 Niemann-Pick Disease, Type B
"Niemann-Pick Disease, Type B" 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.
An allelic disorder of TYPE A NIEMANN-PICK DISEASE, a late-onset form. It is also caused by mutation in SPHINGOMYELIN PHOSPHODIESTERASE but clinical signs involve only visceral organs (non-neuropathic type).
| Descriptor ID |
D052537
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| MeSH Number(s) |
C10.228.140.163.100.435.825.700.750 C15.604.250.410.625.750 C16.320.565.189.435.825.700.750 C16.320.565.398.641.803.730.750 C16.320.565.595.554.825.700.750 C18.452.132.100.435.825.700.750 C18.452.584.687.803.730.750 C18.452.648.189.435.825.700.750 C18.452.648.398.641.803.730.750 C18.452.648.595.554.825.700.750
|
| Concept/Terms |
Niemann-Pick Disease, Type B- Niemann-Pick Disease, Type B
- Niemann Pick Disease, Type B
- Niemann-Pick Disease, Visceral
- Niemann Pick Disease, Visceral
- Type B Niemann-Pick Disease
- Type B Niemann Pick Disease
- Niemann-Pick Disease, Non-Neuronopathic Type
- Niemann Pick Disease, Non Neuronopathic Type
- Niemann-Pick's Disease Type B
- Niemann Pick's Disease Type B
Niemann-Pick Disease, Type E- Niemann-Pick Disease, Type E
- Niemann Pick Disease, Type E
- Niemann-Pick's Disease Type E
- Niemann Pick's Disease Type E
- Niemann-Pick Disease, Adult Non-Neuronopathic
- Niemann Pick Disease, Adult Non Neuronopathic
|
Below are MeSH descriptors whose meaning is more general than "Niemann-Pick Disease, Type B".
- 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]
- Lysosomal Storage Diseases, Nervous System [C10.228.140.163.100.435]
- Sphingolipidoses [C10.228.140.163.100.435.825]
- Niemann-Pick Diseases [C10.228.140.163.100.435.825.700]
- Niemann-Pick Disease, Type B [C10.228.140.163.100.435.825.700.750]
- Hemic and Lymphatic Diseases [C15]
- Lymphatic Diseases [C15.604]
- Histiocytosis [C15.604.250]
- Histiocytosis, Non-Langerhans-Cell [C15.604.250.410]
- Niemann-Pick Diseases [C15.604.250.410.625]
- Niemann-Pick Disease, Type B [C15.604.250.410.625.750]
- 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]
- Lysosomal Storage Diseases, Nervous System [C16.320.565.189.435]
- Sphingolipidoses [C16.320.565.189.435.825]
- Niemann-Pick Diseases [C16.320.565.189.435.825.700]
- Niemann-Pick Disease, Type B [C16.320.565.189.435.825.700.750]
- Lipid Metabolism, Inborn Errors [C16.320.565.398]
- Lipidoses [C16.320.565.398.641]
- Sphingolipidoses [C16.320.565.398.641.803]
- Niemann-Pick Diseases [C16.320.565.398.641.803.730]
- Niemann-Pick Disease, Type B [C16.320.565.398.641.803.730.750]
- Lysosomal Storage Diseases [C16.320.565.595]
- Lysosomal Storage Diseases, Nervous System [C16.320.565.595.554]
- Sphingolipidoses [C16.320.565.595.554.825]
- Niemann-Pick Diseases [C16.320.565.595.554.825.700]
- Niemann-Pick Disease, Type B [C16.320.565.595.554.825.700.750]
- Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
- Brain Diseases, Metabolic [C18.452.132]
- Brain Diseases, Metabolic, Inborn [C18.452.132.100]
- Lysosomal Storage Diseases, Nervous System [C18.452.132.100.435]
- Sphingolipidoses [C18.452.132.100.435.825]
- Niemann-Pick Diseases [C18.452.132.100.435.825.700]
- Niemann-Pick Disease, Type B [C18.452.132.100.435.825.700.750]
- Lipid Metabolism Disorders [C18.452.584]
- Lipidoses [C18.452.584.687]
- Sphingolipidoses [C18.452.584.687.803]
- Niemann-Pick Diseases [C18.452.584.687.803.730]
- Niemann-Pick Disease, Type B [C18.452.584.687.803.730.750]
- Metabolism, Inborn Errors [C18.452.648]
- Brain Diseases, Metabolic, Inborn [C18.452.648.189]
- Lysosomal Storage Diseases, Nervous System [C18.452.648.189.435]
- Sphingolipidoses [C18.452.648.189.435.825]
- Niemann-Pick Diseases [C18.452.648.189.435.825.700]
- Niemann-Pick Disease, Type B [C18.452.648.189.435.825.700.750]
- Lipid Metabolism, Inborn Errors [C18.452.648.398]
- Lipidoses [C18.452.648.398.641]
- Sphingolipidoses [C18.452.648.398.641.803]
- Niemann-Pick Diseases [C18.452.648.398.641.803.730]
- Niemann-Pick Disease, Type B [C18.452.648.398.641.803.730.750]
- Lysosomal Storage Diseases [C18.452.648.595]
- Lysosomal Storage Diseases, Nervous System [C18.452.648.595.554]
- Sphingolipidoses [C18.452.648.595.554.825]
- Niemann-Pick Diseases [C18.452.648.595.554.825.700]
- Niemann-Pick Disease, Type B [C18.452.648.595.554.825.700.750]
Below are MeSH descriptors whose meaning is more specific than "Niemann-Pick Disease, Type B".
This graph shows the total number of publications written about "Niemann-Pick Disease, Type B" by people in this website by year, and whether "Niemann-Pick Disease, Type B" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Niemann-Pick Disease, Type B" by people in Profiles.
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Poczobutt JM, Mikosz AM, Poirier C, Beatman EL, Serban KA, Gally F, Cao D, McCubbrey AL, Cornell CF, Schweitzer KS, Berdyshev EV, Bronova IA, Paris F, Petrache I. Altered Macrophage Function Associated with Crystalline Lung Inflammation in Acid Sphingomyelinase Deficiency. Am J Respir Cell Mol Biol. 2021 05; 64(5):629-640.
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