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hy·per·val·i·ne·mia (hi″pər-val″ĭ-neґme-ə) 1. an autosomal recessive aminoacidopathy, due to a defect in valine transaminase, characterized by elevated levels of valine in the plasma and urine with failure to thrive. 2. elevated levels of valine in the plasma. Called also valinemia.Medical dictionary. 2011.
hypervalinemia — hypervalinemia. См. гипервалинемия. (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.
Hypervalinemia — Infobox Disease Name = PAGENAME Caption = Valine DiseasesDB = ICD10 = ICD9 = ICD9|270.3 ICDO = OMIM = 277100 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Hypervalinemia (occasionally called valinemia) is a rare autosomal recessive… … Wikipedia
гипервалинемия — hypervalinemia гипервалинемия. НЗЧ, характеризующееся нарушением обмена валина, ведущее к психическим расстройствам; наследуется по аутосомно рецессивному типу. (Источник: «Англо русский толковый словарь генетических терминов». Арефьев В.А.,… … Молекулярная биология и генетика. Толковый словарь.
maple syrup urine disease — ▪ pathology inherited metabolic disorder involving leucine, isoleucine, and valine (a group of branch chain amino acids). Normally, these amino acids are metabolized, step by step, by a number of enzymes, each of which is specific for each… … Universalium
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