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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. .
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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. .
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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. .
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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. .
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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. .
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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. .
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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. .
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