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 DeCS Categories

C04 Neoplasms .
C04.588 Neoplasms by Site .
C04.588.945 Urogenital Neoplasms .
C04.588.945.947 Urologic Neoplasms .
C04.588.945.947.940 Ureteral Neoplasms .
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 .
C10.228.140.163.100.937 Urea Cycle Disorders, Inborn .
C10.228.140.163.100.937.124 Argininosuccinic Aciduria .
C12 Male Urogenital Diseases .
C12.758 Urogenital Neoplasms .
C12.758.820 Urologic Neoplasms .
C12.758.820.875 Ureteral Neoplasms .
C12.777 Urologic Diseases .
C12.777.725 Ureteral Diseases .
C12.777.725.676 Ureteral Neoplasms .
C13 Female Urogenital Diseases and Pregnancy Complications .
C13.351 Female Urogenital Diseases .
C13.351.937 Urogenital Neoplasms .
C13.351.937.820 Urologic Neoplasms .
C13.351.937.820.875 Ureteral Neoplasms .
C13.351.968 Urologic Diseases .
C13.351.968.725 Ureteral Diseases .
C13.351.968.725.676 Ureteral Neoplasms .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.100 Amino Acid Metabolism, Inborn Errors .
C16.320.565.100.940 Urea Cycle Disorders, Inborn .
C16.320.565.100.940.124 Argininosuccinic Aciduria .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.937 Urea Cycle Disorders, Inborn .
C16.320.565.189.937.124 Argininosuccinic Aciduria .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.937 Urea Cycle Disorders, Inborn .
C18.452.132.100.937.124 Argininosuccinic Aciduria .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.100 Amino Acid Metabolism, Inborn Errors .
C18.452.648.100.940 Urea Cycle Disorders, Inborn .
C18.452.648.100.940.124 Argininosuccinic Aciduria .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.937 Urea Cycle Disorders, Inborn .
C18.452.648.189.937.124 Argininosuccinic Aciduria .
D02 Organic Chemicals .
D02.241 Carboxylic Acids .
D02.241.081 Acids, Acyclic .
D02.241.081.337 Dicarboxylic Acids .
D02.241.081.337.759 Succinates .
D02.241.081.337.759.124 Argininosuccinic Acid .
D08 Enzymes and Coenzymes .
D08.811 Enzymes .
D08.811.277 Hydrolases .
D08.811.277.087 Amidohydrolases .
D08.811.277.087.902 Urease .
D08.811.464 Ligases .
D08.811.464.259 Carbon-Nitrogen Ligases .
D08.811.464.259.300 Argininosuccinate Synthase .
D12 Amino Acids, Peptides, and Proteins .
D12.125 Amino Acids .
D12.125.068 Amino Acids, Basic .
D12.125.068.050 Arginine .
D12.125.068.050.075 Argininosuccinic Acid .
D12.125.068.665 Ornithine .
D12.125.095 Amino Acids, Diamino .
D12.125.095.104 Arginine .
D12.125.095.104.075 Argininosuccinic Acid .
D12.125.095.765 Ornithine .
 
 Terms
 Synonyms & Historicals
Documents
LILACS e MDL
 
Ornithine .
2,5-Diaminopentanoic Acid .
Ornithine Dihydrochloride, (L)-Isomer .
Ornithine Hydrochloride, (D)-Isomer .
Ornithine Hydrochloride, (DL)-Isomer .
Ornithine Hydrochloride, (L)-Isomer .
Ornithine Monoacetate, (L)-Isomer .
Ornithine Monohydrobromide, (L)-Isomer .
Ornithine Monohydrochloride, (D)-Isomer .
Ornithine Monohydrochloride, (DL)-Isomer .
Ornithine Phosphate (1:1), (L)-Isomer .
Ornithine Sulfate (1:1), (L)-Isomer .
Ornithine, (D)-Isomer .
Ornithine, (DL)-Isomer .
Ornithine, (L)-Isomer .
2,5 Diaminopentanoic Acid .
An amino acid produced in the urea cycle by the splitting off of urea from arginine. .
1.00
134465
 
Argininosuccinic Acid .
N-(4-Amino-4-carboxybutyl)amidino-L-aspartic Acid .
Acid, Argininosuccinic .
This amino acid is formed during the urea cycle from citrulline, aspartate and ATP. This reaction is catalyzed by argininosuccinic acid synthetase. .
0.40
2160
 
