| mucolipidosis I | <biochemistry> Mucolipidosis somewhat like a mild form of Hurler's syndrome with mild dysostosis multiplex, and moderate mental retardation due to neuraminidase deficiency. Inheritance: autosomal recessive. Synonym: lipomucopolysaccharidosis. (05 Mar 2000) |
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| mucolipidosis II | <biochemistry> Mucolipidosis of early onset and with severe symptoms like those in Hurler's syndrome but with normal urinary mucopolysaccharides, vacuolated lymphocytes, and inclusion bodies in cultured fibroblasts (I-cells). The lysosomes lack hydrolases but high concentrations of lysosomal enzymes are found in the extracellular fluids such as serum, spinal fluid, and urine. It is associated with a deficiency of N-acetylglucosaminyl-1-phosphotransferase. The gene defect responsible probably prevents the addition of the lysosome recognition marker mannose 6 phosphate) to these enzymes so that they are not directed into the lysosomes but are released. Inheritance: autosomal recessive. Synonym: I-cell disease, inclusion cell disease. (12 Jul 2000) |
| mucolipidosis III | <biochemistry> Mucolipidosis with mild Hurler-like symptoms, restricted joint mobility, short stature, mild mental retardation, and dysplastic skeletal changes, especially of the hip. Aortic and mitral valve disease are often present. It is associated with a deficiency of UDP-N-acetyl glucosamine and lysosomal enzyme N-acetylglucosaminyl-1-phosphotransferase. Inheritance: autosomal recessive. Synonym: pseudo-Hurler polydystrophy, pseudopolydystrophy. (05 Mar 2000) |
| mucolipidosis IV | <biochemistry> Psychomotor retardation with cloudy corneas and retinal degeneration, with inclusion cells in cultured fibroblasts; may be due to a deficiency of neuramidase, but details are uncertain. Inheritance: autosomal recessive. (05 Mar 2000) |
| mucolysis | The solution, digestion, or liquefaction of mucus. Origin: muco-+ G. Lysis, dissolution (05 Mar 2000) |
| mucolytic | Destroying or dissolving mucin, an agent that so acts: a mucopolysaccharide or glycoprotein, the chief constituent of mucus. Origin: Gr. Lysis = dissolution (18 Nov 1997) |
| mucomembranous | Relating to a mucous membrane. (05 Mar 2000) |
| mucomembranous enteritis | An affection of the intestinal mucous membrane characterised by constipation or diarrhoea (sometimes alternating), colic, and the passage of pseudomembranous shreds or incomplete casts of the intestine. Synonym: mucoenteritis. (05 Mar 2000) |
| muconate | <chemistry> A salt of muconic acid. Source: Websters Dictionary (01 Mar 1998) |
| muconate cycloisomerase | <enzyme> Do not confuse with 3-carboxy-cis,cis-muconate lactonizing enzyme Chemical name: 4-carboxy- methyl-4-hydroxyisocrotonolactone lyase(decycling) Registry number: EC 5.5.1.1 Synonym: cis,cis-muconate lactonizing enzyme, cis, cis-muconate cyclase (26 Jun 1999) |
| muconic | <chemistry> Of, pertaining to, or designating, an organic acid, obtained indirectly from mucic acid, and somewhat resembling itaconic acid. Origin: Mucic + itaconic. Source: Websters Dictionary (01 Mar 1998) |
| muconolactone delta-isomerase | <enzyme> Catalyses the conversion of 4-hydroxy-4-carboxymethylisocrotonolactone to 3-oxoadipate enol-lactone; minor descriptor (75-83); on-line and index medicus search isomerases (75-83) Registry number: EC 5.3.3.4 (26 Jun 1999) |
| mucopeptide | <protein> Synonym for peptidoglycan. (18 Nov 1997) |
| mucopeptide glycohydrolase | <cell biology, enzyme> Glycosidase that hydrolyses the bond between N acetyl muramic acid and N acetyl glucosamine, thus cleaving an important polymer of the cell wall of many bacteria. Present in tears, saliva and in the lysomes of phagocytic cells, it is an important antibacterial defence, particularly against gram-positive bacteria. (18 Nov 1997) |
| mucoperichondrial flap | A flap composed of mucosa and perichondrium, as from the nasal septum. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|---|---|---|---|
|
뮤코텐정 - 새창
|
영풍제약 |
A25055321 | Methyl N,S diacetylcysteinate | 일반의약품 | 급여 |
|
무코레바정 - 새창
|
구주제약 |
A27803941 | Rebamipide | 전문의약품 | 삭제 |
|
무코란정 - 새창
|
대한뉴팜 |
A60602891 | Rebamipide | 전문의약품 | 급여 |
|
뮤코핀정100mg - 새창
|
부광약품 |
A13102981 | Rebamipide | 전문의약품 | 급여 |
|
뮤코스판정 - 새창
|
서울제약 |
A37003191 | Hederae helicis Folia 30% Ethanol dried extract | 일반의약품 | 급여 |
|
무코메드정 - 새창
|
한국슈넬제약 |
A07104541 | Rebamipide | 전문의약품 | 삭제 |
|
무코바정 - 새창
|
넥스팜코리아 |
A66300431 | Rebamipide | 전문의약품 | 급여 |
|
뮤코렌정 - 새창
|
영일제약 |
A16604231 | Rebamipide | 전문의약품 | 삭제 |
|
뮤코실정 - 새창
|
한국웨일즈제약(주) |
A15204441 | Rebamipide | 전문의약품 | 삭제 |
| mucoid colony |
one that is large, dome-shaped, and shiny, containing large quantities of capsular polysaccharide material that may be drawn out in viscous strings by a needle; called also M c.
출처: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
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| mucus retention cyst |
a mucus-containing retention cyst caused by blockage of a salivary gland duct, visible as a small nodule on the oral mucosa; called also mucocele. Cf. mucus extravasation phenomenon, under phenomenon.
출처: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
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| mucocutaneous junction |
the site of transition between skin and mucous membrane.
출처: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
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| mucogingival junction |
a sharply scalloped, generally indistinct line running parallel with the free margin, separating the gingival tissue from that of the oral mucosa; visible under the microscope. Called also mucogingival line.
출처: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
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| mucoperiosteal flap |
a flap of mucosal tissue, including the periosteum, reflected from bone.
출처: www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspz...
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