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516050
MTCO3
CYTOCHROME c OXIDASE III
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Musculoskeletal Diseases
Muscular Diseases
Mitochondrial Myopathies
Rhabdomyolysis
Myoglobinuria
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Leigh Disease
Cranial Nerve Diseases
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Optic Atrophies, Hereditary
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Paresis
Paraparesis
Paraparesis, Spastic
Neuromuscular Diseases
Muscular Diseases
Mitochondrial Myopathies
Eye Diseases
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Heredodegenerative Disorders, Nervous System
Optic Atrophies, Hereditary
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Leigh Disease
Carbohydrate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
Leigh Disease
Cytochrome-c Oxidase Deficiency
Nutritional and Metabolic Diseases
Metabolic Diseases
Acid-Base Imbalance
Acidosis
Acidosis, Lactic
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Leigh Disease
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Leigh Disease
Carbohydrate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
Leigh Disease
Mitochondrial Diseases
Cytochrome-c Oxidase Deficiency
Leigh Disease
Mitochondrial Myopathies
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Disease Attributes
Recurrence
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Paresis
Paraparesis
Paraparesis, Spastic
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