Niemann-Pick Disease, Type B

MeSH code information
  • Name
  • Concept
    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).
  • Tree numbers
    • 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
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