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Niemann-Pick Diseases
Hierarchy: | ∟ ∟ ∟ ∟ ∟ ∟ ∟ Niemann-Pick Diseases 10 coordinate concepts3 subordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Niemann-Pick Diseases 10 coordinate concepts3 subordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Niemann-Pick Diseases 10 coordinate concepts3 subordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Niemann-Pick Diseases 10 coordinate concepts3 subordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Niemann-Pick Diseases 10 coordinate concepts3 subordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Niemann-Pick Diseases 10 coordinate concepts3 subordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Niemann-Pick Diseases 10 coordinate concepts3 subordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Niemann-Pick Diseases 10 coordinate concepts3 subordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Niemann-Pick Diseases 10 coordinate concepts3 subordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Niemann-Pick Diseases 10 coordinate concepts3 subordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Niemann-Pick Diseases 10 coordinate concepts3 subordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Niemann-Pick Diseases 10 coordinate concepts3 subordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Niemann-Pick Diseases 10 coordinate concepts3 subordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ |
Broader terms: | ∟ ∟ ∟ ∟ ∟ ∟ ∟ Niemann-Pick Diseases ∟ ∟ ∟ ∟ ∟ ∟ ∟ Niemann-Pick Diseases ∟ ∟ ∟ ∟ ∟ ∟ ∟ Niemann-Pick Diseases ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Niemann-Pick Diseases ∟ ∟ ∟ ∟ ∟ ∟ Niemann-Pick Diseases ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Niemann-Pick Diseases ∟ ∟ ∟ ∟ ∟ ∟ ∟ Niemann-Pick Diseases ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Niemann-Pick Diseases ∟ ∟ ∟ ∟ ∟ ∟ ∟ Niemann-Pick Diseases ∟ ∟ ∟ ∟ ∟ ∟ Niemann-Pick Diseases ∟ ∟ ∟ ∟ ∟ ∟ ∟ Niemann-Pick Diseases ∟ ∟ ∟ ∟ ∟ ∟ ∟ Niemann-Pick Diseases ∟ ∟ ∟ ∟ ∟ ∟ ∟ Niemann-Pick Diseases |
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Annotation: | note specific types are available
X |
historyNote*: | 2000(1966)
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publicMeSHNote*: | 2000; see NIEMANN-PICK DISEASE 1966-1999
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Scope note: | A group of autosomal recessive disorders in which harmful quantities of lipids accumulate in the viscera and the central nervous system. They can be caused by deficiencies of enzyme activities (SPHINGOMYELIN PHOSPHODIESTERASE) or defects in intracellular transport, resulting in the accumulation of SPHINGOMYELINS and CHOLESTEROL. There are various subtypes based on their clinical and genetic differences.
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activeMeSHYear*: | 2007X |
dateCreated*: | 1999-01-01X |
dateRevised*: | 2006-07-05X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | lktX |
recordOriginator*: | NLMX |
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Labels and equivalent concepts: | Niemann-Pickin taudit (fi) XSfingomyeliinilipidoosit (fi, replaced) Sfingomyeliinilipidoosi (fi, replaced) Niemann-Pickin tauti (fi, replaced) Niemann-Picks sjukdomar (sv) Niemann-Pick Disease (en, replaced) Morbus Niemann-Pick (la-FI, replaced) |
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