Difference between revisions of "Template:Lipid storage disorders"
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imported>Arcadian m (clean up - cats using AWB) |
imported>Was a bee m (→top: ICD code exported (from bot request)) |
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| − | | name | + | | name = Lipid storage disorders |
| − | | title = | + | | title = [[Lysosomal storage disease]]s: [[Inborn error of metabolism|Inborn error]]s of [[Inborn error of lipid metabolism|lipid metabolism]] ([[Lipid storage disorder]]s) |
| − | | state = {{{state|autocollapse}}} | + | | state = {{{state<includeonly>|autocollapse</includeonly>}}} |
| − | | | + | | listclass = hlist |
| − | | group1 = [[Sphingolipidoses]]< | + | | group1 = [[Sphingolipidoses]]<br />(to [[ceramide]]) |
| − | | | + | | list1 = {{Navbox|child |
| − | | | ||
| − | |||
| − | | group1 = From [[ganglioside]]< | + | | group1 = From [[ganglioside]]<br />([[Gangliosidosis|gangliosidoses]]) |
| − | | list1 | + | | list1 = |
| + | * [[Ganglioside]]: [[GM1 gangliosidoses]] | ||
| + | * [[GM2 gangliosidoses]] ([[Sandhoff disease]] | ||
| + | * [[Tay–Sachs disease]] | ||
| + | * [[GM2-gangliosidosis, AB variant|AB variant]]) | ||
| − | | group2 = From [[globoside]] | + | | group2 = From [[globoside]] |
| − | | list2 | + | | list2 = |
| + | * [[Globotriaosylceramide]]: [[Fabry disease|Fabry's disease]] | ||
| − | |group3 | + | | group3 = From [[sphingomyelin]] |
| − | |list3 | + | | list3 = |
| + | * [[Sphingomyelin]]: ''phospholipid:'' [[Niemann–Pick disease]] ([[Niemann–Pick disease, SMPD1-associated|SMPD1-associated]] | ||
| + | * [[Niemann–Pick disease, type C|type C]]) | ||
| + | * [[Glucocerebroside]]: [[Gaucher's disease]] | ||
| − | [[ | + | | group4 = From [[sulfatide]]<br />([[Sulfatidosis|sulfatidoses]] |
| + | * [[leukodystrophy]]) | ||
| + | | list4 = | ||
| + | * [[Sulfatide]]: [[Metachromatic leukodystrophy]] | ||
| + | * [[Multiple sulfatase deficiency]] | ||
| + | * [[Galactocerebroside]]: [[Krabbe disease]] | ||
| − | | | + | | group5 = To [[sphingosine]] |
| − | | | + | | list5 = |
| + | * [[Ceramide]]: [[Farber disease]] | ||
| − | + | }} | |
| − | | | + | | group2 = [[Neuronal ceroid lipofuscinosis|NCL]] |
| − | | | + | | list2 = |
| + | * [[Infantile neuronal ceroid lipofuscinosis|Infantile]] | ||
| + | * [[Jansky–Bielschowsky disease]] | ||
| + | * [[Batten disease]] | ||
| − | + | | group3 = Other | |
| − | + | | list3 = | |
| − | + | * [[Cerebrotendineous xanthomatosis]] | |
| − | + | * [[Cholesteryl ester storage disease]] ([[Lysosomal acid lipase deficiency]]/[[Wolman disease]]) | |
| − | + | * [[Sea-blue histiocytosis]] | |
| − | |||
| − | | group3 = Other | ||
| − | | | ||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
| − | |||
}}<noinclude> | }}<noinclude> | ||
| − | [[Category:Metabolic disorder templates | + | {{collapsible option}} |
| + | [[Category:Metabolic disorder templates]] | ||
</noinclude> | </noinclude> | ||
Latest revision as of 21:29, 13 August 2020
Initial visibility: currently defaults to autocollapse
To set this template's initial visibility, the |state= parameter may be used:
|state=collapsed:{{Lipid storage disorders|state=collapsed}}to show the template collapsed, i.e., hidden apart from its title bar|state=expanded:{{Lipid storage disorders|state=expanded}}to show the template expanded, i.e., fully visible|state=autocollapse:{{Lipid storage disorders|state=autocollapse}}
If the |state= parameter in the template on this page is not set, the template's initial visibility is taken from the |default= parameter in the Collapsible option template. For the template on this page, that currently evaluates to autocollapse.