Concept information
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Metabolism, Inborn Errors
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
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Metabolism, Inborn Errors
Lysosomal Storage Diseases
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
...
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
...
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
...
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Lysosomal Storage Diseases, Nervous System
Sphingolipidoses
Preferred term
Niemann-Pick Diseases
Type
-
Topical Descriptor
Broader concept
Narrower concepts
Entry terms
- Niemann Pick Disease
- Niemann-Pick Disease
Note
- note specific types are available
Scope note
- A group of autosomal recessive disorders in which harmful quantities of lipids accumulate in the viscera and the central nervous system. They can be caused by deficiencies of enzyme activities (SPHINGOMYELIN PHOSPHODIESTERASE) or defects in intracellular transport, resulting in the accumulation of SPHINGOMYELINS and CHOLESTEROL. There are various subtypes based on their clinical and genetic differences.
History note
- 2000(1966)
In other languages
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Finnish
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morbus Niemann-Pick
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Niemann-Pick
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Niemann-Pickin tauti
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sfingomyeliinilipidoosi
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sfingomyeliinilipidoosit
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Swedish
URI
http://www.yso.fi/onto/mesh/D009542
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