serw-MX  [xml]  
 


    
 DeCS Categories

C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.850 Skin Diseases, Genetic .
C16.320.850.190 Darier Disease .
C17 Skin and Connective Tissue Diseases .
C17.800 Skin Diseases .
C17.800.428 Keratosis .
C17.800.428.275 Darier Disease .
C17.800.827 Skin Diseases, Genetic .
C17.800.827.190 Darier Disease .
D02 Organic Chemicals .
D02.033 Alcohols .
D02.033.100 Amino Alcohols .
D02.033.100.291 Ethanolamines .
D02.033.100.291.805 Sotalol .
D02.065 Amides .
D02.065.884 Sulfonamides .
D02.065.884.438 Darunavir .
D02.065.884.485 Dichlorphenamide .
D02.092 Amines .
D02.092.063 Amino Alcohols .
D02.092.063.291 Ethanolamines .
D02.092.063.291.805 Sotalol .
D02.092.146 Aniline Compounds .
D02.092.146.271 Bromhexine .
D02.092.384 Cyclohexylamines .
D02.092.384.175 Bromhexine .
D02.241 Carboxylic Acids .
D02.241.081 Acids, Acyclic .
D02.241.081.251 Carbamates .
D02.241.081.251.222 Darunavir .
D02.241.081.751 Propionates .
D02.241.081.751.120 Dextropropoxyphene .
D02.886 Sulfur Compounds .
D02.886.590 Sulfones .
D02.886.590.700 Sulfonamides .
D02.886.590.700.400 Darunavir .
D02.886.590.700.410 Dichlorphenamide .
D03 Heterocyclic Compounds .
D03.383 Heterocyclic Compounds, 1-Ring .
D03.383.312 Furans .
D03.383.312.303 Darunavir .
D03.383.742 Pyrimidines .
D03.383.742.675 Pyrimethamine .
D08 Enzymes and Coenzymes .
D08.811 Enzymes .
D08.811.913 Transferases .
D08.811.913.696 Phosphotransferases .
D08.811.913.696.620 Phosphotransferases (Alcohol Group Acceptor) .
D08.811.913.696.620.682 Protein Kinases .
D08.811.913.696.620.682.700 Protein-Serine-Threonine Kinases .
D08.811.913.696.620.682.700.534 Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 .
D12 Amino Acids, Peptides, and Proteins .
D12.776 Proteins .
D12.776.637 Parkinson Disease Associated Proteins .
D12.776.637.750 Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 .
G01 Physical Phenomena .
G01.590 Optical Phenomena .
G01.590.540 Light .
G01.590.540.233 Darkness .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Bromhexine .
Aparsonin .
Bisolvon .
Bromhexin .
Bromhexin BC .
Bromhexin Berlin-Chemie .
Bromhexin-ratiopharm .
Bromhexine Hydrochloride .
Bromhexine Monohydrochloride .
Brotussol .
Darolan .
Dur-Elix .
Famel Bromhexine .
Flegamin .
Flubron .
Hustentabs-ratiopharm .
Mucohexine .
NA-274 .
Quentan .
Tesacof .
bromhexin von ct .
BC, Bromhexin .
Bromhexin Berlin Chemie .
Bromhexin BerlinChemie .
Bromhexin ratiopharm .
Bromhexine, Famel .
Bromhexinratiopharm .
Dur Elix .
DurElix .
Hustentabs ratiopharm .
Hustentabsratiopharm .
Hydrochloride, Bromhexine .
Monohydrochloride, Bromhexine .
NA 274 .
NA274 .
ct, bromhexin von .
von ct, bromhexin .
A mucolytic agent used in the treatment of respiratory disorders associated with viscid or excessive mucus. (From Martindale, The Extra Pharmacopoeia, 30th ed, p744) .
1.00
 
Sotalol .
Darob .
MJ-1999 .
Sotalol Hydrochloride .
Sotalol Monohydrochloride .
MJ 1999 .
MJ1999 .
An adrenergic beta-antagonist that is used in the treatment of life-threatening arrhythmias. .
0.80
331992
 
