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237300	-	CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY, HYPERAMMONEMIA DUE TO

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Digestive System Diseases

Nervous System Diseases

Central Nervous System Diseases

Brain Diseases, Metabolic

Brain Diseases, Metabolic, Inborn

Urea Cycle Disorders, Inborn

Carbamoyl-Phosphate Synthase I Deficiency Disease

Epilepsy, Generalized

Neurologic Manifestations

Neurobehavioral Manifestations

Consciousness Disorders

Unconsciousness

Neuromuscular Manifestations

Muscle Hypotonia

Female Urogenital Diseases and Pregnancy Complications

Pregnancy Complications

Puerperal Disorders

Hemic and Lymphatic Diseases

Hematologic Diseases

Blood Group Incompatibility

Erythroblastosis, Fetal

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

Erythroblastosis, Fetal

Skin and Connective Tissue Diseases

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

Immune System Diseases

Blood Group Incompatibility

Erythroblastosis, Fetal

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