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  • ÄÚµå
    ¿µ¹®
    ÇѱÛ
  • K51.5
    Mucosal proctocolitis
    Á¡¸·¼º Á÷Àå°áÀå¿°
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  • ¿µ¹®
    ÇѱÛ
  • mucoid
    1. Á¡¾×¼º, ¹ÂÄÚÀ̵å 2. Á¡¾×¸ð¾ç-
  • mucoid colony
    Á¡¾×Áý¶ô
  • mucolipidosis
    Á¡¾×ÁöÁúÁõ
  • mucolytic
    1. Á¡¾×¿ëÇØ- 2. Á¡¾×¿ëÇØÁ¦
  • mucolytic agent
    Á¡¾×¿ëÇØÁ¦
  • mucoperiosteal flap
    Á¡¸·»À¸·ÇÇÆÇ, Á¡¸·°ñ¸·ÇÇÆÇ
  • mucoperiosteum
    Á¡¸·»À¸·, Á¡¸·°ñ¸·
  • mucopolysaccharide
    Á¡¾×´Ù´ç·ù, ¹ÂÄÚ´Ù´ç·ù
  • mucopolysaccharidosis
    Á¡¾×´Ù´ç·ùÁõ, ¹ÂÄÚ´Ù´ç·ùÁõ
  • mucoprotein
    Á¡¾×´Ü¹éÁú, ¹ÂÄڴܹéÁú
  • mucopurulent
    Á¡¾×°í¸§-, Á¡¾×³ó-
  • mucopus
    °í¸§¸ð¾çÁ¡¾×, Á¡¾×³ó
  • Mucor
    ÅаõÆÎÀÌ(¼Ó)
  • Mucor corymbifer
    »ñ°«ÅаõÆÎÀ̱Õ
  • Mucoraceae
    ÅаõÆÎÀÌ(°ú)
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  • ¿µ¹®
    ÇѱÛ
  • mucolipidosis
    Á¡¾×ÁöÁúÁõ
  • mucolytic
    Á¡¾×¿ëÇØÁ¦, Á¡¾×¿ëÇØ-
  • mucolytic agent
    Á¡¾×¿ëÇØÁ¦
  • mucolytic enzyme
    Á¡¾×ºÐÇØÈ¿¼Ò
  • mucoperiosteal flap
    Á¡¸·°ñ¸·ÇÇÆÇ
  • mucoperiosteum
    Á¡¸·»À¸·, Á¡¸·°ñ¸·
  • mucoperiostitis
    Á¡¸·»À¸·¿°, Á¡¸·°ñ¸·¿°
  • mucopolysaccharide
    Á¡¾×´Ù´ç·ù
  • mucopolysaccharidosis
    Á¡¾×´Ù´ç·ùÁõ
  • mucoprotein
    Á¡¾×´Ü¹éÁú
  • mucopurulent
    Á¡¾×°í¸§-
  • mucopurulent sputum
    Á¡¾×°í¸§°¡·¡, Á¡¾×³ó°¡·¡
  • Mucor
    ÅаõÆÎÀÌ
  • Mucor corymbifer
    »ñ°«ÅаõÆÎÀ̱Õ
  • Mucoraceae
    ÅаõÆÎÀÌ
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  • mucinous carcinoma
    Á¡¾×¾ÏÁ¾(¡­äßðþ)
  • mucinous carcinoma
    Á¡¾×¾ÏÁ¾(¡­äßðþ).
  • mucinous corneal degeneration
    Á¡¾×°¢¸·º¯¼º
  • mucinous eccrine carcinoma
    Á¡¾×¼º ÇѼ± ¾ÏÁ¾
  • mucinous exudate
    Á¡¾×»ó »ïÃâ¾×(¡­ßÒß¶õóäû).
  • mucinous syringometaplasia
    Á¡¾×¼º ÇѰü ÀÌÇü¼ºÁõ
  • mucinous tumor
    Á¡¾×¼º Á¾¾ç(¡­àõ ðþåË)
  • mucinuria
    Á¡¾×´¢(ïÄäûèñ).
  • muciparous gland
    Á¡¾×¼±(ïÄäûàÍ).
  • muciparous ³ª muciparus
    Á¡¾×ºÐºñ(ïÄäûÝÂù²).
  • mucoblast
    Á¡¾×¾Æ¼¼Æ÷
  • mucobromic acid
    ¹«ÄÚºê·Ò»ê(¡­ß«).
  • mucobuccal fold
    ÀºÇùÀÌÇàºÎ(ó» ì¹ú¼Ý»).
  • mucobuccal fold
    ÀºÇùÀÌÇàºÎ
  • mucocartilage
    Á¡¸·¿¬°ñ(ïÄØ¯æãÍé).
