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

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imported>Tony Mach
(Added GSD-IX)
imported>Tony Mach
(Reformatted the GSDs)
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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 (including [[glycogen storage disease]]s) ([[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]])
+
  | title = [[Inborn error of metabolism|Inborn error]] of [[Inborn errors of carbohydrate metabolism|carbohydrate metabolism]]: [[monosaccharide]] metabolism disorders, including [[glycogen storage disease]]s (GSDs) ([[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]])
 
  | state = {{{state<includeonly>|autocollapse</includeonly>}}}
 
  | state = {{{state<includeonly>|autocollapse</includeonly>}}}
 
  | listclass = hlist
 
  | listclass = hlist
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   | group1 = [[Glycogenesis]]
 
   | group1 = [[Glycogenesis]]
 
   | list1 =
 
   | list1 =
* [[Glycogen storage disease type 0|GSD type 0, glycogen synthase]]
+
* [[Glycogen storage disease type 0|GSD type 0]] (glycogen synthase deficiency)
* [[Glycogen storage disease type IV|GSD type IV, Andersen's, branching]]
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* [[Glycogen storage disease type IV|GSD type IV]] (Andersen's disease, branching enzyme deficiency)
* [[Adult polyglucosan body disease]]
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* [[Adult polyglucosan body disease]] (APBD)
  
 
   | group2 = [[Glycogenolysis]]
 
   | group2 = [[Glycogenolysis]]
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     | group1 = {{nobold|extralysosomal:}}
 
     | group1 = {{nobold|extralysosomal:}}
 
     | list1 =
 
     | list1 =
* [[Glycogen storage disease type V|GSD type V, McArdle, muscle glycogen phosphorylase]]/[[Glycogen storage disease type VI|GSD type VI, Hers', liver glycogen phosphorylase]]
+
* [[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 III|GSD type III, Cori's, debranching]]
+
* [[Glycogen storage disease type III|GSD type III]] Cori's disease, debranching enzyme deficiency)
 
     | list2 =
 
     | list2 =
* [[Lysosome|lysosomal]]/[[Lysosomal storage disease|LSD]]: [[Glycogen storage disease type II|GSD type II, Pompe's, glucosidase]]
+
* [[Lysosome|lysosomal]]/[[Lysosomal storage disease|LSD]]: [[Glycogen storage disease type II|GSD type II]] (Pompe's disease, glucosidase deficiency)
* [[Glycogen storage disease type IX]]
+
* [[Glycogen storage disease type IX|GSD type IX]]
  
 
   }}
 
   }}
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   | list1 =
 
   | list1 =
 
* [[MODY 2]]/[[Hyperinsulinemic hypoglycemia|HHF3]]
 
* [[MODY 2]]/[[Hyperinsulinemic hypoglycemia|HHF3]]
* [[Phosphofructokinase deficiency|GSD type VII, Tarui's, phosphofructokinase]]
+
* [[Phosphofructokinase deficiency|GSD type VII]] (Tarui's disease, phosphofructokinase deficiency)
 
* [[Triosephosphate isomerase deficiency]]
 
* [[Triosephosphate isomerase deficiency]]
 
* [[Pyruvate kinase deficiency]]
 
* [[Pyruvate kinase deficiency]]
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* [[Pyruvate carboxylase deficiency|PCD]]
 
* [[Pyruvate carboxylase deficiency|PCD]]
 
* [[Fructose bisphosphatase deficiency]]
 
* [[Fructose bisphosphatase deficiency]]
* [[Glycogen storage disease type I|GSD type I, von Gierke, glucose 6-phosphatase]]
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* [[Glycogen storage disease type I|GSD type I]] (von Gierke's disease, glucose 6-phosphatase deficiency)
  
 
  }}
 
  }}

Revision as of 07:28, 15 December 2017

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.