Niemann-Pick Disease, Type B

MeSH code information

• Name
  Niemann-Pick Disease, Type B
• 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
• Qualifiers
  diagnosis, parasitology, immunology, microbiology, diagnostic imaging, physiopathology, rehabilitation, enzymology, etiology, mortality, epidemiology, blood, cerebrospinal fluid, chemically induced, diet therapy, drug therapy, therapy, psychology, urine, virology, veterinary, history, classification, economics, embryology, genetics, nursing, radiotherapy, ethnology, prevention & control, pathology, metabolism, complications, surgery