Diseases in biochemistry 1

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Revision as of 15:33, 5 January 2023 by Nikolas (talk | contribs) (Created page with "{| class="wikitable" |'''Disease''' |'''Affected enzyme(s)''' |- |Alkaptonuria |Homogentisate 1,2-dioxygenase |- |Fructosemia |Fructose 1-phosphate aldolase |- |Fructosuria |Fructokinase |- |Phenylketonuria |Phenylalanine hydroxylase |- |Maple syrup urine disease |Branched-chain α-ketoacid dehydrogenase complex |- |Tyrosinemia type I |Fumarylacetoacetase |- |Tyrosinemia type II |Tyrosine aminotransferase |- |Tyorsinemia type III |p-hydroxyphenylpyruvate dioxygenase |- |...")
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Disease Affected enzyme(s)
Alkaptonuria Homogentisate 1,2-dioxygenase
Fructosemia Fructose 1-phosphate aldolase
Fructosuria Fructokinase
Phenylketonuria Phenylalanine hydroxylase
Maple syrup urine disease Branched-chain α-ketoacid dehydrogenase complex
Tyrosinemia type I Fumarylacetoacetase
Tyrosinemia type II Tyrosine aminotransferase
Tyorsinemia type III p-hydroxyphenylpyruvate dioxygenase
Homocystinuria Cystathione β-synthase
Hyperargininemia Arginase
Lesch-Nyhan syndrome Hypoxanthine-guanine phosphoribosyltransferase
Argininosuccinate lyase deficiency Argininosuccinate lyase
Βeta-ketothiolase deficiency Acyl-CoA acetyltransferase
Methylmalonic acidemia Methylmalonic-CoA mutase
Propionic acidemia Propionyl-CoA carboxylase
Disease that leads to cataract Aldose reductase with galactose
Galactosemia Galactokinase

Galactose 1-phosphate uridyltransferase

UDP-galactose 4-epimerase

McArdle’s disease Glycogen phosphorylase
Cori’s disease Glucosidase activity of glycogen debranching enzyme
Albinism Tyrosinase