Difference between revisions of "Template:Lipid storage disorders"
Jump to navigation
Jump to search
imported>Was a bee m (→top: ICD code exported (from bot request)) |
|||
(15 intermediate revisions by 12 users not shown) | |||
Line 1: | Line 1: | ||
{{Navbox | {{Navbox | ||
− | | 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]]<br />(to [[ceramide]]) | + | | group1 = [[Sphingolipidoses]]<br />(to [[ceramide]]) |
− | | | + | | list1 = {{Navbox|child |
− | | | ||
− | |||
− | | group1 = From [[ganglioside]]<br />([[Gangliosidosis|gangliosidoses]]) | + | | 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]] | + | | group4 = From [[sulfatide]]<br />([[Sulfatidosis|sulfatidoses]] |
− | | list4 | + | * [[leukodystrophy]]) |
− | + | | list4 = | |
+ | * [[Sulfatide]]: [[Metachromatic leukodystrophy]] | ||
+ | * [[Multiple sulfatase deficiency]] | ||
+ | * [[Galactocerebroside]]: [[Krabbe disease]] | ||
− | |group5 | + | | group5 = To [[sphingosine]] |
− | |list5 | + | | list5 = |
+ | * [[Ceramide]]: [[Farber disease]] | ||
− | }} | + | }} |
− | | group2 = [[Neuronal ceroid lipofuscinosis|NCL]] | + | | group2 = [[Neuronal ceroid lipofuscinosis|NCL]] |
− | | | + | | list2 = |
+ | * [[Infantile neuronal ceroid lipofuscinosis|Infantile]] | ||
+ | * [[Jansky–Bielschowsky disease]] | ||
+ | * [[Batten disease]] | ||
− | | group3 = Other | + | | group3 = Other |
− | | | + | | list3 = |
− | + | * [[Cerebrotendineous xanthomatosis]] | |
− | + | * [[Cholesteryl ester storage disease]] ([[Lysosomal acid lipase deficiency]]/[[Wolman disease]]) | |
− | + | * [[Sea-blue histiocytosis]] | |
}}<noinclude> | }}<noinclude> | ||
− | + | {{collapsible option}} | |
− | [[Category:Metabolic disorder templates | + | [[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
.