serw-MX  [xml]  
 


    
 DeCS Categories

C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.163 Brain Diseases, Metabolic .
C10.228.140.163.100 Brain Diseases, Metabolic, Inborn .
C10.228.140.163.100.365 Homocystinuria .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.100 Amino Acid Metabolism, Inborn Errors .
C16.320.565.100.480 Hyperhomocysteinemia .
C16.320.565.100.480.500 Homocystinuria .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.365 Homocystinuria .
C17 Skin and Connective Tissue Diseases .
C17.300 Connective Tissue Diseases .
C17.300.428 Homocystinuria .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.365 Homocystinuria .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.100 Amino Acid Metabolism, Inborn Errors .
C18.452.648.100.480 Hyperhomocysteinemia .
C18.452.648.100.480.500 Homocystinuria .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.365 Homocystinuria .
D02 Organic Chemicals .
D02.886 Sulfur Compounds .
D02.886.030 Amino Acids, Sulfur .
D02.886.030.498 Homocysteine .
D02.886.030.554 Homocystine .
D08 Enzymes and Coenzymes .
D08.811 Enzymes .
D08.811.913 Transferases .
D08.811.913.555 One-Carbon Group Transferases .
D08.811.913.555.500 Methyltransferases .
D08.811.913.555.500.625 Homocysteine S-Methyltransferase .
D12 Amino Acids, Peptides, and Proteins .
D12.125 Amino Acids .
D12.125.095 Amino Acids, Diamino .
D12.125.095.533 Homocystine .
D12.125.119 Amino Acids, Dicarboxylic .
D12.125.119.658 Homocystine .
D12.125.166 Amino Acids, Sulfur .
D12.125.166.498 Homocysteine .
D12.125.166.554 Homocystine .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Homocysteine .
Homocysteine, L-Isomer .
2 amino 4 mercaptobutyric acid .
Homocysteine, L Isomer .
L-Isomer Homocysteine .
2-amino-4-mercaptobutyric acid .
A thiol-containing amino acid formed by a demethylation of METHIONINE. .
1.00
20513514
 
Homocystine .
0.85
1484
 
Homocystinuria .
Cystathionine Beta Synthase Deficiency .
Deficiency Disease, Cystathionine beta-Synthase .
CBS Deficiencies .
Cystathionine beta Synthase Deficiency Disease .
Deficiencies, CBS .
Deficiency Disease, Cystathionine beta Synthase .
Deficiency, CBS .
Cystathionine beta-Synthase Deficiency Disease .
CBS Deficiency .
Autosomal recessive inborn error of methionine metabolism usually caused by a deficiency of CYSTATHIONINE BETA-SYNTHASE and associated with elevations of homocysteine in plasma and urine. Clinical features include a tall slender habitus, SCOLIOSIS, arachnodactyly, MUSCLE WEAKNESS, genu varus, thin blond hair, malar flush, lens dislocations, an increased incidence of MENTAL RETARDATION, and a tendency to develop fibrosis of arteries, frequently complicated by CEREBROVASCULAR ACCIDENTS and MYOCARDIAL INFARCTION. (From Adams et al., Principles of Neurology, 6th ed, p979) .
0.70
281574
 
Homocysteine S-Methyltransferase .
Homocysteine Methyltransferase .
Homocysteine Transmethylase .
S-Adenosylmethionine Homocysteine Methyltransferase .
S-Methylmethionine Homocysteine Methyltransferase .
Homocysteine Methyltransferase, S-Adenosylmethionine .
Homocysteine Methyltransferase, S-Methylmethionine .
Homocysteine S Methyltransferase .
Methyltransferase, Homocysteine .
Methyltransferase, S-Adenosylmethionine Homocysteine .
Methyltransferase, S-Methylmethionine Homocysteine .
S Adenosylmethionine Homocysteine Methyltransferase .
S Methylmethionine Homocysteine Methyltransferase .
S-Methyltransferase, Homocysteine .
Transmethylase, Homocysteine .
An enzyme that catalyzes the demethylation of L-homocysteine to L-METHIONINE. .
0.68
041