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607574
ARSA
ARYLSULFATASE A
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Musculoskeletal Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Myotonic Dystrophy
Myotonic Disorders
Myotonic Dystrophy
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Leukoencephalopathies
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Leukoencephalopathies
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Demyelinating Diseases
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Myotonic Dystrophy
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Learning Disorders
Intellectual Disability
Mental Retardation, X-Linked
Fragile X Syndrome
Neuromuscular Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Myotonic Dystrophy
Myotonic Disorders
Myotonic Dystrophy
Peripheral Nervous System Diseases
Polyneuropathies
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Chromosome Disorders
Sex Chromosome Disorders
Fragile X Syndrome
Genetic Diseases, Inborn
Chromosome Disorders
Sex Chromosome Disorders
Fragile X Syndrome
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Fragile X Syndrome
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Fragile X Syndrome
Myotonic Dystrophy
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Lipid Metabolism, Inborn Errors
Lipidoses
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Muscular Dystrophies
Myotonic Dystrophy
Nutritional and Metabolic Diseases
Metabolic Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Lipid Metabolism Disorders
Lipidoses
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Lipid Metabolism, Inborn Errors
Lipidoses
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Sulfatidosis
Leukodystrophy, Metachromatic
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Ring Chromosomes
Translocation, Genetic
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Learning Disorders
Database Center for Life Science
