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 .
C10.228.140.163.100.435 Lysosomal Storage Diseases, Nervous System .
C10.228.140.163.100.435.825 Sphingolipidoses .
C10.228.140.163.100.435.825.700 Niemann-Pick Diseases .
C10.228.140.163.100.435.825.700.500 Niemann-Pick Disease, Type A .
C15 Hemic and Lymphatic Diseases .
C15.604 Lymphatic Diseases .
C15.604.250 Histiocytosis .
C15.604.250.410 Histiocytosis, Non-Langerhans-Cell .
C15.604.250.410.625 Niemann-Pick Diseases .
C15.604.250.410.625.500 Niemann-Pick Disease, Type A .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.435 Lysosomal Storage Diseases, Nervous System .
C16.320.565.189.435.825 Sphingolipidoses .
C16.320.565.189.435.825.700 Niemann-Pick Diseases .
C16.320.565.189.435.825.700.500 Niemann-Pick Disease, Type A .
C16.320.565.398 Lipid Metabolism, Inborn Errors .
C16.320.565.398.641 Lipidoses .
C16.320.565.398.641.803 Sphingolipidoses .
C16.320.565.398.641.803.730 Niemann-Pick Diseases .
C16.320.565.398.641.803.730.500 Niemann-Pick Disease, Type A .
C16.320.565.595 Lysosomal Storage Diseases .
C16.320.565.595.554 Lysosomal Storage Diseases, Nervous System .
C16.320.565.595.554.825 Sphingolipidoses .
C16.320.565.595.554.825.700 Niemann-Pick Diseases .
C16.320.565.595.554.825.700.500 Niemann-Pick Disease, Type A .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.435 Lysosomal Storage Diseases, Nervous System .
C18.452.132.100.435.825 Sphingolipidoses .
C18.452.132.100.435.825.700 Niemann-Pick Diseases .
C18.452.132.100.435.825.700.500 Niemann-Pick Disease, Type A .
C18.452.584 Lipid Metabolism Disorders .
C18.452.584.500 Dyslipidemias .
C18.452.584.500.500 Hyperlipidemias .
C18.452.584.687 Lipidoses .
C18.452.584.687.803 Sphingolipidoses .
C18.452.584.687.803.730 Niemann-Pick Diseases .
C18.452.584.687.803.730.500 Niemann-Pick Disease, Type A .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.435 Lysosomal Storage Diseases, Nervous System .
C18.452.648.189.435.825 Sphingolipidoses .
C18.452.648.189.435.825.700 Niemann-Pick Diseases .
C18.452.648.189.435.825.700.500 Niemann-Pick Disease, Type A .
C18.452.648.398 Lipid Metabolism, Inborn Errors .
C18.452.648.398.641 Lipidoses .
C18.452.648.398.641.803 Sphingolipidoses .
C18.452.648.398.641.803.730 Niemann-Pick Diseases .
C18.452.648.398.641.803.730.500 Niemann-Pick Disease, Type A .
C18.452.648.595 Lysosomal Storage Diseases .
C18.452.648.595.554 Lysosomal Storage Diseases, Nervous System .
C18.452.648.595.554.825 Sphingolipidoses .
C18.452.648.595.554.825.700 Niemann-Pick Diseases .
C18.452.648.595.554.825.700.500 Niemann-Pick Disease, Type A .
D02 Organic Chemicals .
D02.241 Carboxylic Acids .
D02.241.081 Acids, Acyclic .
D02.241.081.114 Butyrates .
D02.241.081.114.968 Isobutyrates .
D02.241.081.114.968.500 Fibric Acids .
D02.241.081.114.968.500.625 Fenofibrate .
D02.355 Ethers .
D02.355.726 Phenyl Ethers .
D02.355.726.305 Fibric Acids .
D02.355.726.305.625 Fenofibrate .
D02.455 Hydrocarbons .
D02.455.426 Hydrocarbons, Cyclic .
D02.455.426.559 Hydrocarbons, Aromatic .
D02.455.426.559.389 Benzene Derivatives .
D02.455.426.559.389.134 Benzophenones .
D02.455.426.559.389.134.750 Fenofibrate .
D02.455.426.559.389.657 Phenols .
D02.455.426.559.389.657.654 Phenyl Ethers .
D02.455.426.559.389.657.654.305 Fibric Acids .
D02.455.426.559.389.657.654.305.625 Fenofibrate .
D02.522 Ketones .
D02.522.223 Benzophenones .
D02.522.223.750 Fenofibrate .
D09 Carbohydrates .
D09.698 Polysaccharides .
D09.698.718 Polysaccharides, Bacterial .
D09.698.718.450 Lipopolysaccharides .
D09.698.718.450.500 Lipid A .
D10 Lipids .
D10.494 Lipopolysaccharides .
D10.494.500 Lipid A .
D23 Biological Factors .
D23.050 Antigens .
D23.050.161 Antigens, Bacterial .
D23.050.161.616 Polysaccharides, Bacterial .
D23.050.161.616.525 Lipopolysaccharides .
D23.050.161.616.525.500 Lipid A .
D23.946 Toxins, Biological .
D23.946.123 Bacterial Toxins .
D23.946.123.329 Endotoxins .
D23.946.123.329.500 Lipopolysaccharides .
D23.946.123.329.500.500 Lipid A .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Lipidoses .
Lipoidosis .
Lipidosis .
Lipoidoses .
Conditions characterized by abnormal lipid deposition due to disturbance in lipid metabolism, such as hereditary diseases involving lysosomal enzymes required for lipid breakdown. They are classified either by the enzyme defect or by the type of lipid involved. .
1.00
182576
 
