serw-MX  [xml]  
 


    
 DeCS Categories

C14 Cardiovascular Diseases .
C14.240 Cardiovascular Abnormalities .
C14.240.400 Heart Defects, Congenital .
C14.240.400.172 Barth Syndrome .
C14.280 Heart Diseases .
C14.280.400 Heart Defects, Congenital .
C14.280.400.172 Barth Syndrome .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.131 Congenital Abnormalities .
C16.131.077 Abnormalities, Multiple .
C16.131.077.121 Barth Syndrome .
C16.131.240 Cardiovascular Abnormalities .
C16.131.240.400 Heart Defects, Congenital .
C16.131.240.400.172 Barth Syndrome .
C16.320 Genetic Diseases, Inborn .
C16.320.322 Genetic Diseases, X-Linked .
C16.320.322.068 Barth Syndrome .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.398 Lipid Metabolism, Inborn Errors .
C16.320.565.398.224 Barth Syndrome .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.398 Lipid Metabolism, Inborn Errors .
C18.452.648.398.224 Barth Syndrome .
D03 Heterocyclic Compounds .
D03.633 Heterocyclic Compounds, Fused-Ring .
D03.633.100 Heterocyclic Compounds, 2-Ring .
D03.633.100.759 Purines .
D03.633.100.759.646 Purine Nucleotides .
D03.633.100.759.646.138 Adenine Nucleotides .
D03.633.100.759.646.138.124 Adenosine Diphosphate .
D03.633.100.759.646.138.236 Adenosine Triphosphate .
D13 Nucleic Acids, Nucleotides, and Nucleosides .
D13.695 Nucleotides .
D13.695.667 Purine Nucleotides .
D13.695.667.138 Adenine Nucleotides .
D13.695.667.138.124 Adenosine Diphosphate .
D13.695.667.138.236 Adenosine Triphosphate .
D13.695.827 Ribonucleotides .
D13.695.827.068 Adenine Nucleotides .
D13.695.827.068.124 Adenosine Diphosphate .
D13.695.827.068.236 Adenosine Triphosphate .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Adenosine Diphosphate .
Adenosine 5'-Pyrophosphate .
5'-Pyrophosphate, Adenosine .
ADP, Magnesium .
Adenosine 5' Pyrophosphate .
Diphosphate, Adenosine .
Pyrophosphate, Adenosine .
Adenosine Pyrophosphate .
ADP 199 .
Magnesium ADP .
MgADP .
Adenosine 5'-(trihydrogen diphosphate). An adenine nucleotide containing two phosphate groups esterified to the sugar moiety at the 5'-position. .
1.00
3622549
 
Adenosine Triphosphate .
ATP-MgCl2 .
Adenosine Triphosphate, Chromium Ammonium Salt .
Adenosine Triphosphate, Magnesium Chloride .
Atriphos .
Chromium Adenosine Triphosphate .
Cr(H2O)4 ATP .
Magnesium Adenosine Triphosphate .
Striadyne .
ATP MgCl2 .
Adenosine Triphosphate, Calcium Salt .
Adenosine Triphosphate, Chromium Salt .
Adenosine Triphosphate, Magnesium Salt .
Adenosine Triphosphate, Manganese Salt .
Adenylpyrophosphate .
ATP 206 .
CaATP .
CrATP .
Manganese Adenosine Triphosphate .
MgATP .
MnATP .
MAGNESIUM ATP .
CALCIUM ATP .
CHROMIUM ATP .
An adenine nucleotide containing three phosphate groups esterified to the sugar moiety. In addition to its crucial roles in metabolism adenosine triphosphate is a neurotransmitter. .
0.74
13694772
 
Barth Syndrome .
3-Methylglutaconic Aciduria, Type II .
3-Methylglutaconicaciduria Type 2 .
3-Methylglutaconicaciduria Type II .
Cardioskeletal Myopathy with Neutropenia and Abnormal Mitochondria .
MGA Type 2 .
MGA Type II .
3 Methylglutaconic Aciduria, Type II .
3 Methylglutaconicaciduria Type 2 .
3-Methylglutaconicaciduria Type 2s .
3-Methylglutaconicaciduria Type IIs .
MGA Type 2s .
MGA Type IIs .
Syndrome, Barth .
Type 2, 3-Methylglutaconicaciduria .
Type 2, MGA .
Type 2s, MGA .
Type II, MGA .
Type IIs, MGA .
MGA type II .
3-methylglutaconicaciduria type 2 .
3-methylglutaconicaciduria type II .
Rare congenital X-linked disorder of lipid metabolism. Barth syndrome is transmitted in an X-linked recessive pattern. The syndrome is characterized by muscular weakness, growth retardation, DILATED CARDIOMYOPATHY, variable NEUTROPENIA, 3-methylglutaconic aciduria (type II) and decreases in mitochondrial CARDIOLIPIN level. Other biochemical and morphological mitochondrial abnormalities also exist. .
0.56
190