serw-MX  [xml]  
 


    
 DeCS Categories

B01 Eukaryota .
B01.650 Plants .
B01.650.940 Viridiplantae .
B01.650.940.800 Streptophyta .
B01.650.940.800.575 Embryophyta .
B01.650.940.800.575.912 Tracheophyta .
B01.650.940.800.575.912.250 Magnoliopsida .
B01.650.940.800.575.912.250.859 Rosanae .
B01.650.940.800.575.912.250.859.937 Rosales .
B01.650.940.800.575.912.250.859.937.844 Ulmaceae .
C06 Digestive System Diseases .
C06.552 Liver Diseases .
C06.552.970 Zellweger Syndrome .
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 .
C10.228.140.163.100.968 Zellweger Syndrome .
C12 Male Urogenital Diseases .
C12.777 Urologic Diseases .
C12.777.419 Kidney Diseases .
C12.777.419.978 Zellweger Syndrome .
C13 Female Urogenital Diseases and Pregnancy Complications .
C13.351 Female Urogenital Diseases .
C13.351.968 Urologic Diseases .
C13.351.968.419 Kidney Diseases .
C13.351.968.419.978 Zellweger Syndrome .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.077 Abnormalities, Multiple .
C16.131.077.970 Zellweger Syndrome .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.968 Zellweger Syndrome .
C16.320.565.663 Peroxisomal Disorders .
C16.320.565.663.970 Zellweger Syndrome .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.968 Zellweger Syndrome .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.968 Zellweger Syndrome .
C18.452.648.663 Peroxisomal Disorders .
C18.452.648.663.970 Zellweger Syndrome .
D02 Organic Chemicals .
D02.092 Amines .
D02.092.471 Ethylamines .
D02.092.471.683 Phenethylamines .
D02.092.471.683.915 Selegiline .
D03 Heterocyclic Compounds .
D03.383 Heterocyclic Compounds, 1-Ring .
D03.383.725 Pyridines .
D03.383.725.620 Pheniramine .
D03.383.725.620.129 Brompheniramine .
D03.383.725.620.129.960 Zimeldine .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Ulmaceae .
Celti .
Hackberries .
Zelkovas .
Celtis .
Hackberry .
Zelkova .
A plant family of the order Urticales, subclass Hamamelidae, class Magnoliopsida. Members are trees and shrubs of temperate regions that have watery sap and alternate leaves which are lopsided at the base. The flowers lack petals. .
1.00
860
 
Zimeldine .
H-102-09 .
Zelmid .
Zimeldine Hydrochloride .
Zimelidin .
Zimelidine Hydrochloride .
H 102 09 .
H10209 .
Hydrochloride, Zimeldine .
Hydrochloride, Zimelidine .
Zimelidine .
One of the SEROTONIN UPTAKE INHIBITORS formerly used for depression but was withdrawn worldwide in September 1983 because of the risk of GUILLAIN-BARRE SYNDROME associated with its use. (From Martindale, The Extra Pharmacopoeia, 29th ed, p385) .
0.58
2466
 
Selegiline .
E-250 .
Eldepryl .
Emsam .
Humex .
Jumex .
L-Deprenyl .
Selegiline Hydrochloride .
Selegiline Hydrochloride, (R)-Isomer .
Selegiline Hydrochloride, (R,S)-Isomer .
Selegiline Hydrochloride, (S)-Isomer .
Selegiline, (R)-Isomer .
Selegiline, (R,S)-Isomer .
Selegiline, (S)-Isomer .
Selegyline .
Yumex .
Zelapar .
E 250 .
E250 12584 .
Hydrochloride, Selegiline .
Deprenalin .
Deprenil .
Deprenyl .
A selective, irreversible inhibitor of Type B monoamine oxidase. It is used in newly diagnosed patients with Parkinson's disease. It may slow progression of the clinical disease and delay the requirement for levodopa therapy. It also may be given with levodopa upon onset of disability. (From AMA Drug Evaluations Annual, 1994, p385) The compound without isomeric designation is Deprenyl. .
0.58
222280
 
Zellweger Syndrome .
Cerebro-Hepato-Renal Syndrome .
PBD, ZSS .
Peroxisome Biogenesis Disorders, Zellweger Syndrome Spectrum .
Zellweger Disease .
Zellweger Spectrum .
Zellweger Syndrome Spectrum .
Zellweger's Syndrome .
Cerebro Hepato Renal Syndrome .
Spectrum, Zellweger .
Zellweger Like Syndrome .
Cerebrohepatorenal Syndrome .
Zellweger-Like Syndrome .
An autosomal recessive disorder due to defects in PEROXISOME biogenesis which involves more than 13 genes encoding peroxin proteins of the peroxisomal membrane and matrix. Zellweger syndrome is typically seen in the neonatal period with features such as dysmorphic skull; MUSCLE HYPOTONIA; SENSORINEURAL HEARING LOSS; visual compromise; SEIZURES; progressive degeneration of the KIDNEYS and the LIVER. Zellweger-like syndrome refers to phenotypes resembling the neonatal Zellweger syndrome but seen in children or adults with apparently intact peroxisome biogenesis. .
0.41
4555