Lipids .
Lipids and Antilipemic Agents .
A generic term for fats and lipoids, the alcohol-ether-soluble constituents of protoplasm, which are insoluble in water. They comprise the fats, fatty oils, essential oils, waxes, phospholipids, glycolipids, sulfolipids, aminolipids, chromolipids (lipochromes), and fatty acids. (Grant & Hackh's Chemical Dictionary, 5th ed) .
0.74
142894231
 
Fenofibrate .
Antara Micronized Procetofen .
Apo-Feno-Micro .
Apo-Fenofibrate .
CiL 8694 .
Controlip .
Fenobeta .
Fenofanton .
Fenofibrat AL .
Fenofibrat AZU .
Fenofibrat AbZ .
Fenofibrat FPh .
Fenofibrat Heumann .
Fenofibrat Hexal .
Fenofibrat Stada .
Fenofibrat-ratiopharm .
Fénofibrate Debat .
Fénofibrate MSD .
Gen-Fenofibrate .
LF-178 .
Lipanthyl .
Lipantil .
Liparison .
Lipidil .
Lipidil-Ter .
Livesan .
Lofibra .
MTW-Fenofibrat .
Normalip .
Novo-Fenofibrate .
Nu-Fenofibrate .
PMS-Fenofibrate Micro .
Phenofibrate .
Procetofene .
Secalip .
Supralip .
Tricor .
durafenat .
fenofibrat von ct .
AZU, Fenofibrat .
Apo Feno Micro .
Apo Fenofibrate .
Debat, Fénofibrate .
Fenofibrat ratiopharm .
Gen Fenofibrate .
Heumann, Fenofibrat .
Hexal, Fenofibrat .
LF 178 .
LF178 .
Lipidil Ter .
MTW Fenofibrat .
Micronized Procetofen, Antara .
Novo Fenofibrate .
Nu Fenofibrate .
PMS Fenofibrate Micro .
Procetofen, Antara Micronized .
Stada, Fenofibrat .
Procetofen .
LIPANTHYL .
An antilipemic agent which reduces both CHOLESTEROL and TRIGLYCERIDES in the blood. .
0.69
92393
 
Lipid A .
Lipid A is the biologically active component of lipopolysaccharides. It shows strong endotoxic activity and exhibits immunogenic properties. .
0.66
33424
 
Hyperlipidemias .
Hyperlipidemia .
Lipemia .
Lipidemia .
Hyperlipemias .
Lipemias .
Lipidemias .
Hyperlipemia .
Conditions with excess LIPIDS in the blood. .
0.65
70124372
 
Niemann-Pick Disease, Type A .
Classical Niemann-Pick Disease .
Neuronal Cholesterol Lipidosis .
Niemann-Pick Disease, Acute Neuronopathic Form .
Niemann-Pick Disease, Acute Neurovisceral Form .
Niemann-Pick Disease, Neuronopathic Type .
Niemann-Pick's Disease Type A .
Ophthalmoplegia, Supraoptic Vertical .
Sphingomyelin Cholesterol Lipidosis .
Sphingomyelin Lipidosis .
Sphingomyelinase Deficiency .
Type A Niemann-Pick Disease .
Cholesterol Lipidoses, Neuronal .
Cholesterol Lipidoses, Sphingomyelin .
Cholesterol Lipidosis, Neuronal .
Cholesterol Lipidosis, Sphingomyelin .
Classical Niemann Pick Disease .
Deficiencies, Sphingomyelinase .
Deficiency, Sphingomyelinase .
Lipidoses, Neuronal Cholesterol .
Lipidoses, Sphingomyelin .
Lipidoses, Sphingomyelin Cholesterol .
Lipidosis, Neuronal Cholesterol .
Lipidosis, Sphingomyelin .
Lipidosis, Sphingomyelin Cholesterol .
Neuronal Cholesterol Lipidoses .
Niemann Pick Disease, Acute Neuronopathic Form .
Niemann Pick Disease, Acute Neurovisceral Form .
Niemann Pick Disease, Neuronopathic Type .
Niemann Pick Disease, Type A .
Niemann Pick's Disease Type A .
Niemann-Pick Disease, Classical .
Ophthalmoplegias, Supraoptic Vertical .
Sphingomyelin Cholesterol Lipidoses .
Sphingomyelin Lipidoses .
Sphingomyelinase Deficiencies .
Sphingomyelinase Deficiency Diseases .
Supraoptic Vertical Ophthalmoplegia .
Supraoptic Vertical Ophthalmoplegias .
Type A Niemann Pick Disease .
Vertical Ophthalmoplegia, Supraoptic .
Vertical Ophthalmoplegias, Supraoptic .
Sphingomyelinase Deficiency Disease .
Classical Niemann-Pick Disease .
The classic infantile form of Niemann-Pick Disease, caused by mutation in SPHINGOMYELIN PHOSPHODIESTERASE. It is characterized by accumulation of SPHINGOMYELINS in the cells of the MONONUCLEAR PHAGOCYTE SYSTEM and other cell throughout the body leading to cell death. Clinical signs include JAUNDICE, hepatosplenomegaly, and severe brain damage. .
0.63
048