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Query OMIM entry list
220111
LSFC
LEIGH SYNDROME, FRENCH-CANADIAN TYPE
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Musculoskeletal Diseases
Muscular Diseases
Digestive System Diseases
Liver Diseases
Fatty Liver
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Leigh Disease
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Hypotonia
Neuromuscular Diseases
Muscular Diseases
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
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
Pathological Conditions, Signs and Symptoms
Signs and Symptoms
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Hypotonia
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