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 DeCS Categories

C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.831 Skin Abnormalities .
C16.131.831.512 Ichthyosis .
C16.131.831.512.723 Sjogren-Larsson Syndrome .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.398 Lipid Metabolism, Inborn Errors .
C16.320.565.398.641 Lipidoses .
C16.320.565.398.641.723 Sjogren-Larsson Syndrome .
C16.320.850 Skin Diseases, Genetic .
C16.320.850.820 Sjogren-Larsson Syndrome .
C16.614 Infant, Newborn, Diseases .
C16.614.492 Ichthyosis .
C16.614.492.723 Sjogren-Larsson Syndrome .
C17 Skin and Connective Tissue Diseases .
C17.800 Skin Diseases .
C17.800.428 Keratosis .
C17.800.428.333 Ichthyosis .
C17.800.428.333.723 Sjogren-Larsson Syndrome .
C17.800.804 Skin Abnormalities .
C17.800.804.512 Ichthyosis .
C17.800.804.512.723 Sjogren-Larsson Syndrome .
C17.800.827 Skin Diseases, Genetic .
C17.800.827.820 Sjogren-Larsson Syndrome .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.584 Lipid Metabolism Disorders .
C18.452.584.687 Lipidoses .
C18.452.584.687.723 Sjogren-Larsson Syndrome .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.398 Lipid Metabolism, Inborn Errors .
C18.452.648.398.641 Lipidoses .
C18.452.648.398.641.723 Sjogren-Larsson Syndrome .
D08 Enzymes and Coenzymes .
D08.811 Enzymes .
D08.811.682 Oxidoreductases .
D08.811.682.047 Alcohol Oxidoreductases .
D08.811.682.047.150 Carbohydrate Dehydrogenases .
D08.811.682.047.150.700 Sugar Alcohol Dehydrogenases .
D08.811.682.047.820 NAD (+) and NADP (+) Dependent Alcohol Oxidoreductases .
D08.811.682.047.820.250 Alcohol Dehydrogenase .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Alcohol Oxidoreductases .
Carbonyl Reductases .
Ketone Reductases .
Oxidoreductases, Alcohol .
Reductases, Carbonyl .
Reductases, Ketone .
A subclass of enzymes which includes all dehydrogenases acting on primary and secondary alcohols as well as hemiacetals. They are further classified according to the acceptor which can be NAD+ or NADP+ (subclass 1.1.1), cytochrome (1.1.2), oxygen (1.1.3), quinone (1.1.5), or another acceptor (1.1.99). .
1.00
1412371
 
Alcohol Dehydrogenase .
Alcohol Dehydrogenase (NAD+) .
Alcohol Dehydrogenase I .
Alcohol Dehydrogenase II .
Alcohol-NAD+ Oxidoreductase .
Yeast Alcohol Dehydrogenase .
Alcohol Dehydrogenase, Yeast .
Alcohol NAD+ Oxidoreductase .
Dehydrogenase, Alcohol .
Dehydrogenase, Yeast Alcohol .
Oxidoreductase, Alcohol-NAD+ .
A zinc-containing enzyme which oxidizes primary and secondary alcohols or hemiacetals in the presence of NAD. In alcoholic fermentation, it catalyzes the final step of reducing an aldehyde to an alcohol in the presence of NADH and hydrogen. .
0.89
216238
 
Sugar Alcohol Dehydrogenases .
Alcohol Dehydrogenases, Sugar .
Alcohol Oxidoreductases, Sugar .
Dehydrogenases, Sugar Alcohol .
Oxidoreductases, Sugar Alcohol .
Sugar Alcohol Oxidoreductases .
Reversibly catalyzes the oxidation of a hydroxyl group of sugar alcohols to form a keto sugar, aldehyde or lactone. Any acceptor except molecular oxygen is permitted. Includes EC 1.1.1.; EC 1.1.2. and EC 1.1.99. .
0.84
21438
 
Oxidoreductases .
Dehydrogenase .
Oxidase .
Reductase .
Dehydrogenases .
Oxidases .
Reductases .
The class of all enzymes catalyzing oxidoreduction reactions. The substrate that is oxidized is regarded as a hydrogen donor. The systematic name is based on donor:acceptor oxidoreductase. The recommended name will be dehydrogenase, wherever this is possible; as an alternative, reductase can be used. Oxidase is only used in cases where O2 is the acceptor. (Enzyme Nomenclature, 1992, p9) .
0.77
10836189
 
Sjogren-Larsson Syndrome .
Congenital Icthyosis Mental Retardation Spasticity Syndrome .
FALDH Deficiency .
Fatty Alcohol:NAD+ Oxidoreductase Deficiency .
Fatty Aldehyde Dehydrogenase Deficiency .
Fatty Aldehyde Dehydrogenase Deficiency Disease .
Ichthyosis Oligophrenia Syndrome .
Ichthyosis, Spastic Neurologic Disorder, and Oligophrenia .
Sjögren-Larsson Syndrome .
Sjogren Larsson Syndrome .
An autosomal recessive neurocutaneous disorder characterized by severe ichthyosis MENTAL RETARDATION; SPASTIC PARAPLEGIA; and congenital ICHTHYOSIS. It is caused by mutation of gene encoding microsomal fatty ALDEHYDE DEHYDROGENASE leading to defect in fatty alcohol metabolism. .
0.67
6207