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220110
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MITOCHONDRIAL COMPLEX IV DEFICIENCY
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Musculoskeletal Diseases
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
Rhabdomyolysis
Myoglobinuria
Digestive System Diseases
Liver Diseases
Hepatic Insufficiency
Liver Failure
Hepatic Encephalopathy
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Deafness
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Leigh Disease
Hepatic Encephalopathy
Mitochondrial Encephalomyopathies
Encephalomalacia
Epilepsy
Epilepsies, Myoclonic
Epilepsy, Generalized
Spasms, Infantile
Spinal Cord Diseases
Muscular Atrophy, Spinal
Spinal Muscular Atrophies of Childhood
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Spinal Muscular Atrophies of Childhood
Motor Neuron Disease
Muscular Atrophy, Spinal
Spinal Muscular Atrophies of Childhood
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Psychomotor Disorders
Neuromuscular Manifestations
Muscle Hypotonia
Paresis
Paraparesis
Paraparesis, Spastic
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Neuromuscular Diseases
Motor Neuron Disease
Muscular Atrophy, Spinal
Spinal Muscular Atrophies of Childhood
Muscular Atrophy, Spinal
Spinal Muscular Atrophies of Childhood
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Fanconi Syndrome
Renal Tubular Transport, Inborn Errors
Acidosis, Renal Tubular
Fanconi Syndrome
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Fanconi Syndrome
Renal Tubular Transport, Inborn Errors
Acidosis, Renal Tubular
Fanconi Syndrome
Pregnancy Complications
Fetal Diseases
Fetal Growth Retardation
Cardiovascular Diseases
Heart Diseases
Cardiomegaly
Cardiomyopathies
Cardiomyopathy, Hypertrophic
Heart Valve Diseases
Aortic Valve Stenosis
Aortic Stenosis, Subvalvular
Cardiomyopathy, Hypertrophic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Fetal Diseases
Fetal Growth Retardation
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Spinal Muscular Atrophies of Childhood
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Leigh Disease
Carbohydrate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
Leigh Disease
Cytochrome-c Oxidase Deficiency
Renal Tubular Transport, Inborn Errors
Acidosis, Renal Tubular
Fanconi Syndrome
Infant, Newborn, Diseases
Nutritional and Metabolic Diseases
Metabolic Diseases
Acid-Base Imbalance
Acidosis
Acidosis, Lactic
Acidosis, Renal Tubular
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Leigh Disease
Hepatic Encephalopathy
Mitochondrial Encephalomyopathies
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Leigh Disease
Carbohydrate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
Leigh Disease
Renal Tubular Transport, Inborn Errors
Acidosis, Renal Tubular
Fanconi Syndrome
Mitochondrial Diseases
Cytochrome-c Oxidase Deficiency
Leigh Disease
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Hypertrophy
Cardiomegaly
Pathologic Processes
Disease
Syndrome
Disease Attributes
Recurrence
Growth Disorders
Fetal Growth Retardation
Nerve Degeneration
Shock
Multiple Organ Failure
Signs and Symptoms
Failure to Thrive
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Psychomotor Disorders
Neuromuscular Manifestations
Muscle Hypotonia
Paresis
Paraparesis
Paraparesis, Spastic
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
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