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Biochemistry Amino Acid Metabolic Disorder 0a0dda29

Enzyme dificient in alkaptonuria -

A
Kynureninase
B
Tyrosine hydroxylase
C
Homogentisate oxidase
D
Tyrosinase
High-Yield Explanation
Ans. is 'c' i.e., Homogentisate oxidase Metabolic diseaseEnzyme deficientMaple syrup urine diseaseBranched chain ketoacid dehydrogenaseMethyl-melonic aciduriaMethyl-malonyl CoA mutase (isomerase)Sweaty feet odor in bodyIsovaleryl-CoA dehydrogenaseTvrosinemia I (Tyrosinosis)Fumarylacetoacetate hydroxylaseTyrosinemia IITyrosine transaminase (Tyrosine aminotransferase)Neonatal tyrosinemiaHydroxyphenyl pyruvate hydroxylaseAlbinismTyrosinaseAlkaptonuriaHomogentisate oxidasePhenylketonuriaPhenylalanine hydroxylaseOrotic aciduriaOMP decarboxylaseHomocystinuriaCystathionine svnthataseLesh-Nyhan syndromeComplete deficiency of enzyme HGPRTCystinosisCystine reductase

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