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 | + | | 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 = | + | | group1 = Anabolism |
| − | | list1 = [[ | + | | list1 = [[Dolichol kinase deficiency]]{{·}} [[Congenital disorder of glycosylation]] |
| − | | group2 = | + | | group2 = [[Post-translational modification]]<BR>of [[lysosomal enzymes]] |
| − | | list2 = [[ | + | | list2 = [[Mucolipidosis]]: [[I-cell disease|I-cell disease/II]]{{·}} [[Pseudo-Hurler polydystrophy|Pseudo-Hurler polydystrophy/III]] |
| − | | group3 = | + | | group3 = Glycoprotein degradation |
| − | | list3 = | + | | list3 = [[Aspartylglucosaminuria]]{{·}} [[Fucosidosis]]{{·}} ''[[mannosidosis]]'' ([[Alpha-mannosidosis]], [[Beta-mannosidosis]]){{·}} [[Sialidosis]] |
| − | + | | group4 = Other | |
| − | + | | list4 = ''[[solute carrier family]]'' ([[Salla disease]]){{·}} [[Galactosialidosis]]<BR> | |
| − | | group4 = | ||
| − | | list4 = | ||
| group5 = | | group5 = | ||