Difference between revisions of "Template:Heme metabolism disorders"

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{{Navbox
 
{{Navbox
| name = Heme metabolism disorders
+
| name = Heme metabolism disorders
| title = [[Heme]] metabolism disorders ([[ICD-10_Chapter_IV:_Endocrine%2C_nutritional_and_metabolic_diseases#.28E79-E90.29_Other_metabolic_disorders|E80]], [[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|277.1, 277.4]])
+
| state = {{{state<includeonly>|autocollapse</includeonly>}}}
| state = {{{state|autocollapse}}}
 
| titlestyle = background:Silver
 
  
| group2 = [[Porphyria]],<BR>[[Hepatic porphyria|hepatic]] and [[Erythropoietic porphyria|erythropoietic]]<BR>([[porphyrin]])
+
| title = [[Heme]] metabolism disorders
|  list2 = ''early mitochondrial:'' [[Aminolevulinic acid dehydratase deficiency porphyria|ALAD porphyria]]{{·}} [[Acute intermittent porphyria]]
 
  
''cytoplasmic:'' [[Gunther disease|Gunther disease/congenital erythropoietic porphyria]]{{·}} [[Porphyria cutanea tarda]]/[[Hepatoerythropoietic porphyria]]
+
| listclass = hlist
  
''late mitochondrial:'' [[Hereditary coproporphyria]]{{·}} [[Variegate porphyria]]{{·}} [[Erythropoietic protoporphyria]]
+
| group2 = [[Porphyria]],<br />[[Hepatic porphyria|hepatic]] and [[Erythropoietic porphyria|erythropoietic]]<br />([[porphyrin]])
 +
| list2 = {{Navbox|child
  
| group3 = [[Hereditary hyperbilirubinemia]]<BR>([[bilirubin]])
+
  | group1 = {{nobold|''early mitochondrial:''}}
| list3 = ''unconjugated:'' [[Gilbert's syndrome]]{{·}} [[Crigler-Najjar syndrome]]{{·}} [[Lucey-Driscoll syndrome]]<BR>
+
  | list1 =
 +
* [[Aminolevulinic acid dehydratase deficiency porphyria|ALAD porphyria]]
 +
* [[Acute intermittent porphyria]]
  
''conjugated:'' [[Dubin–Johnson syndrome]]{{·}} [[Rotor syndrome]]
+
  | group2 = {{nobold|''cytoplasmic:''}}
 +
  | list2 =
 +
* [[Gunther disease|Gunther disease/congenital erythropoietic porphyria]]
 +
* [[Porphyria cutanea tarda]]/[[Hepatoerythropoietic porphyria]]
  
 +
  | group3 = {{nobold|''late mitochondrial:''}}
 +
  | list3 =
 +
* [[Hereditary coproporphyria]]
 +
* [[Harderoporphyria]]
 +
* [[Variegate porphyria]]
 +
* [[Erythropoietic protoporphyria]]
  
| below = {{Metabolic navs}}{{Myeloid navs}}
+
}}
  
}}
+
| group3 = [[Hereditary hyperbilirubinemia]]<br />([[bilirubin]])
<noinclude>
+
| list3 = {{Navbox|child
[[Category:Inborn errors of metabolism]]
+
 
[[Category:Metabolic disorder templates|{{PAGENAME}}]]
+
  | group1 = {{nobold|''unconjugated:''}}
 +
  | list1 =
 +
* [[Gilbert's syndrome]]
 +
* [[Crigler–Najjar syndrome]]
 +
* [[Lucey–Driscoll syndrome]]
 +
 
 +
  | group2 = {{nobold|''conjugated:''}}
 +
  | list2 =
 +
* [[Dubin–Johnson syndrome nd sheet]]
 +
* [[Rotor syndrome]]
 +
 
 +
}}
 +
 
 +
}}<noinclude>
 +
{{collapsible option}}
 +
[[Category:Heme metabolism disorders]]
 +
[[Category:Metabolic disorder templates]]
 
</noinclude>
 
</noinclude>

Latest revision as of 13:40, 15 December 2020

Initial visibility: currently defaults to autocollapse

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

  • |state=collapsed: {{Heme metabolism disorders|state=collapsed}} to show the template collapsed, i.e., hidden apart from its title bar
  • |state=expanded: {{Heme metabolism disorders|state=expanded}} to show the template expanded, i.e., fully visible
  • |state=autocollapse: {{Heme metabolism disorders|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.