- G6PD deficiency
- G6PD deficiency.(Источник: «Англо-русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд-во ВНИРО, 1995 г.)
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G6PD deficiency
Смотреть что такое "G6PD deficiency" в других словарях:
G6PD-Mangel — ICD 10 Codes G6PD Mangel (Glucose 6 phosphat Dehydrogenase Mangel) D55.0 Glucose 6 Phosphat Dehydrogenase (G6PD) Mangel mit Anämie E74.8 Glucose 6 Phosphat Dehydrogenase (G6PD) Mangel ohne Anämie Informationen in medizinischen Datenbanken OMIM… … Deutsch Wikipedia
Deficiency, glucose-6-phosphate dehydrogenase (G6PD) — Deficiency of G6PD is the commonest disease causing enzyme defect in humans affecting an estimated 400 million people. The G6PD gene is on the X chromosome. Males with the enzyme deficiency develop anemia due to breakup of their red blood cells… … Medical dictionary
Déficit en G6PD — Déficit en glucose 6 phosphate déshydrogénase Déficit en glucose 6 phosphate déshydrogénase Autre nom Favisme Référence MIM … Wikipédia en Français
Glucose-6-phosphate dehydrogenase deficiency — ] The discovery of G6PD deficiency relieved heavily upon the testing of prisoner volunteers at Illinois State Penitentiary, although today such studies cannot be performed. When some prisoners were given the drug primaquine, some developed… … Wikipedia
Pyruvate kinase deficiency — Infobox Disease Name = PAGENAME Caption = Phosphoenolpyruvate DiseasesDB = 11090 ICD10 = ICD10|D|55|2|d|55 ICD9 = ICD9|282.3 ICDO = OMIM = 266200 MedlinePlus = 001197 eMedicineSubj = med eMedicineTopic = 1980 MeshID = Pyruvate kinase deficiency,… … Wikipedia
glucose-6-phosphate dehydrogenase deficiency — a hereditary (X linked) condition in which the absence of the enzyme glucose 6 phosphate dehydrogenase (G6PD), which functions in carbohydrate metabolism, results in the breakdown of the red blood cells (haemolysis), usually after exposure to… … Medical dictionary
glucose-6-phosphate dehydrogenase deficiency — a hereditary (X linked) condition in which the absence of the enzyme glucose 6 phosphate dehydrogenase (G6PD), which functions in carbohydrate metabolism, results in the breakdown of the red blood cells (haemolysis), usually after exposure to… … The new mediacal dictionary
Glucose-6-phosphate dehydrogenase (G6PD) — Deficiency of G6PD is the commonest disease causing enzyme defect in humans affecting an estimated 400 million people. The G6PD gene is on the X chromosome. Males with the enzyme deficiency develop anemia due to breakup of their red blood cells… … Medical dictionary
glucose-6-phosphate dehydrogenase deficiency — n a hereditary metabolic disorder affecting red blood cells that is controlled by a variable gene on the X chromosome, that is characterized by a deficiency of glucose 6 phosphate dehydrogenase conferring marked susceptibility to hemolytic anemia … Medical dictionary
Glucose-6-Phosphat-Dehydrogenase-Mangel — ICD 10 Codes G6PD Mangel (Glucose 6 phosphat Dehydrogenase Mangel) D55.0 Glucose 6 Phosphat Dehydrogenase (G6PD) Mangel mit Anämie E74.8 Glucose 6 Phosphat Dehydrogenase (G6PD) Mangel ohne Anämie Informationen in medizinischen Datenbanken … Deutsch Wikipedia
