Urea cycle defects. Medical search. Frequent questions

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Diseases9

Urea Cycle Disorders, Inborn Hyperammonemia Hyperargininemia Ornithine Carbamoyltransferase Deficiency Disease Argininosuccinic Aciduria Metabolism, Inborn Errors Carbamoyl-Phosphate Synthase I Deficiency Disease Citrullinemia Amino Acid Metabolism, Inborn Errors

Chemicals and Drugs17

Urea Argininosuccinate Synthase Carbamoyl-Phosphate Synthase (Ammonia)Argininosuccinate Lyase Ornithine Carbamoyltransferase Argininosuccinic Acid Amino-Acid N-Acetyltransferase Arginase Cell Cycle Proteins Ammonia Ornithine Sodium Benzoate Phenylbutyrates Orotic Acid Citrulline Carbamyl Phosphate Arginine

Phenomena and Processes2

Cell Cycle Mutation

Diseases Chemicals and Drugs Phenomena and Processes

Urea Cycle Disorders, Inborn Hyperammonemia Urea Cell Cycle Argininosuccinate Synthase Carbamoyl-Phosphate Synthase (Ammonia)Argininosuccinate Lyase Hyperargininemia Ornithine Carbamoyltransferase Ornithine Carbamoyltransferase Deficiency Disease Argininosuccinic Acid Amino-Acid N-Acetyltransferase Argininosuccinic Aciduria Arginase Cell Cycle Proteins Mutation Ammonia Metabolism, Inborn Errors Ornithine Carbamoyl-Phosphate Synthase I Deficiency Disease Sodium Benzoate Citrullinemia Phenylbutyrates Orotic Acid Citrulline Amino Acid Metabolism, Inborn Errors Carbamyl Phosphate Arginine

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