serw-MX  [xml]  
 


    
 DeCS Categories

B03 Bacteria .
B03.370 Fusobacteria .
B03.370.600 Propionigenium .
B03.440 Gram-Negative Bacteria .
B03.440.425 Gram-Negative Anaerobic Bacteria .
B03.440.425.410 Gram-Negative Anaerobic Straight, Curved, and Helical Rods .
B03.440.425.410.600 Propionigenium .
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 .
C16.320.565.100.823 Propionic Acidemia .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.100 Amino Acid Metabolism, Inborn Errors .
C18.452.648.100.823 Propionic Acidemia .
D02 Organic Chemicals .
D02.092 Amines .
D02.092.471 Ethylamines .
D02.092.471.308 Diethylpropion .
D02.241 Carboxylic Acids .
D02.241.081 Acids, Acyclic .
D02.241.081.751 Propionates .
D02.540 Lactones .
D02.540.600 Propiolactone .
D03 Heterocyclic Compounds .
D03.383 Heterocyclic Compounds, 1-Ring .
D03.383.725 Pyridines .
D03.383.725.791 Pyridones .
D03.383.725.791.496 Iodopyridones .
D03.383.725.791.496.750 Propyliodone .
D10 Lipids .
D10.251 Fatty Acids .
D10.251.400 Fatty Acids, Volatile .
D10.251.400.706 Propionates .
D12 Amino Acids, Peptides, and Proteins .
D12.776 Proteins .
D12.776.097 Bacterial Proteins .
D12.776.097.120 Bacterial Outer Membrane Proteins .
D12.776.097.120.425 Fimbriae Proteins .
D12.776.543 Membrane Proteins .
D12.776.543.100 Bacterial Outer Membrane Proteins .
D12.776.543.100.300 Fimbriae Proteins .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Diethylpropion .
2-Diethylaminopropiophenone .
Amfepramone .
Anorex .
Delgamer .
Diethylpropion Hydrochloride .
Dietil-retard .
Ifa Norex .
Lipomin .
Maruate .
Modératan .
Neobes .
Nobesine .
Phepranon .
Propion .
Préfamone .
Regenon .
Regibon .
Tenuate .
Tepanil .
Dietil retard .
Dietilretard .
Hydrochloride, Diethylpropion .
Norex, Ifa .
Amfepramon .
A appetite depressant considered to produce less central nervous system disturbance than most drugs in this therapeutic category. It is also considered to be among the safest for patients with hypertension. (From AMA Drug Evaluations Annual, 1994, p2290) .
1.00
 
Propionates .
Propanoates .
Propanoic Acid Derivatives .
Propanoic Acids .
Propionic Acid Derivatives .
Propionic Acids .
Acids, Propanoic .
Acids, Propionic .
Derivatives, Propanoic Acid .
Derivatives, Propionic Acid .
Propionic Acids .
Derivatives of propionic acid. Included under this heading are a broad variety of acid forms, salts, esters, and amides that contain the carboxyethane structure. .
0.81
 
Propyliodone .
Dionosil .
Gastrotrast .
Propiodone .
Radiopaque medium usually in oil; used in bronchography. .
0.72
 
Propionigenium .
A genus of strictly anaerobic, nonsporeforming gram-negative bacteria in the family Fusobacteriaceae. Species in this genus are popularly used in biochemical research. .
0.68
 
Propiolactone .
beta Propiolactone .
beta-Propiolactone .
Propanolide .
Disinfectant used in vapor form to sterilize vaccines, grafts, etc. The vapor is very irritating and the liquid form is carcinogenic. .
0.66
 
Fimbriae Proteins .
Fimbriae Protein Precusors .
Pili Structural Proteins .
Pilin Precursors .
Pilins .
Pre-Pilin .
Sex Pili Structural Proteins .
Pre Pilin .
Precursors, Pilin .
Precusors, Fimbriae Protein .
Protein Precusors, Fimbriae .
Pilin .
Propilin .
Proteins that are structural components of bacterial fimbriae (FIMBRIAE, BACTERIAL) or sex pili (PILI, SEX). .
0.63
 
Propionic Acidemia .
Acidemia Propionic .
Hyperglycinemia With Ketoacidosis And Leukopenia .
Propionic Aciduria .
Propionicaciduria .
Acidemia Propionics .
Acidemia, Propionic .
Acidemias, Propionic .
Aciduria, Propionic .
Acidurias, Propionic .
Carboxylase Deficiencies, Propionyl-CoA .
Carboxylase Deficiency, Propionyl-CoA .
Deficiencies, PCC .
Deficiencies, Propionyl-CoA Carboxylase .
Deficiency, PCC .
Deficiency, Propionyl-CoA Carboxylase .
Glycinemias, Ketotic .
Hyperglycinemia, Ketotic .
Hyperglycinemias, Ketotic .
Ketotic Glycinemias .
Ketotic Hyperglycinemias .
PCC Deficiencies .
Propionic Acidemias .
Propionic Acidurias .
Propionic, Acidemia .
Propionicacidemias .
Propionicacidurias .
Propionics, Acidemia .
Propionyl CoA Carboxylase Deficiency .
Propionyl-CoA Carboxylase Deficiencies .
Glycinemia, Ketotic .
Ketotic Glycinemia .
Ketotic Hyperglycinemia .
PCC Deficiency .
Propionicacidemia .
Propionyl-CoA Carboxylase Deficiency .
Autosomal recessive metabolic disorder caused by mutations in PROPIONYL-COA CARBOXYLASE genes that result in dysfunction of branch chain amino acids and of the metabolism of certain fatty acids. Neonatal clinical onset is characterized by severe metabolic acidemia accompanied by hyperammonemia, HYPERGLYCEMIA, lethargy, vomiting, HYPOTONIA; and HEPATOMEGALY. Survivors of the neonatal onset propionic acidemia often show developmental retardation, and intolerance to dietary proteins. Late-onset form of the disease shows mild mental and/or developmental retardation, sometimes without metabolic acidemia. .
0.63