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]])
+
| title = [[Heme]] metabolism disorders ([[ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases#(E79–E90) Other metabolic disorders|E80]], [[List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders#Other metabolic and immunity disorders (270–279)|277.1, 277.4]])
 
| state = {{{state|autocollapse}}}
 
| state = {{{state|autocollapse}}}
 
| titlestyle = background:Silver
 
| titlestyle = background:Silver
  
| group2 = [[Porphyria]],<BR>[[Hepatic porphyria|hepatic]] and [[Erythropoietic porphyria|erythropoietic]]<BR>([[porphyrin]])
+
| group2 = [[Porphyria]],<br />[[Hepatic porphyria|hepatic]] and [[Erythropoietic porphyria|erythropoietic]]<br />([[porphyrin]])
|  list2 = ''early mitochondrial:'' [[Aminolevulinic acid dehydratase deficiency porphyria|ALAD porphyria]]{{·}} [[Acute intermittent porphyria]]
+
|  list2 = <div>''early mitochondrial:'' [[Aminolevulinic acid dehydratase deficiency porphyria|ALAD porphyria]]{{·}} [[Acute intermittent porphyria]]</div>
 
+
<div>''cytoplasmic:'' [[Gunther disease|Gunther disease/congenital erythropoietic porphyria]]{{·}} [[Porphyria cutanea tarda]]/[[Hepatoerythropoietic porphyria]]</div>
''cytoplasmic:'' [[Gunther disease|Gunther disease/congenital erythropoietic porphyria]]{{·}} [[Porphyria cutanea tarda]]/[[Hepatoerythropoietic porphyria]]
+
<div>''late mitochondrial:'' [[Hereditary coproporphyria]]{{·}} [[Variegate porphyria]]{{·}} [[Erythropoietic protoporphyria]]</div>
 
 
''late mitochondrial:'' [[Hereditary coproporphyria]]{{·}} [[Variegate porphyria]]{{·}} [[Erythropoietic protoporphyria]]
 
 
 
| group3 = [[Hereditary hyperbilirubinemia]]<BR>([[bilirubin]])
 
|  list3 = ''unconjugated:'' [[Gilbert's syndrome]]{{·}} [[Crigler-Najjar syndrome]]{{·}} [[Lucey-Driscoll syndrome]]<BR>
 
 
 
''conjugated:'' [[Dubin–Johnson syndrome]]{{·}} [[Rotor syndrome]]
 
 
 
  
 +
| group3 = [[Hereditary hyperbilirubinemia]]<br />([[bilirubin]])
 +
|  list3 = <div>''unconjugated:'' [[Gilbert's syndrome]]{{·}} [[Crigler-Najjar syndrome]]{{·}} [[Lucey-Driscoll syndrome]]</div>
 +
<div>''conjugated:'' [[Dubin–Johnson syndrome]]{{·}} [[Rotor syndrome]]</div>
 +
| belowstyle = padding:0px;
 
| below = {{Metabolic navs}}{{Myeloid navs}}
 
| below = {{Metabolic navs}}{{Myeloid navs}}
  
}}
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}}<noinclude>
<noinclude>
 
 
[[Category:Inborn errors of metabolism]]
 
[[Category:Inborn errors of metabolism]]
 
[[Category:Metabolic disorder templates|{{PAGENAME}}]]
 
[[Category:Metabolic disorder templates|{{PAGENAME}}]]
 
</noinclude>
 
</noinclude>

Revision as of 23:27, 21 December 2010