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233910
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GTP CYCLOHYDROLASE I DEFICIENCY
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Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Phenylketonurias
Neurologic Manifestations
Dyskinesias
Dystonia
Neuromuscular Manifestations
Muscle Hypotonia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Phenylketonurias
Brain Diseases, Metabolic, Inborn
Phenylketonurias
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Phenylketonurias
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Phenylketonurias
Brain Diseases, Metabolic, Inborn
Phenylketonurias
Pathological Conditions, Signs and Symptoms
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Dystonia
Neuromuscular Manifestations
Muscle Hypotonia
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