Difference between revisions of "Template:Glycoprotein disorders"

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imported>Arcadian
(Dolichol kinase deficiency)
imported>Arcadian
(+1, -1, grouping)
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{{Navbox
 
{{Navbox
 
| name  = Glycoproteinoses
 
| name  = Glycoproteinoses
| title = ([[Lysosomal storage disease|LSD]]) [[Inborn error of metabolism|Inborn error]] of [[Inborn errors of carbohydrate metabolism|carbohydrate metabolism]]: [[glycoproteinosis]]/[[mucolipidosis]] ([[ICD-10_Chapter_IV:_Endocrine,_nutritional_and_metabolic_diseases#.28E76-E78.29_Combinations|E77]], [[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|     272.7]])
+
| 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#.28E76-E78.29_Combinations|E77]], [[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|271.8]])
 
| state = {{{state|autocollapse}}}
 
| state = {{{state|autocollapse}}}
 
| titlestyle = background:Silver
 
| titlestyle = background:Silver
  
| group1 = [[Post-translational modification]]<BR>of [[lysosomal enzymes]]
+
| group1 = Anabolism
|  list1 = [[I-cell disease|I-cell disease/II]]{{·}} [[Pseudo-Hurler polydystrophy|Pseudo-Hurler polydystrophy/III]]
+
|  list1 = [[Dolichol kinase deficiency]]{{·}} [[Congenital disorder of glycosylation]]
  
| group2 = Glycoprotein degradation
+
| group2 = [[Post-translational modification]]<BR>of [[lysosomal enzymes]]
|  list2 = [[Aspartylglucosaminuria]]{{·}} [[Fucosidosis]]{{·}} ''[[mannosidosis]]'' ([[Alpha-mannosidosis]], [[Beta-mannosidosis]]) - [[Sialidosis|Sialidosis/I]]
+
|  list2 = [[Mucolipidosis]]: [[I-cell disease|I-cell disease/II]]{{·}} [[Pseudo-Hurler polydystrophy|Pseudo-Hurler polydystrophy/III]]
  
| group3 = Other
+
| group3 = Glycoprotein degradation
|  list3 = ''[[channelopathy]]'' ([[Mucolipidosis type IV]]){{·}} ''[[solute carrier family]]'' ([[Salla disease]]){{·}} [[Galactosialidosis]]<BR>
+
|  list3 = [[Aspartylglucosaminuria]]{{·}} [[Fucosidosis]]{{·}} ''[[mannosidosis]]'' ([[Alpha-mannosidosis]], [[Beta-mannosidosis]]){{·}} [[Sialidosis]]
  
anabolism: [[Dolichol kinase deficiency]]
+
| group4 = Other
 
+
|  list4 = ''[[solute carrier family]]'' ([[Salla disease]]){{·}} [[Galactosialidosis]]<BR>
| group4 =  
 
|  list4 =  
 
  
 
| group5 =  
 
| group5 =  

Revision as of 15:03, 3 November 2010