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    ¼³¸í
  • mucosal neuroma
    Á¡¸· ½Å°æÁ¾
    ÀüÇüÀûÀÎ ¼öÁú ¾ÏÁ¾°ú Å©·Ò ģȭ ¼¼Æ÷Á¾À» µ¿¹ÝÇϸ鼭 ±× À§¿¡ ÀÔ¼ú, ±¸°­, ´«, ±âµµ, ¼ÒÈ­±â°è, ¹æ±¤ µî ¿©·¯ Àå¼Ò¿¡ ½Å°æÁ¾ ¶Ç´Â ½Å°æÀý ½Å°æÁ¾À» µ¿¹ÝÇÏ´Â °ÍÀ» Ư¡À¸·Î ÇÑ´Ù.
  • mucosal pattern
    Àḷ »ó, Á¡¸·Çü
  • mucosal ridging
    Á¡¸· ¾ÐÈç, Á¡¸·ÀÇ ¾ÐÈç
  • mucosal thickening
    Á¡¸· ºñÈÄ
  • mucosal tuberculosis
    Á¡¸· °áÇÙ
  • mucosal-colored tumor
    Á¡¸·»ö Á¾¾ç
  • mucosedative
    Á¡¸· ÁøÁ¤Á¦
  • mucositis
    Á¡¸·¿°
  • mucostatic
    Á¡¸· ¾ÈÁ¤ÀÇ
  • mucosus
    Á¡¾×ÀÇ, Á¡¾×¼ºÀÇ
    µ¿ÀǾî=mucous.
  • mucosus blanket
    Á¡¾×¸·Ãþ
  • mucous
    Á¡¾×ÀÇ, Á¡¾×¼ºÀÇ
  • mucous adenocarcinoma
    Á¡¾×¼± ¾Ï
  • mucous cell
    Á¡¾× ¼¼Æ÷
  • mucous coat of mouth
    ÀÔ Á¡¸·
CancerWEB ¿µ¿µ ÀÇÇлçÀü ¸ÂÃã °Ë»ö °á°ú : 15 ÆäÀÌÁö: 3
mucinoid degeneration A term including both mucoid and colloid degeneration, the essential cellular changes in both being similar, the only difference being that, in colloid degeneration, the substance is firmer and more inspissated than in mucoid degeneration, in which it is thin and jelly-like.
(05 Mar 2000)
mucinolytic Capable of bringing about the hydrolysis of mucin, as by a mucinase.
(05 Mar 2000)
mucinoses Mucoid states characterised by the elevated deposition and accumulation of mucin (mucopolysaccharides) in dermal tissue. The fibroblasts are responsible for the production of acid mucopolysaccharides (glycosaminoglycans) in the ground substance of the connective tissue system. When fibroblasts produce abnormally large quantities of mucopolysaccharides as hyaluronic acid, chondroitin sulfate, or heparin, they accumulate in large amounts in the dermis.
(12 Dec 1998)
mucinosis A condition in which mucin is present in the skin in excessive amounts, or in abnormal distribution; classified as:
(05 Mar 2000)
mucinosis, follicular A disease of the pilosebaceous unit, presenting clinically as grouped follicular papules or plaques with associated hair loss. It is caused by mucinous infiltration of tissues, and usually involving the scalp, face, and neck. It may be primary (idiopathic) or secondary to mycosis fungoides or reticulosis.
(12 Dec 1998)
mucinous Relating to or containing mucin.
Synonym: mucoid.
(05 Mar 2000)
mucinous carcinoma <tumour> A variety of adenocarcinoma in which the neoplastic cells secrete conspicuous quantities of mucin, and, as a result, the neoplasms are likely to be glistening, sticky, and gelatinoid in consistency.
Synonym: colloid cancer, colloid carcinoma.
(05 Mar 2000)
mucinous cystic neoplasm of pancreas <radiology> = macrocystic adenoma of pancreas, cystadenoma / cystadenocarcinoma, M:F = 1:9, 40-60 years of age, malignant or pre-malignant, large mass (mean 12 cm), multilocular cysts, thick septations, tail / body in 85% (unlike adenocarcinoma and microcystic adenoma), hypo-/avascular, Differential diagnosis: panc pseudocyst, ** Cf: microcystic adenoma
(12 Dec 1998)
mucins A secretion containing mucopolysaccharides and protein that is the chief constituent of mucus.
(12 Dec 1998)
mucinuria The presence of mucin in the urine.
Origin: mucin + G. Ouron, urine
(05 Mar 2000)
muciparous <physiology> Secreting, or producing, mucus or mucin.
Origin: Mucus + L. Parere to produce.
Source: Websters Dictionary
(01 Mar 1998)
muciparous gland <anatomy> A type of merocrine gland that produces a thick (mucopolysaccharide rich) secretion as opposed to a serous gland).
(18 Nov 1997)
mucitis Inflammation of a mucous membrane.
(05 Mar 2000)
mucivore <zoology> An unsect which feeds on mucus, or the sap of plants, as certain Diptera, of the tribe Mucivora.
