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516060
MTATP6
ATP SYNTHASE 6
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Musculoskeletal Diseases
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
Muscle Weakness
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Leigh Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Mitochondrial Encephalomyopathies
Cerebellar Diseases
Spinocerebellar Degenerations
Epilepsy
Epilepsies, Myoclonic
Myoclonic Epilepsies, Progressive
Ocular Motility Disorders
Spinal Cord Diseases
Spinocerebellar Degenerations
Cranial Nerve Diseases
Ocular Motility Disorders
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Optic Atrophies, Hereditary
Spinocerebellar Degenerations
Neurologic Manifestations
Dyskinesias
Ataxia
Gait Ataxia
Gait Disorders, Neurologic
Gait Ataxia
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Articulation Disorders
Dysarthria
Intellectual Disability
Mental Retardation, X-Linked
Pyruvate Dehydrogenase Complex Deficiency Disease
Neuromuscular Manifestations
Muscle Hypotonia
Muscle Weakness
Paresis
Neuromuscular Diseases
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Eye Diseases
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Retinitis Pigmentosa
Ocular Motility Disorders
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Fetal Death
Fetal Diseases
Cardiovascular Diseases
Heart Diseases
Cardiomyopathies
Cardiomyopathy, Hypertrophic
Heart Valve Diseases
Aortic Valve Stenosis
Aortic Stenosis, Subvalvular
Cardiomyopathy, Hypertrophic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Fetal Diseases
Genetic Diseases, Inborn
Chromosome Disorders
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Retinitis Pigmentosa
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Pyruvate Dehydrogenase Complex Deficiency Disease
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Mental Retardation, X-Linked
Pyruvate Dehydrogenase Complex Deficiency Disease
Optic Atrophies, Hereditary
Spinocerebellar Degenerations
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Leigh Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Carbohydrate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
Leigh Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Nutritional and Metabolic Diseases
Metabolic Diseases
Acid-Base Imbalance
Acidosis
Acidosis, Lactic
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Leigh Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Mitochondrial Encephalomyopathies
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Leigh Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Carbohydrate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
Leigh Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Mitochondrial Diseases
Leigh Disease
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
Pyruvate Dehydrogenase Complex Deficiency Disease
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Death
Death, Sudden
Sudden Infant Death
Fetal Death
Disease
Syndrome
Disease Attributes
Recurrence
Muscle Weakness
Necrosis
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Gait Ataxia
Gait Disorders, Neurologic
Gait Ataxia
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Articulation Disorders
Dysarthria
Intellectual Disability
Neuromuscular Manifestations
Muscle Hypotonia
Muscle Weakness
Paresis
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