, nosebleeds, easy bruising, bleeding in muscles or joints and excessive menstrual bleeding.
Treatment includes the administration of plasma concentrates of factor VII (extrinsic factor).
(27 Sep 1997)
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