Origin: L. Mucus slime, mucus + vorare to devour.
Source: Websters Dictionary
(01 Mar 1998)
Muckle, T <person> 20th century Canadian paediatrician.
See: Muckle-Wells syndrome.
(05 Mar 2000)
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 5 ÆäÀÌÁö: 3
  • Mucopolysaccharidosis II - »õâ Systemic lysosomal storage disease marked by progressive physical deterioration and caused by a deficiency of L-sulfoiduronate sulfatase. This disease differs from MUCOPOLYSACCHARIDOSIS I by slower progression, lack of corneal clouding, and X-linked rather than autosomal recessive inheritance. The mild form produces near-normal intelligence and life span. The severe form usually causes death by age 15.
    Synonyms : Hunter Syndrome Gargoylism, Mucopolysaccharidosis 2, Gargoylisms, Hunter Syndrome, Hunter Syndrome, Hunter Syndrome Gargoylisms, Hunters Syndrome, IIs, Mucopolysaccharidosis, Mucopolysaccharidosis IIs, Syndrome, Hunter's
  • Mucopolysaccharidosis III - »õâ Mucopolysaccharidosis characterized by heparitin sulfate in the urine, progressive mental retardation, mild dwarfism, and other skeletal disorders. There are four clinically indistinguishable but biochemically distinct forms, each due to a deficiency of a different enzyme.
    Synonyms : MPS III A, MPS III B, MPS III C, MPS III D, Mucopolysaccharidosis 3, San Filippo's Syndrome, IIIs, Mucopolysaccharidosis, Mucopolysaccharidosis IIIs, Oligophrenia, Polydystrophic, Oligophrenias, Polydystrophic, Polydystrophic Oligophrenias, San Filippo Syndrome
  • Mucopolysaccharidosis IV - »õâ Genetic disorder of mucopolysaccharide metabolism characterized by skeletal abnormalities, joint instability, development of cervical myelopathy, and excessive urinary keratan sulfate. There are two biochemically distinct forms, each due to a deficiency of a different enzyme.
    Synonyms : Eccentroosteochondrodysplasia, MPS IV A, MPS IV B, Morquio Disease, Morquio's Syndrome, Mucopolysaccharidosis 4, Disease, Morquio, Disease, Morquio's, Eccentro Osteochondrodysplasia, Eccentro-Osteochondrodysplasias, Eccentroosteochondrodysplasias
  • Mucopolysaccharidosis VI - »õâ Mucopolysaccharidosis with excessive chondroitin sulfate B in urine, characterized by dwarfism and deafness. It is caused by a deficiency of N-acetylgalactosamine-4-sulfatase (arylsulfatase B).
    Synonyms : Mucopolysaccharidosis 6, Dwarfism, Polydystrophic, Maroteaux Lamy Syndrome, Mucopolysaccharidosis VIs, Syndrome, Maroteaux-Lamy, VIs, Mucopolysaccharidosis
  • Mucopolysaccharidosis VII - »õâ Mucopolysaccharidosis characterized by excessive dermatan and heparan sulfates in the urine and Hurler-like features. It is caused by a deficiency of beta-glucuronidase.
    Synonyms : Mucopolysaccharidosis 7, Sly Disease, Disease, Sly, Mucopolysaccharidosis VIIs, Syndrome, Sly, VIIs, Mucopolysaccharidosis
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mucopolysaccharidosis any of a group of genetic disorders involving a defect in the metabolism of mucopolysaccharides resulting in greater than normal levels of mucopolysaccharides in tissues
Ãâó: wordnet.princeton.edu/perl/webwn
mucopurulent containing or composed of mucus and pus
Ãâó: wordnet.princeton.edu/perl/webwn
Mucor any mold of the genus Mucor
Ãâó: wordnet.princeton.edu/perl/webwn
mucosa mucous membrane: mucus-secreting membrane lining all body cavities or passages that communicate with the exterior
Ãâó: wordnet.princeton.edu/perl/webwn
mucous of or secreting or covered with or resembling mucus; "mucous tissue"; "mucous glands of the intestine"
Ãâó: wordnet.princeton.edu/perl/webwn
WordNet ÀÏ¹Ý ¿µ¿µ »çÀü °Ë»ö °á°ú : 12 ÆäÀÌÁö: 3
MUC soil with mud, muck, or mire
MUC make a mess of, destroy or ruin
MUC a heap of dung or refuse
MUC a heap of dung or refuse
MUC (often followed by `of') a large number or amount or extent
MUC explore and expose misconduct and scandals concerning public figures
MUC one who spreads real or alleged scandal about another (usually for political advantage)
MUC the exposure of scandal (especially about public figures)
MUC dirty and messy
MUC (of soil) soft and watery
MUC of or relating to the mucous membranes and skin
MUC a form of leishmaniasis endemic in Mexico and Central American and South America
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