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300257
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DANON DISEASE
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Musculoskeletal Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Muscular Dystrophy, Emery-Dreifuss
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Glycogen Storage Disease Type II
Sphingolipidoses
Fabry Disease
Cerebrovascular Disorders
Cerebral Small Vessel Diseases
Fabry Disease
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Mental Retardation, X-Linked
Glycogen Storage Disease Type IIb
Neuromuscular Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Muscular Dystrophy, Emery-Dreifuss
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Eye Diseases
Eye Diseases, Hereditary
Retinitis Pigmentosa
Lens Diseases
Cataract
Refractive Errors
Myopia
Retinal Diseases
Retinal Degeneration
Macular Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Cardiovascular Diseases
Heart Diseases
Arrhythmias, Cardiac
Heart Block
Cardiomegaly
Cardiomyopathy, Dilated
Hypertrophy, Left Ventricular
Cardiomyopathies
Cardiomyopathy, Dilated
Cardiomyopathy, Hypertrophic
Cardiomyopathy, Hypertrophic, Familial
Glycogen Storage Disease Type IIb
Heart Valve Diseases
Aortic Valve Stenosis
Aortic Stenosis, Subvalvular
Cardiomyopathy, Hypertrophic
Vascular Diseases
Cerebrovascular Disorders
Cerebral Small Vessel Diseases
Fabry Disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Genetic Diseases, Inborn
Cardiomyopathy, Hypertrophic, Familial
Eye Diseases, Hereditary
Retinitis Pigmentosa
Genetic Diseases, X-Linked
Fabry Disease
Glycogen Storage Disease Type IIb
Muscular Dystrophy, Emery-Dreifuss
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Glycogen Storage Disease Type II
Sphingolipidoses
Fabry Disease
Carbohydrate Metabolism, Inborn Errors
Glycogen Storage Disease
Glycogen Storage Disease Type II
Glycogen Storage Disease Type IIb
Lipid Metabolism, Inborn Errors
Lipidoses
Sphingolipidoses
Fabry Disease
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Glycogen Storage Disease Type II
Sphingolipidoses
Fabry Disease
Muscular Dystrophies
Muscular Dystrophy, Emery-Dreifuss
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Glycogen Storage Disease Type II
Sphingolipidoses
Fabry Disease
Lipid Metabolism Disorders
Lipidoses
Sphingolipidoses
Fabry Disease
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Glycogen Storage Disease Type II
Sphingolipidoses
Fabry Disease
Carbohydrate Metabolism, Inborn Errors
Glycogen Storage Disease
Glycogen Storage Disease Type II
Glycogen Storage Disease Type IIb
Lipid Metabolism, Inborn Errors
Lipidoses
Sphingolipidoses
Fabry Disease
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Glycogen Storage Disease Type II
Sphingolipidoses
Fabry Disease
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Hypertrophy
Cardiomegaly
Hypertrophy, Left Ventricular
Pathologic Processes
Arrhythmias, Cardiac
Heart Block
Disease
Syndrome
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
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