4-hydroxyphenylpyruvate dioxygenase

4-hydroxyphenylpyruvate dioxygenase
4-hy·droxy·phen·yl·py·ru·vate di·oxy·gen·ase (hi-drok″se-fen″əl-piґroo-vāt di-okґsə-jən-ās) [EC 1.13.11.27] an enzyme of the oxidoreductase class that catalyzes the oxidation of p-hydroxyphenylpyruvate to homogentisate as a step in the use of tyrosine and phenylalanine as fuels. Deficiency of the enzyme due to heterozygous mutation in the gene encoding it causes hawkinsinuria; that due to homozygous mutation causes tyrosinemia type III.

Medical dictionary. 2011.

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  • Type III tyrosinemia — Infobox Disease Name = PAGENAME Caption = Tyrosine DiseasesDB = 29836 DiseasesDB mult = ICD10 = ICD10|E|70|2|e|70 ICD9 = ICD9|270.2 ICDO = OMIM = 276710 OMIM mult = MedlinePlus = eMedicineSubj = ped eMedicineTopic = 2339 MeshID = D020176 Type III …   Wikipedia

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  • Hawkinsinuria — Infobox Disease Name = PAGENAME Caption = Hawkinsin DiseasesDB = 29836 ICD10 = ICD9 = ICDO = OMIM = 276710 OMIM mult = OMIM2|140350 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = D020176 Hawkinsinuria, also called 4 Alpha… …   Wikipedia

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