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Query OMIM entry list
609560
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MITOCHONDRIAL DNA DEPLETION SYNDROME, MYOPATHIC FORM
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Musculoskeletal Diseases
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
Digestive System Diseases
Liver Diseases
Fatty Liver
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Mitochondrial Encephalomyopathies
Spinal Cord Diseases
Muscular Atrophy, Spinal
Cranial Nerve Diseases
Ocular Motility Disorders
Ophthalmoplegia
Neurodegenerative Diseases
Motor Neuron Disease
Muscular Atrophy, Spinal
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Hypotonia
Paralysis
Ophthalmoplegia
Neuromuscular Diseases
Motor Neuron Disease
Muscular Atrophy, Spinal
Muscular Atrophy, Spinal
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
Eye Diseases
Ocular Motility Disorders
Ophthalmoplegia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Cytochrome-c Oxidase Deficiency
Nutritional and Metabolic Diseases
Metabolic Diseases
Acid-Base Imbalance
Acidosis
Brain Diseases, Metabolic
Mitochondrial Encephalomyopathies
Metabolism, Inborn Errors
Mitochondrial Diseases
Cytochrome-c Oxidase Deficiency
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Disease
Syndrome
Disease Attributes
Disease Progression
Signs and Symptoms
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Hypotonia
Paralysis
Ophthalmoplegia
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