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250100
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METACHROMATIC LEUKODYSTROPHY
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Neoplasms
Neoplasms by Site
Nervous System Neoplasms
Central Nervous System Neoplasms
Central Nervous System Cysts
Musculoskeletal Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Nervous System Diseases
Autoimmune Diseases of the Nervous System
Demyelinating Autoimmune Diseases, CNS
Diffuse Cerebral Sclerosis of Schilder
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Dystonia Musculorum Deformans
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Fabry Disease
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Niemann-Pick Diseases
Sulfatidosis
Leukodystrophy, Metachromatic
Cerebrovascular Disorders
Cerebral Small Vessel Diseases
Fabry Disease
Dementia, Vascular
Intracranial Arterial Diseases
Intracranial Arteriosclerosis
Dementia, Vascular
Dementia
Dementia, Vascular
Diffuse Cerebral Sclerosis of Schilder
Leukoencephalopathies
Dementia, Vascular
Demyelinating Autoimmune Diseases, CNS
Diffuse Cerebral Sclerosis of Schilder
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Leukoencephalopathies
Dementia, Vascular
Demyelinating Autoimmune Diseases, CNS
Diffuse Cerebral Sclerosis of Schilder
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Movement Disorders
Dystonic Disorders
Dystonia Musculorum Deformans
Cranial Nerve Diseases
Optic Nerve Diseases
Optic Atrophy
Demyelinating Diseases
Demyelinating Autoimmune Diseases, CNS
Diffuse Cerebral Sclerosis of Schilder
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Nervous System Malformations
Central Nervous System Cysts
Nervous System Neoplasms
Central Nervous System Neoplasms
Central Nervous System Cysts
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Dystonia Musculorum Deformans
Neurologic Manifestations
Dyskinesias
Dystonia
Neurobehavioral Manifestations
Catatonia
Communication Disorders
Language Disorders
Speech Disorders
Articulation Disorders
Dysarthria
Intellectual Disability
Psychomotor Disorders
Sensation Disorders
Vision Disorders
Blindness
Neuromuscular Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Peripheral Nervous System Diseases
Eye Diseases
Optic Nerve Diseases
Optic Atrophy
Vision Disorders
Blindness
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Fetal Diseases
Cardiovascular Diseases
Vascular Diseases
Arterial Occlusive Diseases
Arteriosclerosis
Intracranial Arteriosclerosis
Dementia, Vascular
Cerebrovascular Disorders
Cerebral Small Vessel Diseases
Fabry Disease
Intracranial Arterial Diseases
Intracranial Arteriosclerosis
Dementia, Vascular
Hemic and Lymphatic Diseases
Lymphatic Diseases
Histiocytosis
Histiocytosis, Non-Langerhans-Cell
Niemann-Pick Diseases
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Nervous System Malformations
Central Nervous System Cysts
Fetal Diseases
Genetic Diseases, Inborn
Chromosome Disorders
Genetic Diseases, X-Linked
Fabry Disease
Heredodegenerative Disorders, Nervous System
Dystonia Musculorum Deformans
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Fabry Disease
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Niemann-Pick Diseases
Sulfatidosis
Leukodystrophy, Metachromatic
Carbohydrate Metabolism, Inborn Errors
Glycogen Storage Disease
Mucopolysaccharidoses
Mucopolysaccharidosis I
Mucopolysaccharidosis VI
Lipid Metabolism, Inborn Errors
Lipidoses
Sphingolipidoses
Fabry Disease
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Niemann-Pick Diseases
Sulfatidosis
Leukodystrophy, Metachromatic
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Fabry Disease
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Niemann-Pick Diseases
Sulfatidosis
Leukodystrophy, Metachromatic
Mucopolysaccharidoses
Mucopolysaccharidosis I
Mucopolysaccharidosis VI
Muscular Dystrophies
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Mucinoses
Mucopolysaccharidoses
Mucopolysaccharidosis I
Mucopolysaccharidosis VI
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
Fabry Disease
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Niemann-Pick Diseases
Sulfatidosis
Leukodystrophy, Metachromatic
Lipid Metabolism Disorders
Lipid Metabolism, Inborn Errors
Lipidoses
Sphingolipidoses
Fabry Disease
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Niemann-Pick Diseases
Sulfatidosis
Leukodystrophy, Metachromatic
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Hereditary Central Nervous System Demyelinating Diseases
Leukodystrophy, Metachromatic
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Fabry Disease
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Niemann-Pick Diseases
Sulfatidosis
Leukodystrophy, Metachromatic
Carbohydrate Metabolism, Inborn Errors
Glycogen Storage Disease
Mucopolysaccharidoses
Mucopolysaccharidosis I
Mucopolysaccharidosis VI
Lipid Metabolism, Inborn Errors
Lipidoses
Sphingolipidoses
Fabry Disease
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Niemann-Pick Diseases
Sulfatidosis
Leukodystrophy, Metachromatic
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Fabry Disease
Gangliosidoses
Gangliosidoses, GM2
Tay-Sachs Disease
Niemann-Pick Diseases
Sulfatidosis
Leukodystrophy, Metachromatic
Mucopolysaccharidoses
Mucopolysaccharidosis I
Mucopolysaccharidosis VI
Immune System Diseases
Autoimmune Diseases
Autoimmune Diseases of the Nervous System
Demyelinating Autoimmune Diseases, CNS
Diffuse Cerebral Sclerosis of Schilder
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Disease Attributes
Disease Progression
Disease Susceptibility
Genetic Predisposition to Disease
Diseases in Twins
Signs and Symptoms
Neurologic Manifestations
Dyskinesias
Dystonia
Neurobehavioral Manifestations
Catatonia
Communication Disorders
Language Disorders
Speech Disorders
Articulation Disorders
Dysarthria
Intellectual Disability
Psychomotor Disorders
Sensation Disorders
Vision Disorders
Blindness
Database Center for Life Science
