Leukodystrophy, Metachromatic

"Leukodystrophy, Metachromatic" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

An autosomal recessive metabolic disease caused by a deficiency of CEREBROSIDE-SULFATASE leading to intralysosomal accumulation of cerebroside sulfate (SULFOGLYCOSPHINGOLIPIDS) in the nervous system and other organs. Pathological features include diffuse demyelination, and metachromatically-staining granules in many cell types such as the GLIAL CELLS. There are several allelic and nonallelic forms with a variety of neurological symptoms.

Descriptor ID	D007966
MeSH Number(s)	C10.228.140.163.100.362.550 C10.228.140.163.100.435.825.850.500 C10.228.140.695.625.550 C10.314.400.550 C16.320.565.189.362.550 C16.320.565.189.435.825.850.500 C16.320.565.398.641.803.925.500 C16.320.565.595.554.825.850.500 C18.452.132.100.362.550 C18.452.132.100.435.825.850.500 C18.452.584.687.803.925.500 C18.452.648.189.362.550 C18.452.648.189.435.825.850.500 C18.452.648.398.641.803.925.500 C18.452.648.595.554.825.850.500
Concept/Terms	Leukodystrophy, Metachromatic Leukodystrophy, Metachromatic Leukodystrophies, Metachromatic Metachromatic Leukodystrophies Cerebral sclerosis, Diffuse, Metachromatic Form Sulfatide Lipidosis Lipidosis, Sulfatide Metachromatic Leukodystrophy Metachromatic Leukoencephalopathy Leukoencephalopathies, Metachromatic Leukoencephalopathy, Metachromatic Metachromatic Leukoencephalopathies Arylsulfatase A Deficiency Disease Cerebroside Sulphatase Deficiency Disease Leukodystrophy, Metachromatic, Adult Leukodystrophy, Metachromatic, Adult Metachromatic Leukodystrophy, Adult-Type Adult-Type Metachromatic Leukodystrophies Adult-Type Metachromatic Leukodystrophy Leukodystrophies, Adult-Type Metachromatic Leukodystrophy, Adult-Type Metachromatic Metachromatic Leukodystrophies, Adult-Type Metachromatic Leukodystrophy, Adult Type Metachromatic Leukodystrophy, Adult Adult Metachromatic Leukodystrophies Adult Metachromatic Leukodystrophy Leukodystrophies, Adult Metachromatic Leukodystrophy, Adult Metachromatic Metachromatic Leukodystrophies, Adult Metachromatic Leukodystrophy, Infant Metachromatic Leukodystrophy, Infant Infant Metachromatic Leukodystrophies Infant Metachromatic Leukodystrophy Metachromatic Leukodystrophies, Infant Metachromatic Leukodystrophy, Late Infantile Greenfield's Disease Greenfield Disease Metachromatic Leukodystrophy, Infant-Type Infant-Type Metachromatic Leukodystrophies Infant-Type Metachromatic Leukodystrophy Metachromatic Leukodystrophies, Infant-Type Metachromatic Leukodystrophy, Infant Type Arylsulfatase A Deficiency Arylsulfatase A Deficiency Arylsulfatase A Deficiencies Deficiencies, Arylsulfatase A Deficiency, Arylsulfatase A ARSA Deficiency ARSA Deficiencies Deficiencies, ARSA Deficiency, ARSA Cerebroside Sulfatase Deficiency Cerebroside Sulfatase Deficiencies Deficiencies, Cerebroside Sulfatase Deficiency, Cerebroside Sulfatase Sulfatase Deficiencies, Cerebroside Sulfatase Deficiency, Cerebroside Leukodystrophy, Metachromatic, Juvenile Leukodystrophy, Metachromatic, Juvenile Metachromatic Leukodystrophy, Juvenile-Type Juvenile-Type Metachromatic Leukodystrophies Juvenile-Type Metachromatic Leukodystrophy Leukodystrophies, Juvenile-Type Metachromatic Leukodystrophy, Juvenile-Type Metachromatic Metachromatic Leukodystrophies, Juvenile-Type Metachromatic Leukodystrophy, Juvenile Type Metachromatic Leukodystrophy, Juvenile Juvenile Metachromatic Leukodystrophies Juvenile Metachromatic Leukodystrophy Leukodystrophies, Juvenile Metachromatic Leukodystrophy, Juvenile Metachromatic Metachromatic Leukodystrophies, Juvenile

Below are MeSH descriptors whose meaning is more general than "Leukodystrophy, Metachromatic".

