MeSH Treeview
Query OMIM entry list
229300
FRDA
FRIEDREICH ATAXIA 1
→
High-scoring List
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Osteochondrodysplasias
Osteogenesis Imperfecta
Spinal Diseases
Spinal Curvatures
Scoliosis
Muscular Diseases
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
Muscular Disorders, Atrophic
Muscular Dystrophies
Muscular Dystrophy, Duchenne
Myotonic Dystrophy
Myotonic Disorders
Myotonic Dystrophy
Respiratory Tract Diseases
Lung Diseases
Pneumonia
Respiratory Tract Infections
Pneumonia
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Deafness
Nervous System Diseases
Autoimmune Diseases of the Nervous System
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Autonomic Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Huntington Disease
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Pyruvate Dehydrogenase Complex Deficiency Disease
Mitochondrial Encephalomyopathies
Cerebellar Diseases
Cerebellar Ataxia
Spinocerebellar Ataxias
Spinocerebellar Degenerations
Friedreich Ataxia
Spinocerebellar Ataxias
Dementia
Huntington Disease
Epilepsy
Epilepsies, Partial
Epilepsy, Generalized
Epilepsy, Tonic-Clonic
Movement Disorders
Dyskinesias
Chorea
Huntington Disease
Ocular Motility Disorders
Spinal Cord Diseases
Muscular Atrophy, Spinal
Spinocerebellar Degenerations
Friedreich Ataxia
Spinocerebellar Ataxias
Cranial Nerve Diseases
Ocular Motility Disorders
Nystagmus, Pathologic
Optic Nerve Diseases
Optic Atrophy
Demyelinating Diseases
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Nervous System Malformations
Hereditary Sensory and Autonomic Neuropathies
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Autonomic Neuropathies
Huntington Disease
Myotonic Dystrophy
Spinocerebellar Degenerations
Friedreich Ataxia
Spinocerebellar Ataxias
Motor Neuron Disease
Muscular Atrophy, Spinal
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Spinocerebellar Ataxias
Gait Ataxia
Chorea
Myoclonus
Gait Disorders, Neurologic
Gait Ataxia
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Intellectual Disability
Mental Retardation, X-Linked
Fragile X Syndrome
Pyruvate Dehydrogenase Complex Deficiency Disease
Psychomotor Disorders
Apraxias
Paralysis
Quadriplegia
Reflex, Abnormal
Reflex, Babinski
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Vision Disorders
Neuromuscular Diseases
Motor Neuron Disease
Muscular Atrophy, Spinal
Muscular Atrophy, Spinal
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Muscular Dystrophy, Duchenne
Myotonic Dystrophy
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
Myotonic Disorders
Myotonic Dystrophy
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Autonomic Neuropathies
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Eye Diseases
Ocular Motility Disorders
Nystagmus, Pathologic
Optic Nerve Diseases
Optic Atrophy
Vision Disorders
Male Urogenital Diseases
Urologic Diseases
Urinary Bladder Diseases
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Urinary Bladder Diseases
Pregnancy Complications
Fetal Death
Fetal Diseases
Cardiovascular Diseases
Heart Diseases
Arrhythmias, Cardiac
Tachycardia
Cardiomegaly
Cardiomyopathy, Dilated
Hypertrophy, Left Ventricular
Cardiomyopathies
Cardiomyopathy, Dilated
Cardiomyopathy, Hypertrophic
Heart Failure
Heart Valve Diseases
Aortic Valve Stenosis
Aortic Stenosis, Subvalvular
Cardiomyopathy, Hypertrophic
Myocardial Ischemia
Myocardial Infarction
Ventricular Dysfunction
Ventricular Dysfunction, Left
Ventricular Outflow Obstruction
Aortic Valve Stenosis
Vascular Diseases
Hypertension
Myocardial Ischemia
Myocardial Infarction
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Sex Chromosome Disorders
Fragile X Syndrome
Nervous System Malformations
Hereditary Sensory and Autonomic Neuropathies
Fetal Diseases
Genetic Diseases, Inborn
Chromosome Disorders
Sex Chromosome Disorders
Fragile X Syndrome
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Fragile X Syndrome
Pyruvate Dehydrogenase Complex Deficiency Disease
Muscular Dystrophy, Duchenne
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Autonomic Neuropathies
Huntington Disease
Mental Retardation, X-Linked
Fragile X Syndrome
Pyruvate Dehydrogenase Complex Deficiency Disease
Myotonic Dystrophy
Spinocerebellar Degenerations
Friedreich Ataxia
Spinocerebellar Ataxias
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Pyruvate Dehydrogenase Complex Deficiency Disease
Carbohydrate Metabolism, Inborn Errors
Mucopolysaccharidoses
Pyruvate Metabolism, Inborn Errors
Pyruvate Dehydrogenase Complex Deficiency Disease
Lysosomal Storage Diseases
Mucopolysaccharidoses
Muscular Dystrophies
Muscular Dystrophy, Duchenne
Myotonic Dystrophy
Osteogenesis Imperfecta
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Collagen Diseases
Osteogenesis Imperfecta
Mucinoses
Mucopolysaccharidoses
Nutritional and Metabolic Diseases
Metabolic Diseases
Acid-Base Imbalance
Acidosis
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Pyruvate Dehydrogenase Complex Deficiency Disease
Mitochondrial Encephalomyopathies
Glucose Metabolism Disorders
Diabetes Mellitus
Iron Metabolism Disorders
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Pyruvate Dehydrogenase Complex Deficiency Disease
Carbohydrate Metabolism, Inborn Errors
Mucopolysaccharidoses
Pyruvate Metabolism, Inborn Errors
Pyruvate Dehydrogenase Complex Deficiency Disease
Lysosomal Storage Diseases
Mucopolysaccharidoses
Mitochondrial Diseases
Friedreich Ataxia
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
Pyruvate Dehydrogenase Complex Deficiency Disease
Nutrition Disorders
Malnutrition
Deficiency Diseases
Avitaminosis
Vitamin E Deficiency
Endocrine System Diseases
Diabetes Mellitus
Diabetes Complications
Immune System Diseases
Autoimmune Diseases
Autoimmune Diseases of the Nervous System
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Hypertrophy
Cardiomegaly
Hypertrophy, Left Ventricular
Pathologic Processes
Arrhythmias, Cardiac
Tachycardia
Chromosome Aberrations
Chromosome Breakage
Chromosome Inversion
Death
Fetal Death
Disease Attributes
Disease Progression
Disease Susceptibility
Genetic Predisposition to Disease
Genomic Instability
Microsatellite Instability
Necrosis
Nerve Degeneration
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Gait Ataxia
Chorea
Myoclonus
Gait Disorders, Neurologic
Gait Ataxia
Neurobehavioral Manifestations
Apraxias
Communication Disorders
Language Disorders
Speech Disorders
Intellectual Disability
Psychomotor Disorders
Apraxias
Paralysis
Quadriplegia
Reflex, Abnormal
Reflex, Babinski
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Vision Disorders
Database Center for Life Science
