Difference between revisions of "Template:Lipid storage disorders"
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imported>Arcadian (cat) |
imported>Cobaltcigs |
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{{Navbox | {{Navbox | ||
| name = Lipid storage disorders | | name = Lipid storage disorders | ||
− | | title = ([[Lysosomal storage disease|LSD]]) [[Inborn error of metabolism|Inborn error]] of [[Inborn error of lipid metabolism|lipid metabolism]]: [[lipid storage disorder]]s ([[ICD- | + | | title = ([[Lysosomal storage disease|LSD]]) [[Inborn error of metabolism|Inborn error]] of [[Inborn error of lipid metabolism|lipid metabolism]]: [[lipid storage disorder]]s ([[ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases#(E75) Lipids|E75]], [[List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders#Other metabolic and immunity disorders (270–279)|272.7–272.8]]) |
| state = {{{state|autocollapse}}} | | state = {{{state|autocollapse}}} | ||
| titlestyle = background:Silver | | titlestyle = background:Silver | ||
− | | group1 = [[Sphingolipidoses]]< | + | | group1 = [[Sphingolipidoses]]<br />(to [[ceramide]]) |
| list1 = {{Navbox subgroup | | list1 = {{Navbox subgroup | ||
− | | groupstyle = | + | | groupstyle = |
− | | liststyle = | + | | liststyle = |
− | | group1 = From [[ganglioside]]< | + | | group1 = From [[ganglioside]]<br />([[Gangliosidosis|gangliosidoses]]) |
| list1 = [[Ganglioside]]: [[GM1 gangliosidoses]]{{·}} [[GM2 gangliosidoses]] ([[Sandhoff disease]], [[Tay-Sachs disease]], [[GM2-gangliosidosis, AB variant|AB variant]]) | | list1 = [[Ganglioside]]: [[GM1 gangliosidoses]]{{·}} [[GM2 gangliosidoses]] ([[Sandhoff disease]], [[Tay-Sachs disease]], [[GM2-gangliosidosis, AB variant|AB variant]]) | ||
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|group3 = From [[sphingomyelin]] | |group3 = From [[sphingomyelin]] | ||
− | |list3 = [[Sphingomyelin]]: ''phospholipid:'' [[Niemann-Pick disease]] ([[Niemann-Pick disease, SMPD1-associated|SMPD1-associated]], [[Niemann-Pick disease, type C|type C]])< | + | |list3 = <div>[[Sphingomyelin]]: ''phospholipid:'' [[Niemann-Pick disease]] ([[Niemann-Pick disease, SMPD1-associated|SMPD1-associated]], [[Niemann-Pick disease, type C|type C]])</div> |
+ | <div>[[Glucocerebroside]]: [[Gaucher's disease]]</div> | ||
− | + | | group4 = From [[sulfatide]]<br />([[Sulfatidosis|sulfatidoses]], [[leukodystrophy]]) | |
− | + | | list4 = <div>[[Sulfatide]]: [[Metachromatic leukodystrophy]]{{·}} [[Multiple sulfatase deficiency]]</div> | |
− | | group4 = From [[sulfatide]]< | + | <div>[[Galactocerebroside]]: [[Krabbe disease]]</div> |
− | | list4 = [[Sulfatide]]: [[Metachromatic leukodystrophy]]{{·}} [[Multiple sulfatase deficiency]]< | ||
− | |||
− | [[Galactocerebroside]]: [[Krabbe disease]] | ||
|group5 = To [[sphingosine]] | |group5 = To [[sphingosine]] | ||
|list5 = [[Ceramide]]: [[Farber disease]] | |list5 = [[Ceramide]]: [[Farber disease]] | ||
− | }} | + | }} |
− | |||
| group2 = [[Neuronal ceroid lipofuscinosis|NCL]] | | group2 = [[Neuronal ceroid lipofuscinosis|NCL]] | ||
− | | list2 = [[Infantile neuronal ceroid lipfuscinosis|Infantile]]{{·}} [[Jansky-Bielschowsky disease]]{{·}} [[Batten disease]] | + | | list2 = [[Infantile neuronal ceroid lipfuscinosis|Infantile]]{{·}} [[Jansky-Bielschowsky disease]]{{·}} [[Batten disease]] |
| group3 = Other | | group3 = Other | ||
| list3 = [[Cerebrotendineous xanthomatosis]]{{·}} [[Cholesteryl ester storage disease]] ([[Wolman disease]]){{·}} [[Sea-blue histiocyte syndrome]] | | list3 = [[Cerebrotendineous xanthomatosis]]{{·}} [[Cholesteryl ester storage disease]] ([[Wolman disease]]){{·}} [[Sea-blue histiocyte syndrome]] | ||
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| below = {{Metabolic navs}} | | below = {{Metabolic navs}} | ||