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・ Tyrosine 2,3-aminomutase
・ Tyrosine aminotransferase
・ Tyrosine ammonia-lyase
・ Tyrosine decarboxylase
・ Tyrosine hydroxylase
・ Tyrosine kinase
・ Tyrosine kinase 2
・ Tyrosine N-monooxygenase
・ Tyrosine phenol-lyase
・ Tyrosine phosphorylation
・ Tyrosine sulfation
・ Tyrosine-ester sulfotransferase
・ Tyrosine-kinase inhibitor
・ Tyrosine-protein kinase BLK
・ Tyrosine-protein kinase CSK
Tyrosinemia
・ Tyrosinemia type II
・ Tyrosinemia type III
・ Tyrosine—arginine ligase
・ Tyrosine—tRNA ligase
・ Tyrosol
・ Tyrosylprotein sulfotransferase
・ Tyrothricin
・ Tyrotoxism
・ Tyrowo
・ TYRP1
・ Tyrrau Mawr
・ Tyrraz
・ Tyrrell
・ Tyrrell & Green


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Tyrosinemia : ウィキペディア英語版
Tyrosinemia

Tyrosinemia (or "Tyrosinaemia") is an error of metabolism, usually inborn, in which the body cannot effectively break down the amino acid tyrosine. Symptoms include liver and kidney disturbances and mental retardation. Untreated, tyrosinemia can be fatal.
Most inborn forms of tyrosinemia produce hypertyrosinemia (high levels of tyrosine).〔
Charles Scriver, Beaudet, A.L., Valle, D., Sly, W.S., Vogelstein, B., Childs, B., Kinzler, K.W. (Accessed 2007). (The Online Metabolic and Molecular Bases of Inherited Disease. ) Chapter 79. New York: McGraw-Hill.〕
==Types==
There are three types of tyrosinemia, each with distinctive symptoms and caused by the deficiency of a different enzyme.
* Type I tyrosinemia
* Type II tyrosinemia
* Type III tyrosinemia

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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