| mucoperichondrial flap | A flap composed of mucosa and perichondrium, as from the nasal septum. (05 Mar 2000) |
|---|---|
| mucoperiosteal | Relating to mucoperiosteum. (05 Mar 2000) |
| mucoperiosteal flap | A flap composed of mucosa and periosteum, as from the hard palate or gingiva. (05 Mar 2000) |
| mucoperiosteum | Mucous membrane and periosteum so intimately united as to form practically a single membrane, as that covering the hard palate. (05 Mar 2000) |
| mucopolysaccharidase | <chemical> Mixture of an "eliminase" and a glucuronidase Chemical name: lyase, mucopolysaccharide Synonym: thiomucase (26 Jun 1999) |
| mucopolysaccharide | <biochemistry> The polysaccharide components of proteoglycans, now more usually known as glycosaminoglycans. (18 Nov 1997) |
| mucopolysaccharide keratin dystrophy | A histologic finding seen in the surface epithelium of oral inflammatory fibrous hyperplasia, consisting of homogeneous eosinophilic pools of material in the superficial spinous layer. (05 Mar 2000) |
| mucopolysaccharidoses | Inherited diseases in humans resulting from inability to break down glycosaminoglycans. Hunter syndrome and Hurler syndrome, for example: result from defects in lysosomal enzymes needed to break down sulphated mucopolysaccharides. (18 Nov 1997) |
| mucopolysaccharidosis | Any of a group of lysosomal storage diseases that have in common a disorder in metabolism of mucopolysaccharides, as evidenced by excretion of various mucopolysaccharides in urine and infiltration of these substances into connective tissue, with resulting various defects of bone, cartilage, and connective tissue. (05 Mar 2000) |
| mucopolysaccharidosis I | Systemic lysosomal storage disease caused by a deficiency of alpha-l-iduronidase and characterised by progressive physical deterioration with urinary excretion of dermatan sulfate and heparan sulfate. There are three recognised phenotypes representing a spectrum of clinical severity from severe to mild: hurler's syndrome, hurler-scheie syndrome and scheie's syndrome (formerly mucopolysaccharidosis v). Symptoms may include dwarfism, hepatosplenomegaly, gargoyle-like facies, corneal clouding, cardiac complications, and noisy breathing. (12 Dec 1998) |
| mucopolysaccharidosis II | 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. (12 Dec 1998) |
| mucopolysaccharidosis III | Mucopolysaccharidosis characterised 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. (12 Dec 1998) |
| mucopolysaccharidosis IV | Genetic disorder of mucopolysaccharide metabolism characterised 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. (12 Dec 1998) |
| mucopolysaccharidosis vi | Mucopolysaccharidosis with excessive chondroitin sulfate b in urine, characterised by dwarfism and deafness. It is caused by a deficiency of n-acetylgalactosamine-4-sulfatase (arylsulfatase b). (12 Dec 1998) |
| mucopolysaccharidosis vii | Mucopolysaccharidosis characterised by excessive dermatan and heparan sulfates in the urine and hurler-like features. It is caused by a deficiency of beta-glucuronidase. (12 Dec 1998) |
Synonyms : ATP-Binding Cassette, Sub-Family C Proteins, MOAT Protein, Multispecific Organic Anion Transport Proteins, Multispecific Organic Anion Transporter, ATP Binding Cassette, Sub Family C Proteins, Multidrug Resistance Associated Protein
Synonyms : Complexes, Multienzyme
Synonyms : Oligogenic Traits, Polygenic Characters, Character, Polygenic, Characters, Polygenic, Inheritance, Multifactorial, Inheritance, Oligogenic, Inheritance, Polygenic, Inheritances, Multifactorial, Inheritances, Oligogenic, Inheritances, Polygenic, Oligogenic Trait
Synonyms : Cluster, Gene, Clusters, Gene, Families, Multigene, Family, Multigene, Gene Cluster, Gene, Reiterated, Multigene Families, Reiterated Gene, Reiterated Genes
Synonyms :
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|---|---|---|---|
|
무테린캅셀200mg - 새창
|
한국유나이티드제약 |
A12993541 | Acetylcysteine | 일반의약품 | 급여 |
|
무조날크림 - 새창
|
한미약품 |
A21402921 | Terbinafine HCl | 일반의약품 | 급여 |
|
뮤코라마캅셀 - 새창
|
대한약품공업 |
A02702781 | Glycerol iodide | 전문의약품 | 삭제 |
|
올소클론okt3주사액 - 새창
|
Ortho Biotech |
E02170031 | Muromonab-CD3 | 전문의약품 | 급여 | 분업예외의약품 |
|
뮤린티어스점안액 - 새창
|
일양약품 |
E01780031 | Polyvinyl Alcohol, Povidone | 일반의약품 | 비급여 |
|
무라노연고 - 새창
|
태극약품공업 |
A08601591 | Crotamiton, Hibiscus Cortex, Salicylic Acid, Tolnaftate | 일반의약품 | 비급여 |
|
물네오파스 - 새창
|
대일화학 |
Tocopherol Acetate | 일반의약품 | 비급여 |
|
|
머미루박스주 - 새창
|
녹십자 |
Live Attenuated Measles Vaccine, Mumps Virus Vaccine, Live, Rubella Virus Vaccine, Live | 전문의약품 | 미생산 |
|
|
멀터라민정 - 새창
|
홍익제약 |
Ascorbic Acid, Calcium pantothenate, Cyanocobalamin, Nicotinamide, Pyridoxine HCl, Riboflavin, Thiamine HCl | 일반의약품 | 비급여 |
|
|
뮤솔캅셀 - 새창
|
수도약품공업 |
A19202561 | Ambroxol HCl | 일반의약품 | 비급여 |
| mustard plaster |
a plaster containing powdered black mustard; applied to the skin as a counterirritant or rubefacient
출처: wordnet.princeton.edu/perl/webwn
|
|---|---|
| Mucorales |
an order of mostly saprophytic fungi
출처: wordnet.princeton.edu/perl/webwn
|
| mucilage |
a gelatinous substance secreted by plants glue: cement consisting of a sticky substance that is used as an adhesive
출처: wordnet.princeton.edu/perl/webwn
|
| multiple myeloma |
myeloma that develops in several places at the same time
출처: wordnet.princeton.edu/perl/webwn
|
| mucin |
a nitrogenous substance found in mucous secretions; a lubricant that protects body surfaces
출처: wordnet.princeton.edu/perl/webwn
|
| mu | North American coot |
|---|---|
| mu | having narrow flat sickle-shaped submerged fronds |
| mu | a mass of mud that a child has molded into the shape of pie |
| mu | grassy-leaved North American aquatic plant with yellow star-shaped blossoms |
| mu | a puddle of mud |
| mu | larval salamander of mountain lakes of Mexico that usually lives without metamorphosing |
| mu | large salamander of North American rivers and streams |
| mu | aquatic North American salamander with red feathery external gills |
| mu | a stain produced by mud |
| mu | bottom-dwelling freshwater turtle inhabiting muddy rivers of North and Central America |
| mu | covered with or as if with mud |
| mu | large catfish of central United States having a flattened head and projecting jaw |
