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261630
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PHENYLKETONURIA II
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Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Huntington Disease
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Phenylketonurias
Dementia
Huntington Disease
Epilepsy
Seizures
Movement Disorders
Dyskinesias
Chorea
Huntington Disease
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Huntington Disease
Neurologic Manifestations
Dyskinesias
Dystonia
Seizures
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Huntington Disease
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
Calcium Metabolism Disorders
Calcinosis
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Phenylketonurias
Brain Diseases, Metabolic, Inborn
Phenylketonurias
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Disease Attributes
Disease Progression
Diseases in Twins
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Dystonia
Seizures
Database Center for Life Science
