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  • ¿µ¹®
    ÇѱÛ
  • molecular disease
    ºÐÀÚº´
  • Monge disease
    ¸ùÇ캴
  • motor neuron disease
    ¿îµ¿½Å°æ¼¼Æ÷º´, ¿îµ¿½Å°æ¿øº´
  • mountain disease
    °í»êº´
  • moyamoya disease
    ¸ð¾ß¸ð¾ßº´
  • muscle disease
    ±ÙÀ°º´
  • mycobacterial disease
    Ç×»ê±Õº´, ¹ÌÄÚ¹ÚÅ׸®¾Æº´
  • mycoplasma disease
    ¹ÌÄÚÇö󽺸¶º´
  • maple syrup urine disease
    ´Üdz½Ã·´´¢º´
  • marble bone disease
    ´ë¸®¼®º´, °ñÈ­¼®º´
  • Marburg disease
    ¸¶¸£ºÎ¸£Å©º´
  • Marburg virus disease
    ¸¶¸£ºÎ¸£Å©¹ÙÀÌ·¯½ºº´
  • Marchiafava-Bignami disease
    ¸¶¸£Å°¾ÆÆÄ¹Ù-ºñ³Ä¹Ìº´
  • mast cell disease
    ºñ¸¸¼¼Æ÷º´
  • McArdle¡¯s disease
    ¸Æ¾Æµéº´
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  • ¿µ¹®
    ÇѱÛ
  • neuronal storage disease
    ½Å°æ¼¼Æ÷ÀúÀ庴
  • neuropathic joint disease
    ½Å°æº´Áõ°üÀýº´
  • notifiable disease
    ½Å°í´ë»óÁúº´
  • nutritional disease
    ¿µ¾çº´
  • nutritional deficiency disease
    ¿µ¾ç°áÇ̺´
  • obliterative arterial disease
    Æó»öµ¿¸Æº´
  • obstructive pulmonary disease
    Æó¼âÆóº´
  • occlusive cerebrovascular disease
    Æó¼â³úÇ÷°üÁúȯ
  • occupational disease
    Á÷¾÷º´
  • occupational dental disease
    Á÷¾÷Ä¡°úº´
  • oculoglandular disease
    ´«»ùº´
  • oral disease
    ÀÔº´, ±¸°­Áúȯ
  • organic disease
    ±âÁúº´
  • pandemic disease
    ¹üÀ¯Çິ
  • panzootic disease
    µ¿¹°¹üÀ¯Çິ
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  • ¿µ¹®
    ÇѱÛ
  • allergic respiratory disease
    ¾Ë·¹¸£±â¼º È£Èí±âº´
  • allergic skin disease
    ¾Ë·¹¸£±â(¼º)ÇǺΠÁúȯ
  • allergic skin disease
    ¾Ë·¹¸£±â[¼º] ÇǺκ´
  • alpha chain disease
    ¾ËÆÄ¼âº´(¡­áðÜ»).
  • alpha chain disease
    ¾ËÆÄ¼âÁúȯ
  • alpha-chain disease
    ¾ËÆÄ¼â Áúȯ(¡­áð òðü´)
  • alports syndrome(disease)
    ¾ËÆ÷Æ® ÁõÈıº(º´)(¡­ñøý¦ÏØ)
  • aluminium dust disease
    ¾Ë·ç¹Ì´½°¡·çº´(ÊÙËÓ).
  • alzheimers disease
    ¾ËÂêÇÏÀ̸Ӻ´(¡­Ü»)
  • amaurotic familial idiocy =Tay-Sachs disease
    °¡Á·¼ºÈæ¾Ï½Ã¹éÄ¡(Ê«ðéàõýÙÒ®î¡ÛÜöÁ).
  • amaurotic familial idiocy =Tay-Sachs disease
    °¡Á·¼º Èæ³»Àå ¹éÄ¡(Ê«ðéàõýÙÒ®î¡ÛÜöÁ).
  • amyloid disease
    ¾Æ¹Ð·ÎÀ̵庴(¡­Ü»).
  • andersen disease
    ¾Ø´õ½¼º´<--Áúȯ>
  • angiospasmodic disease
    Ç÷°ü¿¬Ã༺ Áúȯ.
  • aortic valvular disease
    ´ëµ¿¸ÆÆÇÁúȯ(¡­òðü´).
