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Query OMIM entry list
590050
MTTL1
TRANSFER RNA, MITOCHONDRIAL, LEUCINE, 1
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Musculoskeletal Diseases
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
MELAS Syndrome
MERRF Syndrome
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Muscle Weakness
Musculoskeletal Abnormalities
Limb Deformities, Congenital
Digestive System Diseases
Digestive System Abnormalities
Anus, Imperforate
Digestive System Fistula
Esophageal Fistula
Tracheoesophageal Fistula
Gastrointestinal Diseases
Esophageal Diseases
Esophageal Fistula
Tracheoesophageal Fistula
Respiratory Tract Diseases
Respiratory Tract Fistula
Tracheoesophageal Fistula
Tracheal Diseases
Tracheoesophageal Fistula
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Deafness
Hearing Loss, Sensorineural
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
MELAS Syndrome
MERRF Syndrome
Pyruvate Dehydrogenase Complex Deficiency Disease
Mitochondrial Encephalomyopathies
Cerebellar Diseases
Cerebellar Ataxia
Cerebrovascular Disorders
Cerebral Small Vessel Diseases
MELAS Syndrome
Dementia
Encephalitis
Encephalomyelitis
Epilepsy
Epilepsies, Myoclonic
Myoclonic Epilepsies, Progressive
MERRF Syndrome
Seizures
Headache Disorders
Headache Disorders, Primary
Migraine Disorders
Hypothalamic Diseases
Central Nervous System Infections
Encephalomyelitis
Encephalomyelitis
Cranial Nerve Diseases
Ocular Motility Disorders
Ophthalmoplegia
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Optic Atrophies, Hereditary
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Neurobehavioral Manifestations
Communication Disorders
Learning Disorders
Intellectual Disability
Mental Retardation, X-Linked
Pyruvate Dehydrogenase Complex Deficiency Disease
Psychomotor Disorders
Neuromuscular Manifestations
Muscle Weakness
Pain
Paralysis
Ophthalmoplegia
Seizures
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Hearing Loss, Sensorineural
Neuromuscular Diseases
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
MELAS Syndrome
MERRF Syndrome
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Eye Diseases
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Retinitis Pigmentosa
Lens Diseases
Cataract
Ocular Motility Disorders
Ophthalmoplegia
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Retinal Diseases
Retinal Degeneration
Macular Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Kearns-Sayre Syndrome
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Nephritis
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Nephritis
Pregnancy Complications
Diabetes, Gestational
Obstetric Labor Complications
Placenta Accreta
Placenta Diseases
Placenta Accreta
Pregnancy in Diabetics
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Heart Diseases
Arrhythmias, Cardiac
Pre-Excitation Syndromes
Wolff-Parkinson-White Syndrome
Cardiomegaly
Cardiomyopathy, Dilated
Cardiomyopathies
Cardiomyopathy, Dilated
Cardiomyopathy, Hypertrophic
Kearns-Sayre Syndrome
Heart Defects, Congenital
Heart Valve Diseases
Aortic Valve Stenosis
Aortic Stenosis, Subvalvular
Cardiomyopathy, Hypertrophic
Vascular Diseases
Cerebrovascular Disorders
Cerebral Small Vessel Diseases
MELAS Syndrome
Hemic and Lymphatic Diseases
Hematologic Diseases
Bone Marrow Diseases
Myelodysplastic Syndromes
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Cardiovascular Abnormalities
Heart Defects, Congenital
Wolff-Parkinson-White Syndrome
Digestive System Abnormalities
Anus, Imperforate
Musculoskeletal Abnormalities
Limb Deformities, Congenital
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Optic Atrophies, Hereditary
Retinitis Pigmentosa
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
MELAS Syndrome
MERRF Syndrome
Pyruvate Dehydrogenase Complex Deficiency Disease
Carbohydrate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
Pyruvate Dehydrogenase Complex Deficiency Disease
Cytochrome-c Oxidase Deficiency
Nutritional and Metabolic Diseases
Metabolic Diseases
Acid-Base Imbalance
Acidosis
Acidosis, Lactic
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
MELAS Syndrome
MERRF Syndrome
Pyruvate Dehydrogenase Complex Deficiency Disease
Mitochondrial Encephalomyopathies
Calcium Metabolism Disorders
Calcinosis
Glucose Metabolism Disorders
Diabetes Mellitus
Diabetes Mellitus, Type 1
Diabetes Mellitus, Type 2
Diabetes, Gestational
Hyperglycemia
Glucose Intolerance
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
MELAS Syndrome
MERRF Syndrome
Pyruvate Dehydrogenase Complex Deficiency Disease
Carbohydrate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
Pyruvate Dehydrogenase Complex Deficiency Disease
Mitochondrial Diseases
Cytochrome-c Oxidase Deficiency
Kearns-Sayre Syndrome
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 Complications
Diabetes, Gestational
Diabetes Mellitus, Type 1
Diabetes Mellitus, Type 2
Gonadal Disorders
Hypogonadism
Thyroid Diseases
Hyperthyroidism
Immune System Diseases
Autoimmune Diseases
Diabetes Mellitus, Type 1
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Fistula
Digestive System Fistula
Esophageal Fistula
Tracheoesophageal Fistula
Pathologic Processes
Death
Death, Sudden
Sudden Infant Death
Disease
Syndrome
Disease Attributes
Disease Progression
Recurrence
Muscle Weakness
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Neurobehavioral Manifestations
Communication Disorders
Learning Disorders
Psychomotor Disorders
Neuromuscular Manifestations
Muscle Weakness
Pain
Paralysis
Ophthalmoplegia
Seizures
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Hearing Loss, Sensorineural
Pain
Signs and Symptoms, Digestive
Vomiting
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