- nounany of a group of genetic disorders involving a defect in the metabolism of mucopolysaccharides resulting in greater than normal levels of mucopolysaccharides in tissues• Hypernyms:↑genetic disease, ↑genetic disorder, ↑genetic abnormality, ↑genetic defect, ↑congenital disease, ↑inherited disease, ↑inherited disorder, ↑hereditary disease, ↑hereditary condition
Useful english dictionary. 2012.
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mucopolysaccharidosis — mucopolysaccharidosis. См. мукополисахаридозы. (Источник: «Англо русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд во ВНИРО, 1995 г.) … Молекулярная биология и генетика. Толковый словарь.
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 VI — Infobox Disease Name = PAGENAME Caption = DiseasesDB = ICD10 = ICD10|E|76|2|e|70 ICD9 = ICD9|277.5 ICDO = OMIM = 253200 MedlinePlus = eMedicineSubj = ped eMedicineTopic = 1373 MeshID = D009087 Mucopolysaccharidosis VI (or Maroteaux Lamy disease)… … 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 — (= mucopolysaccharidoses (plural) ) Inherited diseases in humans resulting from inability to break down glycosaminoglycans. Hunter syndrome and Hurler s disease, for example, result from defects in lysosomal enzymes needed to break down sulphated … Dictionary of molecular biology
mucopolysaccharidosis — noun Any of a group of metabolic disorders caused by the absence or malfunction of lysosomal enzymes needed to break down glycosaminoglycans … Wiktionary
mucopolysaccharidosis I — (MPS I) originally, Hurler syndrome; the term now encompasses any of the forms characterized by deficiency of L iduronidase and excretion in the urine of dermatan sulfate and heparan sulfate … Medical dictionary
mucopolysaccharidosis IH — (MPS I H) Hurler syndrome … Medical dictionary
mucopolysaccharidosis IH/S — (MPS I H/S) Hurler Scheie syndrome … Medical dictionary
mucopolysaccharidosis IS — (MPS I S) Scheie syndrome … Medical dictionary
mucopolysaccharidosis II — (MPS II) Hunter syndrome … Medical dictionary