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1 мукополисахаридоз I типа
type I mucopolysaccharidosis, Hurler's [Hurler-Pfaundler] syndrome, gargoylism, lipochondrodystrophy, Hurler's diseaseБольшой русско-английский медицинский словарь > мукополисахаридоз I типа
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2 мукополисахаридоз II типа
type II mucopolysaccharidosis, Hunter's syndromeБольшой русско-английский медицинский словарь > мукополисахаридоз II типа
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3 мукополисахаридоз III типа
type III mucopolysaccharidosis, Sanfilippo's syndromeБольшой русско-английский медицинский словарь > мукополисахаридоз III типа
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4 мукополисахаридоз IV типа
type IV mucopolysaccharidosis, Morquio's [Brailsford-Morquio] syndromeБольшой русско-английский медицинский словарь > мукополисахаридоз IV типа
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5 мукополисахаридоз V типа
type V mucopolysaccharidosis, Scheie's syndromeБольшой русско-английский медицинский словарь > мукополисахаридоз V типа
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6 мукополисахаридоз VI типа
type VI mucopolysaccharidosis, Maroteaux-Lamy syndromeБольшой русско-английский медицинский словарь > мукополисахаридоз VI типа
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7 мукополисахаридоз VII типа
type VII mucopolysaccharidosis, Sly's syndromeБольшой русско-английский медицинский словарь > мукополисахаридоз VII типа
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8 мукополисахаридоз I типа
Универсальный русско-английский словарь > мукополисахаридоз I типа
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9 болезнь Гурлера
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10 болезнь Пфаундлера-Гурлера
Medicine: lipochondrodystrophy, Pfaundler-Hurler syndrome, type IH mucopolysaccharidosis, mucopolysaccharidosis type I, alpha-L-iduronidase deficiency, Hurler-Scheie syndrome, IDUA deficiency, mucopolysaccharidosis I, Scheie syndrome, Pfaundler-Hurler disease, Hurler's disease, Hurler disease, Hurler syndromeУниверсальный русско-английский словарь > болезнь Пфаундлера-Гурлера
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11 болезнь Пфаундлера-Гурлера-Эллиса
Medicine: lipochondrodystrophy, Pfaundler-Hurler syndrome, type IH mucopolysaccharidosis, mucopolysaccharidosis type I, alpha-L-iduronidase deficiency, Hurler-Scheie syndrome, IDUA deficiency, mucopolysaccharidosis I, Scheie syndrome, Pfaundler-Hurler disease, Hurler's disease, Hurler disease, Hurler syndromeУниверсальный русско-английский словарь > болезнь Пфаундлера-Гурлера-Эллиса
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12 болезнь Шейе
1) Medicine: Hurler disease, lipochondrodystrophy, Pfaundler-Hurler syndrome, type IH mucopolysaccharidosis, mucopolysaccharidosis type I, alpha-L-iduronidase deficiency, Hurler-Scheie syndrome, IDUA deficiency, mucopolysaccharidosis I, Scheie syndrome, Pfaundler-Hurler disease, Hurler's disease2) Genetics: Hurler syndrome, Scheie disease, gargoilism -
13 мукополисахаридоз I
Универсальный русско-английский словарь > мукополисахаридоз I
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14 полидистрофия Гурлера-Эллиса
Medicine: lipochondrodystrophy, Pfaundler-Hurler syndrome, type IH mucopolysaccharidosis, mucopolysaccharidosis type I, alpha-L-iduronidase deficiency, Hurler-Scheie syndrome, IDUA deficiency, mucopolysaccharidosis I, Scheie syndrome, Pfaundler-Hurler disease, Hurler's disease, Hurler syndrome, Hurler diseaseУниверсальный русско-английский словарь > полидистрофия Гурлера-Эллиса
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15 болезнь Хантера
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16 мукополисахаридоз II типа
1) Medicine: Hunter syndrome, mucopolysaccharidosis type II2) Makarov: Hunter's syndrome, type II mucopolysaccharidosisУниверсальный русско-английский словарь > мукополисахаридоз II типа
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17 синдром Гунтера
Medicine: Hunter's syndrome (болезнь), mucopolysaccharidosis type II, type II mucopolysaccharidosis -
18 мукополисахаридоз III типа
Makarov: type III mucopolysaccharidosisУниверсальный русско-английский словарь > мукополисахаридоз III типа
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19 мукополисахаридоз IV типа
1) Medicine: Morquio's disease, Morquio syndrome2) Genetics: Morquio diseaseУниверсальный русско-английский словарь > мукополисахаридоз IV типа
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20 мукополисахаридоз V типа
Makarov: type V mucopolysaccharidosisУниверсальный русско-английский словарь > мукополисахаридоз V типа
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См. также в других словарях:
Mucopolysaccharidosis — MPS I redirects here. For zhuyin or bopomofo, a phonetic system for romanizing Chinese, also known as Mandarin Phonetic Symbols I, see Bopomofo. Mucopolysaccharidosis Classification and external resources ICD 10 E76 ICD 9 … Wikipedia
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… … Medical dictionary
Mucopolysaccharidosis (MPS) — One of a series of inherited metabolic disorders affecting a type of complex carbohydrate called a mucopolysaccharide that is deposited in body tissues because the person lacks the specific enzyme needed to metabolize it. The deposition of… … Medical dictionary
Ocular albinism type 1 — Classification and external resources ICD 10 E70.3 OMIM 300500 DiseasesDB … Wikipedia
MPS (mucopolysaccharidosis) — One of a series of inherited metabolic disorders affecting a type of complex carbohydrate called a mucopolysaccharide that is deposited in body tissues because the person lacks the specific enzyme needed to metabolize it. The deposition of… … Medical dictionary
List of diseases (M) — A list of diseases in the English wikipedia.DiseasesTOC MaMac* Mac Ardle disease * Mac Dermot Patton Williams syndrome * Mac Dermot Winter syndromeMaci Macr* Macias Flores Garcia Cruz Rivera syndrome * Mackay Shek Carr syndrome * Macleod Fraser… … Wikipedia
syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… … Medical dictionary
Coarse facial features — refer to a similar change in facial features in the advanced stage of certain conditions like Cretinism, Mucopolysaccharidoses etc, where affected individuals look remarkably similar due to the coarsening of their facial features. These typical… … Wikipedia
Chromosome 7 (human) — Chromosome 7 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 7 spans more than 158 million base pairs (the building material of DNA) and represents between 5 and 5.5 percent of the… … Wikipedia
Maroteaux-Lamy syndrome — Mucopolysaccharidosis type VI; deficiency of the lysosomal enzyme arylsulphatase B; resembles Hurler s disease in some respects … Dictionary of molecular biology
MPS IIIA — mucopolysaccharidosis III, type A … Medical dictionary
