Difference between revisions of "Template:Inborn errors of carbohydrate metabolism"

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imported>Tony Mach
(Slight reformatting, mainly the lysomal group)
imported>Was a bee
m (→‎top: ICD code exported (from bot request))
 
(One intermediate revision by one other user not shown)
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{{Navbox
 
{{Navbox
 
  | name = Inborn errors of carbohydrate metabolism
 
  | name = Inborn errors of carbohydrate metabolism
  | title = [[Inborn error of metabolism|Inborn error]] of [[Inborn errors of carbohydrate metabolism|carbohydrate metabolism]]: [[monosaccharide]] metabolism disorders ([[ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases#(E73–E74) Carbohydrates|E73–E74]], [[List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders#Disorders of carbohydrate transport and metabolism|271]]) <br/> Including [[glycogen storage disease]]s (GSD)
+
  | title = [[Inborn error of metabolism|Inborn error]] of [[Inborn errors of carbohydrate metabolism|carbohydrate metabolism]]: [[monosaccharide]] metabolism disorders <br/> Including [[glycogen storage disease]]s (GSD)
 
  | state = {{{state<includeonly>|autocollapse</includeonly>}}}
 
  | state = {{{state<includeonly>|autocollapse</includeonly>}}}
 
  | listclass = hlist
 
  | listclass = hlist
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     | group1 = {{nobold|Extralysosomal:}}
 
     | group1 = {{nobold|Extralysosomal:}}
 
     | list1 =
 
     | list1 =
 +
* [[Glycogen storage disease type III|GSD type III]] (Cori's disease, debranching enzyme deficiency)
 +
* [[Glycogen storage disease type VI|GSD type VI]] (Hers' disease, liver glycogen phosphorylase deficiency)
 
* [[Glycogen storage disease type V|GSD type V]] (McArdle's disease, myophosphorylase deficiency)  
 
* [[Glycogen storage disease type V|GSD type V]] (McArdle's disease, myophosphorylase deficiency)  
* [[Glycogen storage disease type VI|GSD type VI]] (Hers' disease, liver glycogen phosphorylase deficiency)
+
* [[Glycogen storage disease type IX|GSD type IX]] (phosphorylase kinase deficiency)
* [[Glycogen storage disease type III|GSD type III]] Cori's disease, debranching enzyme deficiency)
 
* [[Glycogen storage disease type IX|GSD type IX]]
 
  
 
     | group2 = {{nobold|[[Lysosome|Lysosomal]] ([[Lysosomal storage disease|LSD]]):}}  
 
     | group2 = {{nobold|[[Lysosome|Lysosomal]] ([[Lysosomal storage disease|LSD]]):}}  

Latest revision as of 21:28, 13 August 2020

Initial visibility: currently defaults to autocollapse

To set this template's initial visibility, the |state= parameter may be used:

  • |state=collapsed: {{Inborn errors of carbohydrate metabolism|state=collapsed}} to show the template collapsed, i.e., hidden apart from its title bar
  • |state=expanded: {{Inborn errors of carbohydrate metabolism|state=expanded}} to show the template expanded, i.e., fully visible
  • |state=autocollapse: {{Inborn errors of carbohydrate metabolism|state=autocollapse}}
    • shows the template collapsed to the title bar if there is a {{navbar}}, a {{sidebar}}, or some other table on the page with the collapsible attribute
    • shows the template in its expanded state if there are no other collapsible items on the page

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.