 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
|
| 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".
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