Dichlorphenamide .
Daranide .
Dichlofenamide .
Glauconide .
Diclofenamid .
A carbonic anhydrase inhibitor that is used in the treatment of glaucoma. .
0.60
096
 
Dextropropoxyphene .
Darvon .
Propoxyphene .
Propoxyphene Hydrochloride .
Propoxyphene Hydrochloride, (R*,R*)-(+-)-Isomer .
Propoxyphene Hydrochloride, (R-(R*,R*))-Isomer .
Propoxyphene Hydrochloride, (R-(R*,S*))-Isomer .
Propoxyphene Hydrochloride, (S-(R*,R*))-Isomer .
Propoxyphene Maleate, (+)-Isomer .
Propoxyphene Phosphate, (S-(R*,S*))-Isomer .
Propoxyphene Sulfate, (S-(R*,S*))-Isomer .
D Propoxyphene .
Hydrochloride, Propoxyphene .
D-Propoxyphene .
Propoxyphene .
A narcotic analgesic structurally related to METHADONE. Only the dextro-isomer has an analgesic effect; the levo-isomer appears to exert an antitussive effect. .
0.60
241334
 
Pyrimethamine .
Chloridin .
Daraprim .
Malocide .
Tindurine .
One of the FOLIC ACID ANTAGONISTS that is used as an antimalarial or with a sulfonamide to treat toxoplasmosis. .
0.57
944143
 
Darkness .
Darknesses .
The absence of light. .
0.54
2511908
 
Darunavir .
Darunavir Ethanolate .
Prezista .
TMC 114 .
TMC-114 .
TMC114 .
UIC-94017 .
UIC94017 .
114, TMC .
Ethanolate, Darunavir .
UIC 94017 .
An HIV PROTEASE INHIBITOR that is used in the treatment of AIDS and HIV INFECTIONS. Due to the emergence of ANTIVIRAL DRUG RESISTANCE when used alone, it is administered in combination with other ANTI-HIV AGENTS. .
0.52
11688
 
Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 .
Dardarin Protein .
LRRK2 Protein .
PARK8 Protein .
Leucine Rich Repeat Serine Threonine Protein Kinase 2 .
A serine/threonine protein kinase with GTPase activity that contains 12 LEUCINE-rich repeats in its central region and 7 WD repeats C-terminal to its kinase and GTPase domains. It localizes to TRANSPORT VESICLES; the OUTER MITOCHONDRIAL MEMBRANE; and the GOLGI APPARATUS. It functions in PROTEIN TRANSPORT; regulates neuron morphology in the central nervous system, and also functions in the trafficking of SYNAPTIC VESICLES. Mutations in the LRRK2 gene have been identified in autosomal dominant cases of PARKINSON DISEASE (PARK8). .
0.51
01228
 
Darier Disease .
Acantholytic Dyskeratotic Epidermal Nevi .
Acantholytic Dyskeratotic Epidermal Nevus .
Acrokeratosis Verruciformis .
Darier's Disease .
Hopf Disease .
Darier White Disease .
Darier-White Diseases .
Dariers Disease .
Disease, Darier .
Disease, Darier's .
Disease, Darier-White .
Disease, Hopf .
Diseases, Darier-White .
Diseases, Hopf .
Hopf Acrokeratosis Verruciformis .
Hopf Diseases .
Verruciformis, Acrokeratosis .
Acrokeratosis Verruciformis of Hopf .
Darier-White Disease .
Keratosis Follicularis .
Darier's Disease .
An autosomal dominantly inherited skin disorder characterized by warty malodorous papules that coalesce into plaques. It is caused by mutations in the ATP2A2 gene encoding SERCA2 protein, one of the SARCOPLASMIC RETICULUM CALCIUM-TRANSPORTING ATPASES. The condition is similar, clinically and histologically, to BENIGN FAMILIAL PEMPHIGUS, another autosomal dominant skin disorder. Both diseases have defective calcium pumps (CALCIUM-TRANSPORTING ATPASES) and unstable desmosomal adhesion junctions (DESMOSOMES) between KERATINOCYTES. .
0.50
811424