Difference between revisions of "Template:Inborn errors of purine–pyrimidine metabolism"

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{{Navbox
 
{{Navbox
| name  = Inborn errors of purine-pyrimidine metabolism
+
| name  = Inborn errors of purine–pyrimidine metabolism
| title = [[Inborn error of metabolism|Inborn error]] of  [[Inborn errors of purine-pyrimidine metabolism|purine-pyrimidine metabolism]] ([[ICD-10_Chapter_IV:_Endocrine%2C_nutritional_and_metabolic_diseases#.28E79-E90.29_Other_metabolic_disorders|E79]], [[List_of_ICD-9_codes_240-279:_Endocrine%2C_nutritional_and_metabolic_diseases%2C_and_immunity_disorders#other_metabolic_and_immunity_disorders_.28270-279.29|277.2]])
+
| title = [[Inborn error of metabolism|Inborn error]] of  [[Inborn errors of purine–pyrimidine metabolism|purine–pyrimidine metabolism]]
 +
|listclass = hlist
 
| state = {{{state|autocollapse}}}
 
| state = {{{state|autocollapse}}}
| titlestyle = background:Silver
 
  
 
| group1 = [[Purine metabolism]]
 
| group1 = [[Purine metabolism]]
|  list1 = {{Navbox subgroup
+
|  list1 = {{Navbox|subgroup
  
 
   | group1 = Anabolism
 
   | group1 = Anabolism
   |  list1 = [[Adenylosuccinate lyase deficiency]]{{·}} [[Myoadenylate deaminase deficiency]]
+
   |  list1 =
 +
* [[Adenylosuccinate lyase deficiency]]
 +
* [[Adenosine Monophosphate Deaminase Deficiency type 1]]
  
 
   | group2 = [[Nucleotide salvage]]
 
   | group2 = [[Nucleotide salvage]]
   | list2  = [[Lesch–Nyhan syndrome|Lesch-Nyhan syndrome]]/[[Hyperuricemia]]{{·}} [[Adenine phosphoribosyltransferase deficiency]]
+
   | list2  =
 +
* [[Lesch–Nyhan syndrome]]/[[Hyperuricemia]]
 +
* [[Adenine phosphoribosyltransferase deficiency]]
  
 
   | group3 = Catabolism
 
   | group3 = Catabolism
   |  list3 = [[Adenosine deaminase deficiency]]{{·}} [[Purine nucleoside phosphorylase deficiency]]{{·}} [[Xanthinuria]]{{·}} [[Gout]]
+
   |  list3 =
 +
* [[Adenosine deaminase deficiency]]
 +
* [[Purine nucleoside phosphorylase deficiency]]
 +
* [[Xanthinuria]]
 +
* [[Gout]]
 +
* [[Mitochondrial neurogastrointestinal encephalopathy syndrome]]
  
 
}}
 
}}
  
 
| group2 = [[Pyrimidine metabolism]]
 
| group2 = [[Pyrimidine metabolism]]
|  list2 = {{Navbox subgroup
+
|  list2 = {{Navbox|subgroup
  
 
   | group1 = Anabolism
 
   | group1 = Anabolism
   |  list1 = [[Orotic aciduria]]{{·}} [[Miller syndrome]]
+
   |  list1 =
 +
* [[Orotic aciduria]]
 +
* [[Miller syndrome]]
  
 
   | group2 = Catabolism
 
   | group2 = Catabolism
   | list2  = [[Dihydropyrimidine dehydrogenase deficiency]]
+
   | list2  =
 +
* [[Dihydropyrimidine dehydrogenase deficiency]]
  
 
}}
 
}}
  
| group4 =
+
}}<noinclude>
|  list4 = 
+
{{collapsible option}}
 
+
[[Category:Inborn errors of purine-pyrimidine metabolism]]
| group5 =
+
[[Category:Metabolic disorder templates]]
|  list5 =
+
</noinclude>
 
 
| below = {{Metabolic navs}}
 
 
 
}}
 
<noinclude>[[Category:Inborn errors of metabolism]][[Category:Metabolic disorder templates|{{PAGENAME}}]]</noinclude>
 

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 purine–pyrimidine metabolism|state=collapsed}} to show the template collapsed, i.e., hidden apart from its title bar
  • |state=expanded: {{Inborn errors of purine–pyrimidine metabolism|state=expanded}} to show the template expanded, i.e., fully visible
  • |state=autocollapse: {{Inborn errors of purine–pyrimidine 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.