alkaptonuria
1alkaptonuria — alkaptonuria. См. алкаптонурия. (Источник: «Англо русский толковый словарь генетических терминов». Арефьев В.А., Лисовенко Л.А., Москва: Изд во ВНИРО, 1995 г.) …
2Alkaptonuria — Infobox Disease Name = PAGENAME Caption = Homogentisic acid Width = 180 DiseasesDB = 409 ICD10 = ICD10|E|70|2|e|70 ICD9 = ICD9|270.2 ICDO = OMIM = 203500 MedlinePlus = eMedicineSubj = ped eMedicineTopic = 64 MeshID = D000474 Alkaptonuria (black… …
3alkaptonuria — /al kap teuh noor ee euh, nyoor /, n. Pathol. excessive excretion of homogentisic acid in the urine, caused by a hereditary abnormality of the metabolism of tyrosine and phenylalanine. [1885 90; ALKAPTON + URIA] * * * ▪ pathology rather… …
4Alkaptonuria — aminorūgščių statusas T sritis embriologija atitikmenys: lot. Acidi aminoici; Alkaptonuria ryšiai: platesnis terminas – medžiagų apykaitos nepakankamumas sinonimas – alkaptonurija …
5alkaptonuria — Congenital absence of homogentisic acid oxidase, an enzyme that breaks down tyrosine and phenylalanine. Accumulation of homogentisic acid in homozygotes causes brown pigmentation of skin and eyes and damage to joints; urine blackens on standing …
6alkaptonuria — noun A rare inherited genetic disorder of phenylalanine and tyrosine metabolism, causing the accumulation and eventual excretion of alkapton …
7alkaptonuria — al·kap·ton·uria or al·cap·ton·uria (.)al .kap tə n(y)u̇rē ə n a rare recessive metabolic anomaly in humans marked by inability to complete the degradation of tyrosine and phenylalanine resulting in the presence of alkapton in the urine * * * n.… …
8alkaptonuria — n. disease characterized by alkapton in the urine …
9alkaptonuria — al·kap·ton·u·ria …
10alkaptonuria — n.; see alcaptonuria …