Diseases [C]
Nervous System Diseases [C10]
Central Nervous System Diseases [C10.228]
Brain Diseases [C10.228.140]
Brain Diseases, Metabolic [C10.228.140.163]
Brain Diseases, Metabolic, Inborn [C10.228.140.163.100]
Hereditary Central Nervous System Demyelinating Diseases [C10.228.140.163.100.362]
Leukodystrophy, Metachromatic [C10.228.140.163.100.362.550]
Lysosomal Storage Diseases, Nervous System [C10.228.140.163.100.435]
Sphingolipidoses [C10.228.140.163.100.435.825]
Sulfatidosis [C10.228.140.163.100.435.825.850]
Leukodystrophy, Metachromatic [C10.228.140.163.100.435.825.850.500]
Leukoencephalopathies [C10.228.140.695]
Hereditary Central Nervous System Demyelinating Diseases [C10.228.140.695.625]
Leukodystrophy, Metachromatic [C10.228.140.695.625.550]
Demyelinating Diseases [C10.314]
Hereditary Central Nervous System Demyelinating Diseases [C10.314.400]
Leukodystrophy, Metachromatic [C10.314.400.550]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Metabolism, Inborn Errors [C16.320.565]
Brain Diseases, Metabolic, Inborn [C16.320.565.189]
Hereditary Central Nervous System Demyelinating Diseases [C16.320.565.189.362]
Leukodystrophy, Metachromatic [C16.320.565.189.362.550]
Lysosomal Storage Diseases, Nervous System [C16.320.565.189.435]
Sphingolipidoses [C16.320.565.189.435.825]
Sulfatidosis [C16.320.565.189.435.825.850]
Leukodystrophy, Metachromatic [C16.320.565.189.435.825.850.500]
Lipid Metabolism, Inborn Errors [C16.320.565.398]
Lipidoses [C16.320.565.398.641]
Sphingolipidoses [C16.320.565.398.641.803]
Sulfatidosis [C16.320.565.398.641.803.925]
Leukodystrophy, Metachromatic [C16.320.565.398.641.803.925.500]
Lysosomal Storage Diseases [C16.320.565.595]
Lysosomal Storage Diseases, Nervous System [C16.320.565.595.554]
Sphingolipidoses [C16.320.565.595.554.825]
Sulfatidosis [C16.320.565.595.554.825.850]
Leukodystrophy, Metachromatic [C16.320.565.595.554.825.850.500]
Nutritional and Metabolic Diseases [C18]
Metabolic Diseases [C18.452]
Brain Diseases, Metabolic [C18.452.132]
Brain Diseases, Metabolic, Inborn [C18.452.132.100]
Hereditary Central Nervous System Demyelinating Diseases [C18.452.132.100.362]
Leukodystrophy, Metachromatic [C18.452.132.100.362.550]
Lysosomal Storage Diseases, Nervous System [C18.452.132.100.435]
Sphingolipidoses [C18.452.132.100.435.825]
Sulfatidosis [C18.452.132.100.435.825.850]
Leukodystrophy, Metachromatic [C18.452.132.100.435.825.850.500]
Lipid Metabolism Disorders [C18.452.584]
Lipidoses [C18.452.584.687]
Sphingolipidoses [C18.452.584.687.803]
Sulfatidosis [C18.452.584.687.803.925]
Leukodystrophy, Metachromatic [C18.452.584.687.803.925.500]
Metabolism, Inborn Errors [C18.452.648]
Brain Diseases, Metabolic, Inborn [C18.452.648.189]
Hereditary Central Nervous System Demyelinating Diseases [C18.452.648.189.362]
Leukodystrophy, Metachromatic [C18.452.648.189.362.550]
Lysosomal Storage Diseases, Nervous System [C18.452.648.189.435]
Sphingolipidoses [C18.452.648.189.435.825]
Sulfatidosis [C18.452.648.189.435.825.850]
Leukodystrophy, Metachromatic [C18.452.648.189.435.825.850.500]
Lipid Metabolism, Inborn Errors [C18.452.648.398]
Lipidoses [C18.452.648.398.641]
Sphingolipidoses [C18.452.648.398.641.803]
Sulfatidosis [C18.452.648.398.641.803.925]
Leukodystrophy, Metachromatic [C18.452.648.398.641.803.925.500]
Lysosomal Storage Diseases [C18.452.648.595]
Lysosomal Storage Diseases, Nervous System [C18.452.648.595.554]
Sphingolipidoses [C18.452.648.595.554.825]
Sulfatidosis [C18.452.648.595.554.825.850]
Leukodystrophy, Metachromatic [C18.452.648.595.554.825.850.500]

Below are MeSH descriptors whose meaning is related to "Leukodystrophy, Metachromatic".

Below are MeSH descriptors whose meaning is more specific than "Leukodystrophy, Metachromatic".

publications

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