Difference between revisions of "Template:Glycoprotein disorders"

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imported>Arcadian
(cat)
imported>WOSlinker
(use listclass = hlist in navbox as per WP:HLIST)
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| name  = Glycoprotein disorders
 
| name  = Glycoprotein disorders
 
| title = ([[Lysosomal storage disease|LSD]]) [[Inborn error of metabolism|Inborn error]] of [[Inborn errors of carbohydrate metabolism|carbohydrate metabolism]]: [[glycoproteinosis]] ([[ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases#(E76–E78) Combinations|E77]], [[List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders#Other metabolic and immunity disorders (270–279)|271.8]])
 
| title = ([[Lysosomal storage disease|LSD]]) [[Inborn error of metabolism|Inborn error]] of [[Inborn errors of carbohydrate metabolism|carbohydrate metabolism]]: [[glycoproteinosis]] ([[ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases#(E76–E78) Combinations|E77]], [[List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders#Other metabolic and immunity disorders (270–279)|271.8]])
 +
|listclass = hlist
 
| state = {{{state|autocollapse}}}
 
| state = {{{state|autocollapse}}}
 
| titlestyle = background:Silver
 
| titlestyle = background:Silver
  
 
| group1 = Anabolism
 
| group1 = Anabolism
|  list1 = [[Dolichol kinase deficiency]]{{·}} [[Congenital disorder of glycosylation]]
+
|  list1 =
 +
* [[Dolichol kinase deficiency]]
 +
* [[Congenital disorder of glycosylation]]
  
 
| group2 = [[Post-translational modification]]<br />of [[lysosomal enzymes]]
 
| group2 = [[Post-translational modification]]<br />of [[lysosomal enzymes]]
|  list2 = [[Mucolipidosis]]: [[I-cell disease|I-cell disease/II]]{{·}} [[Pseudo-Hurler polydystrophy|Pseudo-Hurler polydystrophy/III]]
+
|  list2 =
 +
* [[Mucolipidosis]]: [[I-cell disease|I-cell disease/II]]
 +
* [[Pseudo-Hurler polydystrophy|Pseudo-Hurler polydystrophy/III]]
  
 
| group3 = Catabolism
 
| group3 = Catabolism
|  list3 = [[Aspartylglucosaminuria]]{{·}} [[Fucosidosis]]{{·}} ''[[mannosidosis]]'' ([[Alpha-mannosidosis]], [[Beta-mannosidosis]]){{·}} [[Sialidosis]]{{·}} [[Schindler disease]]
+
|  list3 =
 +
* [[Aspartylglucosaminuria]]
 +
* [[Fucosidosis]]
 +
* ''[[mannosidosis]]''
 +
** [[Alpha-mannosidosis]]
 +
** [[Beta-mannosidosis]]
 +
* [[Sialidosis]]
 +
* [[Schindler disease]]
  
 
| group4 = Other
 
| group4 = Other
|  list4 = ''[[solute carrier family]]'' ([[Salla disease]]){{·}} [[Galactosialidosis]]
+
|  list4 =
 +
* ''[[solute carrier family]]'' ([[Salla disease]])
 +
* [[Galactosialidosis]]
  
 
| belowstyle = background: transparent; padding: 0px;
 
| belowstyle = background: transparent; padding: 0px;
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}}<noinclude>
 
}}<noinclude>
 
[[Category:Glycoprotein metabolism disorders]]
 
[[Category:Glycoprotein metabolism disorders]]
[[Category:Metabolic disorder templates|{{PAGENAME}}]]
+
[[Category:Metabolic disorder templates]]
 
</noinclude>
 
</noinclude>

Revision as of 21:38, 10 October 2012