Descriptor English: | Leukodystrophy, Metachromatic | ||||||
Descriptor Spanish: |
Leucodistrofia Metacromática
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Descriptor Portuguese: | Leucodistrofia Metacromática | ||||||
Descriptor French: | Leucodystrophie métachromatique | ||||||
Entry term(s): |
ARSA Deficiencies ARSA Deficiency Adult Metachromatic Leukodystrophies Adult Metachromatic Leukodystrophy Adult-Type Metachromatic Leukodystrophies Adult-Type Metachromatic Leukodystrophy Arylsulfatase A Deficiencies Arylsulfatase A Deficiency Arylsulfatase A Deficiency Disease Cerebral sclerosis, Diffuse, Metachromatic Form Cerebroside Sulfatase Deficiencies Cerebroside Sulfatase Deficiency Cerebroside Sulphatase Deficiency Disease Deficiencies, ARSA Deficiencies, Arylsulfatase A Deficiencies, Cerebroside Sulfatase Deficiency, ARSA Deficiency, Arylsulfatase A Deficiency, Cerebroside Sulfatase Greenfield Disease Greenfield's Disease Infant Metachromatic Leukodystrophies Infant Metachromatic Leukodystrophy Infant-Type Metachromatic Leukodystrophies Infant-Type Metachromatic Leukodystrophy Juvenile Metachromatic Leukodystrophies Juvenile Metachromatic Leukodystrophy Juvenile-Type Metachromatic Leukodystrophies Juvenile-Type Metachromatic Leukodystrophy Leukodystrophies, Adult Metachromatic Leukodystrophies, Adult-Type Metachromatic Leukodystrophies, Juvenile Metachromatic Leukodystrophies, Juvenile-Type Metachromatic Leukodystrophies, Metachromatic Leukodystrophy, Adult Metachromatic Leukodystrophy, Adult-Type Metachromatic Leukodystrophy, Juvenile Metachromatic Leukodystrophy, Juvenile-Type Metachromatic Leukodystrophy, Metachromatic, Adult Leukodystrophy, Metachromatic, Juvenile Leukoencephalopathies, Metachromatic Leukoencephalopathy, Metachromatic Lipidosis, Sulfatide Metachromatic Leukodystrophies Metachromatic Leukodystrophies, Adult Metachromatic Leukodystrophies, Adult-Type Metachromatic Leukodystrophies, Infant Metachromatic Leukodystrophies, Infant-Type Metachromatic Leukodystrophies, Juvenile Metachromatic Leukodystrophies, Juvenile-Type Metachromatic Leukodystrophy Metachromatic Leukodystrophy, Adult Metachromatic Leukodystrophy, Adult Type Metachromatic Leukodystrophy, Adult-Type Metachromatic Leukodystrophy, Infant Metachromatic Leukodystrophy, Infant Type Metachromatic Leukodystrophy, Infant-Type Metachromatic Leukodystrophy, Juvenile Metachromatic Leukodystrophy, Juvenile Type Metachromatic Leukodystrophy, Juvenile-Type Metachromatic Leukodystrophy, Late Infantile Metachromatic Leukoencephalopathies Metachromatic Leukoencephalopathy Sulfatase Deficiencies, Cerebroside Sulfatase Deficiency, Cerebroside Sulfatide Lipidosis |
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Tree 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 C18.452.584.563.641.803.925.500 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 |
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RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D007966 | ||||||
Scope note: | 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. |
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Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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Public MeSH Note: | 1974 |
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History Note: | 1974 |
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Related: |
Cerebroside-Sulfatase
MeSH | ||||||
DeCS ID: | 8143 | ||||||
Unique ID: | D007966 | ||||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
Date Established: | 1974/01/01 | ||||||
Date of Entry: | 1999/01/01 | ||||||
Revision Date: | 2013/07/08 |
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Leukodystrophy, Metachromatic
- Preferred
Leukodystrophy, Metachromatic, Adult
- Narrower
Metachromatic Leukodystrophy, Infant
- Narrower
Arylsulfatase A Deficiency
- Narrower
Leukodystrophy, Metachromatic, Juvenile
- Narrower
Concept UI |
M0012416 |
Scope note | 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. |
Preferred term | Leukodystrophy, Metachromatic |
Entry term(s) |
Arylsulfatase A Deficiency Disease Cerebral sclerosis, Diffuse, Metachromatic Form Cerebroside Sulphatase Deficiency Disease Leukodystrophies, Metachromatic Leukoencephalopathies, Metachromatic Leukoencephalopathy, Metachromatic Lipidosis, Sulfatide Metachromatic Leukodystrophies Metachromatic Leukodystrophy Metachromatic Leukoencephalopathies Metachromatic Leukoencephalopathy Sulfatide Lipidosis |
Concept UI |
M0335513 |
Preferred term | Leukodystrophy, Metachromatic, Adult |
Entry term(s) |
Adult Metachromatic Leukodystrophies Adult Metachromatic Leukodystrophy Adult-Type Metachromatic Leukodystrophies Adult-Type Metachromatic Leukodystrophy Leukodystrophies, Adult Metachromatic Leukodystrophies, Adult-Type Metachromatic Leukodystrophy, Adult Metachromatic Leukodystrophy, Adult-Type Metachromatic Metachromatic Leukodystrophies, Adult Metachromatic Leukodystrophies, Adult-Type Metachromatic Leukodystrophy, Adult Metachromatic Leukodystrophy, Adult Type Metachromatic Leukodystrophy, Adult-Type |
Concept UI |
M0335515 |
Preferred term | Metachromatic Leukodystrophy, Infant |
Entry term(s) |
Greenfield Disease Greenfield's Disease Infant Metachromatic Leukodystrophies Infant Metachromatic Leukodystrophy Infant-Type Metachromatic Leukodystrophies Infant-Type Metachromatic Leukodystrophy Metachromatic Leukodystrophies, Infant Metachromatic Leukodystrophies, Infant-Type Metachromatic Leukodystrophy, Infant Type Metachromatic Leukodystrophy, Infant-Type Metachromatic Leukodystrophy, Late Infantile |
Concept UI |
M0535751 |
Preferred term | Arylsulfatase A Deficiency |
Entry term(s) |
ARSA Deficiencies ARSA Deficiency Arylsulfatase A Deficiencies Cerebroside Sulfatase Deficiencies Cerebroside Sulfatase Deficiency Deficiencies, ARSA Deficiencies, Arylsulfatase A Deficiencies, Cerebroside Sulfatase Deficiency, ARSA Deficiency, Arylsulfatase A Deficiency, Cerebroside Sulfatase Sulfatase Deficiencies, Cerebroside Sulfatase Deficiency, Cerebroside |
Concept UI |
M0335514 |
Preferred term | Leukodystrophy, Metachromatic, Juvenile |
Entry term(s) |
Juvenile Metachromatic Leukodystrophies Juvenile Metachromatic Leukodystrophy Juvenile-Type Metachromatic Leukodystrophies Juvenile-Type Metachromatic Leukodystrophy Leukodystrophies, Juvenile Metachromatic Leukodystrophies, Juvenile-Type Metachromatic Leukodystrophy, Juvenile Metachromatic Leukodystrophy, Juvenile-Type Metachromatic Metachromatic Leukodystrophies, Juvenile Metachromatic Leukodystrophies, Juvenile-Type Metachromatic Leukodystrophy, Juvenile Metachromatic Leukodystrophy, Juvenile Type Metachromatic Leukodystrophy, Juvenile-Type |
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