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  • ¿µ¹®
    ÇѱÛ
  • creutzfeldt-jakob disease
    Å©·ÎÀÌÃ÷ÆçÆ®¾ßÄߺ´(¡­Ü»)
  • crohns disease
    Å©·Ð º´(¡­Ü»)
  • cystic disease of liver
    °£³¶¼ºÁúȯ(ÊÜÒ¥àõ òðü´).
  • cystic disease of liver
    ³¶¼º°£Áúȯ(³¶¼º°£Áúȯ).
  • cystic disease of lung
    È£Èí ³¶¼ºÆóÁúȯ(Ò¥àõøËòðü´).
  • cystic kidney disease
    ³¶¼º½ÅÁúȯ(Ò¥àõãìòðü´).
  • cystine disease
    ½Ã½ºÆ¾º´(¡­Ü»).
  • cystine storage disease
    ½Ã½ºÆ¾(ÃàÀû)º´ (¡­õëîÝÜ»).
  • cytomegalic inclusion disease
    ¼¼Æ÷ °Å´ë ºÀÀÔü º´
  • cytomegalic inclusion disease
    ¼¼Æ÷°Å´ëÈ­ ºÀÀÔüº´
  • cytomegalic inclusion disease =CID
    ¼¼Æ÷°Å´ë¼º ºÀÀÔüº´(¡­ËÝÓÞàõÜæìýô÷ Ü»), °Å´ë¼¼Æ÷ ºÀÀÔüÁúȯ(ËÝÓÞá¬øàÜæìýô÷òðü´).
  • cytomegalic inclusion disease =CID
    ¼¼Æ÷°Å´ë¼º ºÀÀÔüº´(¡­ËÝÓÞàõÜæìýô÷ Ü»), °Å´ë¼¼Æ÷ ºÀÀÔüÁúȯ(ËÝÓÞá¬øàÜæìýô÷òðü´).
  • cytomegalic inclusion disease =CID
    °Å´ë¼¼Æ÷ºÀÀÔüÁúȯ(ËÝÓÞá¬øàÜæìýô÷òðü´).
  • cytomegalic inclusion disease =cid
    °Å´ë¼¼Æ÷¼º ºÀÀÔüº´(¡­ËÝÓÞàõÜæìýô÷ Ü»), °Å´ë¼¼Æ÷ ºÀÀÔüÁúȯ(¡­òðü´)
  • degenerative brain disease
    ÅðÇ༺ ³úÁúȯ.
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SLHR sex-linked hypophosphatemic rickets
SPGX spastic paraplegia, X-linked
XBSN X-linked bulbospinal neuropathy
Xfb cross-linked Gibrin
XL excess lactate; X-linked [inheritance]; xylose-lysine [agar base]
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AOD Arterial Occlusive Disease
ASCVD Atherosclerotic cardiovascular disease
AD Aujeszky disease
ADV Aujeszky Disease Virus
AITD Autoimmune Thyroid Disease
°æºÏ´ë Ä¡°ú´ëÇÐ ±¸°­³»°ú ±³½Ç »çÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 15
  • ¿µ¹®
    ÇѱÛ
    ¼³¸í
  • polycystic disease
    ´Ù³¶¼º Áúȯ
  • polycystic kidney disease
    ´Ù³¶ ½Å Áúȯ
  • polycystic ovarian disease
    ´Ù³¶ ³­¼Ò Áúȯ
  • polyendocrine autoimmune disease
    ´Ù³»ºÐºñ¼± ÀÚ°¡ ¸é¿ª Áúȯ
    µ¿ÀǾî=autoimmune
  • Pospischill-Feyrter disease
    Pospischill-Feyrter º´
  • Preiser's disease
    Preiser º´
  • prenatal disease
    Ãâ»ý Àü Áúȯ
    žƱ⠶§ Áúº´À» °¡Áö´Â »óÅÂ.
  • previous dental disease
    ÀÌÀüÀÇ Ä¡°ú Áúȯ
  • professional disease
    Àü¹®Á÷º´, Á÷¾÷º´
  • progress of disease
    º´ÀÇ °æ°ú, º´ÀÇ ÁøÇà
    Áúº´ÀÌ ¾ÕÀ¸·Î ÁøÇàÇÏ¿© ¿øÇÏÁö ¾Ê´Â °á°ú¸¦ ÃëÇÏ´Â °Í
  • psychological disease
    ½É¸® Áúȯ
  • quarantinable disease
    °Ë¿ª Áúȯ
  • Raynaud's disease
    ·¹ÀÌ³ë º´
    ¿ø¹ß¼º ¶Ç´Â Ư¹ß¼º Ç÷°ü Àå¾Ö·Î ¾çÃøÀÇ ·¹À̳ë Çö»óÀÇ ¹ßÀÛÀÌ Æ¯Â¡. ³²¼ºº¸´Ù´Â ¿©¼ºÀÌ ¹ßº´Çϱ⠽±´Ù.