Argininosuccinic Aciduria .
ASA Deficiency .
ASL Deficiency .
Argininosuccinase Deficiency .
Argininosuccinate Acidemia .
Argininosuccinate Lyase Deficiency .
Argininosuccinic Acid Lyase Deficiency .
Argininosuccinic Acidemia .
Argininosuccinicaciduria .
Argininosuccinyl-Coa Lyase Deficiency .
Arginosuccinase Deficiency .
Asauria .
Inborn Error of Urea Synthesis, Arginino Succinic Type .
Urea Cycle Disorder, Arginino Succinase Type .
ASA Deficiencies .
ASL Deficiencies .
Acidemia, Argininosuccinate .
Acidemias, Argininosuccinate .
Aciduria, Argininosuccinic .
Acidurias, Argininosuccinic .
Arginino Succinase Deficiencies .
Argininosuccinate Acidemias .
Argininosuccinate Lyase Deficiencies .
Argininosuccinic Acidurias .
Argininosuccinicacidurias .
Deficiencies, ASA .
Deficiencies, ASL .
Deficiencies, Arginino Succinase .
Deficiencies, Argininosuccinate Lyase .
Deficiency, ASA .
Deficiency, ASL .
Deficiency, Arginino Succinase .
Deficiency, Argininosuccinate Lyase .
Arginino Succinase Deficiency .
Rare autosomal recessive disorder of the urea cycle which leads to the accumulation of argininosuccinic acid in body fluids and severe HYPERAMMONEMIA. Clinical features of the neonatal onset of the disorder include poor feeding, vomiting, lethargy, seizures, tachypnea, coma, and death. Later onset results in milder set of clinical features including vomiting, failure to thrive, irritability, behavioral problems, or psychomotor retardation. Mutations in the ARGININOSUCCINATE LYASE gene cause the disorder. .
0.37
0137
 
Urease .
Phytourease .
Urea Amidohydrolase .
Amidohydrolase, Urea .
An enzyme that catalyzes the conversion of urea and water to carbon dioxide and ammonia. EC 3.5.1.5. .
0.37
1224806
 
Urea Cycle Disorders, Inborn .
Disorder, Urea Cycle .
Disorders, Urea Cycle .
Urea Cycle Disorder .
Inborn Urea Cycle Disorder .
Urea Cycle Disorders .
Rare congenital metabolism disorders of the urea cycle. The disorders are due to mutations that result in complete (neonatal onset) or partial (childhood or adult onset) inactivity of an enzyme, involved in the urea cycle. Neonatal onset results in clinical features that include irritability, vomiting, lethargy, seizures, NEONATAL HYPOTONIA; RESPIRATORY ALKALOSIS; HYPERAMMONEMIA; coma, and death. Survivors of the neonatal onset and childhood/adult onset disorders share common risks for ENCEPHALOPATHIES, METABOLIC, INBORN; and RESPIRATORY ALKALOSIS due to HYPERAMMONEMIA. .
0.37
4188
 
Argininosuccinate Synthase .
Argininosuccinate Synthetase .
Synthase, Argininosuccinate .
Synthetase, Argininosuccinate .
An enzyme of the urea cycle that catalyzes the formation of argininosuccinic acid from citrulline and aspartic acid in the presence of ATP. Absence or deficiency of this enzyme causes the metabolic disease CITRULLINEMIA in humans. EC 6.3.4.5. .
0.35
1724
 
Ureteral Neoplasms .
Cancer of the Ureter .
Neoplasms of Ureter .
Neoplasms, Ureteral .
Ureter Cancer .
Ureter Neoplasms .
Ureter, Cancer Of .
Cancer, Ureteral .
Cancers, Ureteral .
Neoplasm, Ureteral .
Ureter Cancers .
Ureter Neoplasm .
Ureteral Cancers .
Ureteral Neoplasm .
Cancer of Ureter .
Ureteral Cancer .
Cancer or tumors of the URETER which may cause obstruction leading to hydroureter, HYDRONEPHROSIS, and PYELONEPHRITIS. HEMATURIA is a common symptom. .
0.35
503939