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Query OMIM entry list
590060
MTTK
TRANSFER RNA, MITOCHONDRIAL, LYSINE
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Musculoskeletal Diseases
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
MELAS Syndrome
MERRF Syndrome
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Digestive System Diseases
Gastrointestinal Diseases
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Deafness
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Parkinsonian Disorders
Parkinson Disease
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Leigh Disease
MELAS Syndrome
MERRF Syndrome
Pyruvate Dehydrogenase Complex Deficiency Disease
Mitochondrial Encephalomyopathies
Cerebrovascular Disorders
Cerebral Small Vessel Diseases
MELAS Syndrome
Epilepsy
Epilepsies, Myoclonic
Myoclonic Epilepsies, Progressive
MERRF Syndrome
Movement Disorders
Parkinsonian Disorders
Parkinson Disease
Cranial Nerve Diseases
Ocular Motility Disorders
Ophthalmoplegia
Ophthalmoplegia, Chronic Progressive External
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Optic Atrophies, Hereditary
Parkinson Disease
Neurologic Manifestations
Dyskinesias
Ataxia
Neurobehavioral Manifestations
Intellectual Disability
Mental Retardation, X-Linked
Pyruvate Dehydrogenase Complex Deficiency Disease
Paralysis
Ophthalmoplegia
Ophthalmoplegia, Chronic Progressive External
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Neuromuscular Diseases
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
MELAS Syndrome
MERRF Syndrome
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Peripheral Nervous System Diseases
Eye Diseases
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Ocular Motility Disorders
Ophthalmoplegia
Ophthalmoplegia, Chronic Progressive External
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Kearns-Sayre Syndrome
Cardiovascular Diseases
Heart Diseases
Cardiomegaly
Cardiomyopathy, Dilated
Cardiomyopathies
Cardiomyopathy, Dilated
Kearns-Sayre Syndrome
Vascular Diseases
Cerebrovascular Disorders
Cerebral Small Vessel Diseases
MELAS Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Genetic Diseases, Inborn
Chromosome Disorders
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Pyruvate Dehydrogenase Complex Deficiency Disease
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Pyruvate Dehydrogenase Complex Deficiency Disease
Optic Atrophies, Hereditary
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Leigh Disease
MELAS Syndrome
MERRF Syndrome
Pyruvate Dehydrogenase Complex Deficiency Disease
Carbohydrate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
Leigh Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Nutritional and Metabolic Diseases
Metabolic Diseases
Acid-Base Imbalance
Acidosis
Acidosis, Lactic
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Leigh Disease
MELAS Syndrome
MERRF Syndrome
Pyruvate Dehydrogenase Complex Deficiency Disease
Mitochondrial Encephalomyopathies
Glucose Metabolism Disorders
Diabetes Mellitus
Diabetes Mellitus, Type 1
Diabetes Mellitus, Type 2
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Leigh Disease
MELAS Syndrome
MERRF Syndrome
Pyruvate Dehydrogenase Complex Deficiency Disease
Carbohydrate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
Leigh Disease
Pyruvate Dehydrogenase Complex Deficiency Disease
Mitochondrial Diseases
Kearns-Sayre Syndrome
Leigh Disease
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
MELAS Syndrome
MERRF Syndrome
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Pyruvate Dehydrogenase Complex Deficiency Disease
Endocrine System Diseases
Diabetes Mellitus
Diabetes Mellitus, Type 1
Diabetes Mellitus, Type 2
Immune System Diseases
Autoimmune Diseases
Diabetes Mellitus, Type 1
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Disease
Syndrome
Disease Attributes
Disease Progression
Diseases in Twins
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Paralysis
Ophthalmoplegia
Ophthalmoplegia, Chronic Progressive External
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
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