  • reactive disease
    ¹ÝÀÀ¼º Áúȯ
  • Recklinghausen's disease
    Recklinghausen º´
    ´Ù¹ß, ´ÙÇü¼º ½Å°æ ¼¶À¯Á¾À̸ç, ±× ¹Û¿¡µµ »À, ÁßÃß ½Å°æ, ÀÚÀ² ½Å°æ µî¿¡µµ Á¾·ù¸¦ Çü¼ºÇÏ´Â ÇϳªÀÇ µ¶¸³ ÁúȯÀÌ´Ù. º´¸íÀº µ¶ÀÏÀÇ º´¸®ÇÐÀÚ F.D.von ·¹Å¬¸µÇÏ¿ìÁ¨
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Gaucher's disease <disease> A chronic congenital disease of lipid metabolism caused by a deficiency of the beta-glucocerebrosidase enzyme. The defect is most common in Ashkenazi Jews. Clinical features are hepatosplenomegaly (enlargement of liver and spleen) and in severe early onset forms of the disease, with neurological dysfunction.
Inheritance: autosomal recessive.
(27 Sep 1997)
gaucher's disease, type 1 A progressive genetic disease caused by a defect in an enzyme. The enzyme, called 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)
Ranikhet disease An influenza-like viral disease of birds, including domestic fowl, characterised by respiratory and gastrointestinal or pneumonic and encephalitic symptoms. First seen near newcastle, england, the infection is also transmissible to humans by contact with infected birds.
(12 Dec 1998)
manic-depressive disease See manic-depression.
(12 Dec 1998)
rat-bite disease A syndrome characterised by recurring fever, rash, and arthralgias occurring days to weeks after a rat bite. The causative agents are either streptobacillus moniliformis or spirillum minus.
(12 Dec 1998)
generalised small bowel disease <radiology> Hypoproteinaemia, sprue, Whipple
(12 Dec 1998)
Raussly disease A rare autosomal dominant neurological disorder with many of the clinical features of hereditary hypertrophic sensorimotor polyneuropathy combined with an essential tremor.
Synonym: hereditary areflexic dystasia.
(05 Mar 2000)
venereal disease <microbiology> A disease contracted through sexual intercourse.
Examples include syphilis, gonorrhoea, chlamydia and lymphogranuloma venereum.
Synonym: sexually transmitted disease.
(12 Jan 1998)
Venereal Disease Research Laboratory <microbiology> A blood test used to diagnose syphilis.
Read as nonreactive or negative if you do not have syphilis. The Venereal Disease Research Laboratory can also be positive is cases of leprosy, malaria, mononucleosis, lupus, hepatitis A and pregnancy.
Positive Venereal Disease Research Laboratory tests are usually followed up by a more specific test (FTA antibodies).
(12 Jan 1998)
Manson's disease Schistosomiasis caused by schistosoma mansoni. It is endemic in africa, the middle east, south america, and the caribbean and affects mainly the bowel, spleen, and liver.
(12 Dec 1998)
Rayer's disease Xanthomatosis with hypercholesterolaemia, resulting from biliary cirrhosis.
Synonym: Rayer's disease.
(05 Mar 2000)
Raynaud's disease <disease> Paroxysmal spasm of the digital arteries causing pallor (blanching) of the fingers and toes.
Maurice Raynaud, French physician (1834-81).
(27 Sep 1997)
veno-occlusive disease <haematology, oncology> A disease that sometimes occurs following high-dose chemotherapy or radiation, in which the blood vessels that carry blood through the liver become swollen and clogged.
Acronym: VOD
(12 Jan 1998)
veno-occlusive disease of the liver Obliterating endophlebitis of small hepatic vein radicles, described in Jamaican children, associated with ingestion of toxic plant substances in bush tea; causes ascites, which may progress to cirrhosis.
(05 Mar 2000)
maple bark disease <radiology> Type of extrinsic allergic alveolitis, source: moldy maple bark in saw mills, organism: Cryptostroma corticale
(12 Dec 1998)
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