MeSH Browser

MeSH Heading: Niemann-Pick Disease, Type B
Tree 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; C18.452.584.563.641.803.730.750; C18.452.648.189.435.825.700.750; C18.452.648.398.641.803.730.750; C18.452.648.595.554.825.700.750
Unique ID: D052537
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D052537
Scope Note: 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).
Entry Version: NIEMANN PICK DIS TYPE B
Entry Term(s): Niemann-Pick Disease, Adult Non-Neuronopathic; Niemann-Pick Disease, Non-Neuronopathic Type; Niemann-Pick Disease, Type E; Niemann-Pick Disease, Visceral; Niemann-Pick's Disease Type B; Niemann-Pick's Disease Type E; Type B Niemann-Pick Disease
Previous Indexing: Niemann-Pick Diseases (1975-2006)
Public MeSH Note: 2007; see NIEMANN-PICK DISEASES 2000-2006
History Note: 2007; use NIEMANN-PICK DISEASES 2000-2006
Date Established: 2007/01/01
Date of Entry: 2006/07/05
Revision Date: 2021/07/01

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

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 A [C10.228.140.163.100.435.825.700.500]
        
        Niemann-Pick Disease, Type B [C10.228.140.163.100.435.825.700.750]
        
        Niemann-Pick Disease, Type C [C10.228.140.163.100.435.825.700.875]

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 A [C15.604.250.410.625.500]
        
        Niemann-Pick Disease, Type B [C15.604.250.410.625.750]
        
        Niemann-Pick Disease, Type C [C15.604.250.410.625.875]

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 A [C16.320.565.189.435.825.700.500]
        
        Niemann-Pick Disease, Type B [C16.320.565.189.435.825.700.750]
        
        Niemann-Pick Disease, Type C [C16.320.565.189.435.825.700.875]

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
  - Metabolism, Inborn Errors [C16.320.565]
    - 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 A [C16.320.565.398.641.803.730.500]
        
        Niemann-Pick Disease, Type B [C16.320.565.398.641.803.730.750]
        
        Niemann-Pick Disease, Type C [C16.320.565.398.641.803.730.875]

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
  - Metabolism, Inborn Errors [C16.320.565]
    - 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 A [C16.320.565.595.554.825.700.500]
        
        Niemann-Pick Disease, Type B [C16.320.565.595.554.825.700.750]
        
        Niemann-Pick Disease, Type C [C16.320.565.595.554.825.700.875]

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 A [C18.452.132.100.435.825.700.500]
        
        Niemann-Pick Disease, Type B [C18.452.132.100.435.825.700.750]
        
        Niemann-Pick Disease, Type C [C18.452.132.100.435.825.700.875]

Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
  - Lipid Metabolism Disorders [C18.452.584]
    - Lipid Metabolism, Inborn Errors [C18.452.584.563]
      - Lipidoses [C18.452.584.563.641]
        
        Sphingolipidoses [C18.452.584.563.641.803]
        
        Niemann-Pick Diseases [C18.452.584.563.641.803.730]
        
        Niemann-Pick Disease, Type A [C18.452.584.563.641.803.730.500]
        
        Niemann-Pick Disease, Type B [C18.452.584.563.641.803.730.750]
        
        Niemann-Pick Disease, Type C [C18.452.584.563.641.803.730.875]

Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
  - 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 A [C18.452.648.189.435.825.700.500]
        
        Niemann-Pick Disease, Type B [C18.452.648.189.435.825.700.750]
        
        Niemann-Pick Disease, Type C [C18.452.648.189.435.825.700.875]

Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
  - Metabolism, Inborn Errors [C18.452.648]
    - 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 A [C18.452.648.398.641.803.730.500]
        
        Niemann-Pick Disease, Type B [C18.452.648.398.641.803.730.750]
        
        Niemann-Pick Disease, Type C [C18.452.648.398.641.803.730.875]

Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
  - Metabolism, Inborn Errors [C18.452.648]
    - 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 A [C18.452.648.595.554.825.700.500]
        
        Niemann-Pick Disease, Type B [C18.452.648.595.554.825.700.750]
        
        Niemann-Pick Disease, Type C [C18.452.648.595.554.825.700.875]

Niemann-Pick Disease, Type B Preferred

Niemann-Pick Disease, Type E Narrower

Niemann-Pick Disease, Type B MeSH Descriptor Data 2024