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248600
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MAPLE SYRUP URINE DISEASE
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Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Galactosemias
Leigh Disease
Maple Syrup Urine Disease
Phenylketonurias
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Cerebellar Diseases
Spinocerebellar Degenerations
Friedreich Ataxia
Epilepsy
Seizures
Spinal Cord Diseases
Spinocerebellar Degenerations
Friedreich Ataxia
Cranial Nerve Diseases
Ocular Motility Disorders
Ophthalmoplegia
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Spinocerebellar Degenerations
Friedreich Ataxia
Neurologic Manifestations
Dyskinesias
Ataxia
Hyperkinesis
Neurobehavioral Manifestations
Consciousness Disorders
Unconsciousness
Intellectual Disability
Mental Retardation, X-Linked
Pyruvate Dehydrogenase Complex Deficiency Disease
Paralysis
Ophthalmoplegia
Seizures
Eye Diseases
Ocular Motility Disorders
Ophthalmoplegia
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Fetal Diseases
Fetal Growth Retardation
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Macrocytic
Anemia, Megaloblastic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Fetal Diseases
Fetal Growth Retardation
Genetic Diseases, Inborn
Chromosome Disorders
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Pyruvate Dehydrogenase Complex Deficiency Disease
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Pyruvate Dehydrogenase Complex Deficiency Disease
Spinocerebellar Degenerations
Friedreich Ataxia
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Maple Syrup Urine Disease
Phenylketonurias
Brain Diseases, Metabolic, Inborn
Galactosemias
Leigh Disease
Maple Syrup Urine Disease
Phenylketonurias
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Carbohydrate Metabolism, Inborn Errors
Galactosemias
Pyruvate Metabolism, Inborn Errors
Leigh Disease
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Infant, Newborn, Diseases
Nutritional and Metabolic Diseases
Metabolic Diseases
Acid-Base Imbalance
Acidosis
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Galactosemias
Leigh Disease
Maple Syrup Urine Disease
Phenylketonurias
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Maple Syrup Urine Disease
Phenylketonurias
Brain Diseases, Metabolic, Inborn
Galactosemias
Leigh Disease
Maple Syrup Urine Disease
Phenylketonurias
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Carbohydrate Metabolism, Inborn Errors
Galactosemias
Pyruvate Metabolism, Inborn Errors
Leigh Disease
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Mitochondrial Diseases
Friedreich Ataxia
Leigh Disease
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Growth Disorders
Fetal Growth Retardation
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Hyperkinesis
Neurobehavioral Manifestations
Consciousness Disorders
Unconsciousness
Intellectual Disability
Paralysis
Ophthalmoplegia
Seizures
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