MeSH Treeview
Query OMIM entry list
256000
LS
LEIGH SYNDROME
→
High-scoring List
Musculoskeletal Diseases
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
MELAS Syndrome
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Muscle Weakness
Digestive System Diseases
Liver Diseases
Fatty Liver
Hepatic Insufficiency
Liver Failure
Respiratory Tract Diseases
Respiration Disorders
Hyperventilation
Alkalosis, Respiratory
Respiratory Insufficiency
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Canavan Disease
Leigh Disease
MELAS Syndrome
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Mitochondrial Encephalomyopathies
Wernicke Encephalopathy
Cerebrovascular Disorders
Cerebral Small Vessel Diseases
MELAS Syndrome
Stroke
Encephalitis
Encephalomyelitis
Encephalomalacia
Epilepsy
Epilepsies, Myoclonic
Epilepsy, Generalized
Spasms, Infantile
Seizures
Status Epilepticus
Epilepsia Partialis Continua
Leukoencephalopathies
Hereditary Central Nervous System Demyelinating Diseases
Canavan Disease
Central Nervous System Infections
Encephalomyelitis
Encephalomyelitis
Leukoencephalopathies
Hereditary Central Nervous System Demyelinating Diseases
Canavan Disease
Movement Disorders
Spinal Cord Diseases
Cranial Nerve Diseases
Ocular Motility Disorders
Ophthalmoplegia
Ophthalmoplegia, Chronic Progressive External
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Optic Nerve Diseases
Optic Atrophy
Demyelinating Diseases
Hereditary Central Nervous System Demyelinating Diseases
Canavan Disease
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Canavan Disease
Hereditary Central Nervous System Demyelinating Diseases
Neurologic Manifestations
Dyskinesias
Ataxia
Dystonia
Neurobehavioral Manifestations
Intellectual Disability
Mental Retardation, X-Linked
Pyruvate Dehydrogenase Complex Deficiency Disease
Psychomotor Disorders
Neuromuscular Manifestations
Muscle Hypotonia
Muscle Weakness
Paralysis
Ophthalmoplegia
Ophthalmoplegia, Chronic Progressive External
Paresis
Paraparesis
Paraparesis, Spastic
Seizures
Neuromuscular Diseases
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
MELAS Syndrome
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Eye Diseases
Eye Diseases, Hereditary
Retinitis Pigmentosa
Ocular Motility Disorders
Ophthalmoplegia
Ophthalmoplegia, Chronic Progressive External
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Optic Nerve Diseases
Optic Atrophy
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Kearns-Sayre Syndrome
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Fanconi Syndrome
Renal Tubular Transport, Inborn Errors
Fanconi Syndrome
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Fanconi Syndrome
Renal Tubular Transport, Inborn Errors
Fanconi Syndrome
Pregnancy Complications
Fetal Death
Cardiovascular Diseases
Heart Diseases
Arrhythmias, Cardiac
Pre-Excitation Syndromes
Wolff-Parkinson-White Syndrome
Cardiomyopathies
Cardiomyopathy, Hypertrophic
Kearns-Sayre Syndrome
Heart Valve Diseases
Aortic Valve Stenosis
Aortic Stenosis, Subvalvular
Cardiomyopathy, Hypertrophic
Vascular Diseases
Cerebrovascular Disorders
Cerebral Small Vessel Diseases
MELAS Syndrome
Stroke
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Cardiovascular Abnormalities
Heart Defects, Congenital
Wolff-Parkinson-White Syndrome
Chromosome Disorders
Genetic Diseases, Inborn
Chromosome Disorders
Eye Diseases, Hereditary
Retinitis Pigmentosa
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Pyruvate Dehydrogenase Complex Deficiency Disease
Heredodegenerative Disorders, Nervous System
Canavan Disease
Hereditary Central Nervous System Demyelinating Diseases
Mental Retardation, X-Linked
Pyruvate Dehydrogenase Complex Deficiency Disease
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Canavan Disease
Leigh Disease
MELAS Syndrome
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Carbohydrate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
Leigh Disease
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Cytochrome-c Oxidase Deficiency
Renal Tubular Transport, Inborn Errors
Fanconi Syndrome
Infant, Newborn, Diseases
Nutritional and Metabolic Diseases
Metabolic Diseases
Acid-Base Imbalance
Acidosis
Acidosis, Lactic
Alkalosis
Alkalosis, Respiratory
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Canavan Disease
Leigh Disease
MELAS Syndrome
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Mitochondrial Encephalomyopathies
Wernicke Encephalopathy
Glucose Metabolism Disorders
Diabetes Mellitus
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Canavan Disease
Leigh Disease
MELAS Syndrome
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Carbohydrate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
Leigh Disease
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Renal Tubular Transport, Inborn Errors
Fanconi Syndrome
Mitochondrial Diseases
Cytochrome-c Oxidase Deficiency
Kearns-Sayre Syndrome
Leigh Disease
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
MELAS Syndrome
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Nutrition Disorders
Malnutrition
Deficiency Diseases
Avitaminosis
Vitamin B Deficiency
Thiamine Deficiency
Wernicke Encephalopathy
Endocrine System Diseases
Diabetes Mellitus
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Nondisjunction, Genetic
Uniparental Disomy
Death
Death, Sudden
Sudden Infant Death
Fetal Death
Disease
Syndrome
Disease Attributes
Recurrence
Muscle Weakness
Necrosis
Signs and Symptoms
Failure to Thrive
Neurologic Manifestations
Dyskinesias
Ataxia
Dystonia
Neurobehavioral Manifestations
Intellectual Disability
Psychomotor Disorders
Neuromuscular Manifestations
Muscle Hypotonia
Muscle Weakness
Paralysis
Ophthalmoplegia
Ophthalmoplegia, Chronic Progressive External
Paresis
Paraparesis
Paraparesis, Spastic
Seizures
Signs and Symptoms, Respiratory
Hyperventilation
Hypocapnia
Substance-Related Disorders
Alcohol-Related Disorders
Wernicke Encephalopathy
Database Center for Life Science
