serw-MX  [xml]  
 


    
 DeCS Categories

C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.595 Lysosomal Storage Diseases .
C16.320.565.595.377 Cystinosis .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.595 Lysosomal Storage Diseases .
C18.452.648.595.377 Cystinosis .
D02 Organic Chemicals .
D02.092 Amines .
D02.092.471 Ethylamines .
D02.092.471.200 Cystamine .
D02.522 Ketones .
D02.522.296 Butanones .
D02.522.296.400 Diacetyl .
D12 Amino Acids, Peptides, and Proteins .
D12.776 Proteins .
D12.776.215 Cystatins .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Cystamine .
2,2'-Dithiobisethanamine .
Cystamine Calcium Salt .
Cystamine Diacetate .
Cystamine Dihydrobromide .
Cystamine Dihydrochloride .
Cystamine Hydrobromide .
Cystamine Hydrochloride .
Cystamine Sulfate .
Cystamine Sulfate (1:1) .
Cysteinamine Disulfide .
Cystinamin .
2,2' Dithiobisethanamine .
Calcium Salt, Cystamine .
Diacetate, Cystamine .
Dihydrobromide, Cystamine .
Dihydrochloride, Cystamine .
Disulfide, Cysteinamine .
Hydrobromide, Cystamine .
Hydrochloride, Cystamine .
Sulfate, Cystamine .
Cystineamine .
Decarboxycystine .
Diaminodiethyldisulfide .
A radiation-protective agent that interferes with sulfhydryl enzymes. It may also protect against carbon tetrachloride liver damage. .
1.00
21046
 
Cystinosis .
Cystine Diathesis .
Cystine Disease .
Cystine Storage Disease .
Cystinoses .
Cystinosin, Defect of .
Cystinosis, Nephropathic .
Lysosomal Cystine Transport Protein, Defect Of .
Nephropathic Cystinosis .
Cystine Diatheses .
Cystine Diseases .
Cystine Storage Diseases .
Cystinoses, Nephropathic .
Defect of Cystinosin .
Defect of Cystinosins .
Diatheses, Cystine .
Diathesis, Cystine .
Nephropathic Cystinoses .
Storage Disease, Cystine .
Storage Diseases, Cystine .
A metabolic disease characterized by the defective transport of CYSTINE across the lysosomal membrane due to mutation of a membrane protein cystinosin. This results in cystine accumulation and crystallization in the cells causing widespread tissue damage. In the KIDNEY, nephropathic cystinosis is a common cause of RENAL FANCONI SYNDROME. .
0.60
131029
 
Cystatins .
Cystatin-Related Proteins .
Stefins .
Type 1 Cystatins .
Type 2 Cystatins .
Type 3 Cystatins .
Type I Cystatins .
Type II Cystatins .
Type III Cystatins .
Cystatin Related Proteins .
Cystatins, Type 1 .
Cystatins, Type 2 .
Cystatins, Type 3 .
Cystatins, Type I .
Cystatins, Type II .
Cystatins, Type III .
Cystatin Superfamily .
A homologous group of endogenous CYSTEINE PROTEINASE INHIBITORS. The cystatins inhibit most CYSTEINE ENDOPEPTIDASES such as PAPAIN, and other peptidases which have a sulfhydryl group at the active site. .
0.53
182578
 
Diacetyl .
2,3 Butanedione .
2,3-Butanedione .
Biacetyl .
Diketobutane .
Dimethyldiketone .
Dimethylglyoxal .
Carrier of aroma of butter, vinegar, coffee, and other foods. .
0.52
41174