MeSH Treeview
Query OMIM entry list
608307
CPS1
CARBAMOYL PHOSPHATE SYNTHETASE I
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Respiratory Tract Diseases
Lung Diseases
Hypertension, Pulmonary
Persistent Fetal Circulation Syndrome
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Urea Cycle Disorders, Inborn
Carbamoyl-Phosphate Synthase I Deficiency Disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Urea Cycle Disorders, Inborn
Carbamoyl-Phosphate Synthase I Deficiency Disease
Brain Diseases, Metabolic, Inborn
Urea Cycle Disorders, Inborn
Carbamoyl-Phosphate Synthase I Deficiency Disease
Infant, Newborn, Diseases
Persistent Fetal Circulation Syndrome
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Urea Cycle Disorders, Inborn
Carbamoyl-Phosphate Synthase I Deficiency Disease
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Urea Cycle Disorders, Inborn
Carbamoyl-Phosphate Synthase I Deficiency Disease
Brain Diseases, Metabolic, Inborn
Urea Cycle Disorders, Inborn
Carbamoyl-Phosphate Synthase I Deficiency Disease
Mitochondrial Diseases
Carbamoyl-Phosphate Synthase I Deficiency Disease
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Hyperammonemia
Database Center for Life Science
