Difference between revisions of "Template:Inborn errors of carbohydrate metabolism"
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imported>Arcadian (cat) |
imported>Cobaltcigs |
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{{Navbox | {{Navbox | ||
| name = Inborn errors of carbohydrate metabolism | | name = Inborn errors of carbohydrate metabolism | ||
| − | | title = [[Inborn error of metabolism|Inborn error]] of [[Inborn errors of carbohydrate metabolism|carbohydrate metabolism]]: [[monosaccharide]] metabolism disorders (including [[glycogen storage disease]]s) ([[ICD- | + | | title = [[Inborn error of metabolism|Inborn error]] of [[Inborn errors of carbohydrate metabolism|carbohydrate metabolism]]: [[monosaccharide]] metabolism disorders (including [[glycogen storage disease]]s) ([[ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases#(E73–E74) Carbohydrates|E73-74]], [[List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders#Disorders of carbohydrate transport and metabolism|271]]) |
| state = {{{state|autocollapse}}} | | state = {{{state|autocollapse}}} | ||
| titlestyle = background:Silver | | titlestyle = background:Silver | ||
| − | | group1 = [[Sucrose]], transport< | + | | group1 = [[Sucrose]], transport<br />(extracellular) |
| list1 = {{Navbox subgroup | | list1 = {{Navbox subgroup | ||
| Line 14: | Line 14: | ||
| list3 = [[Glucose-galactose malabsorption]]{{·}} [[Inborn errors of renal tubular transport]] ([[Renal glycosuria]]){{·}} [[Fructose malabsorption]] | | list3 = [[Glucose-galactose malabsorption]]{{·}} [[Inborn errors of renal tubular transport]] ([[Renal glycosuria]]){{·}} [[Fructose malabsorption]] | ||
| − | + | }} | |
| − | }} | ||
| group3 = [[Hexose]] → [[glucose]] | | group3 = [[Hexose]] → [[glucose]] | ||
| Line 21: | Line 20: | ||
| group2 = [[Monosaccharide]] catabolism | | group2 = [[Monosaccharide]] catabolism | ||
| − | | list2 = ''[[fructose]]'': [[Essential fructosuria]]{{·}} [[Hereditary fructose intolerance|Fructose intolerance]]< | + | | list2 = <div>''[[fructose]]'': [[Essential fructosuria]]{{·}} [[Hereditary fructose intolerance|Fructose intolerance]]</div> |
| + | <div>''[[galactose]]/[[galactosemia]] :'' [[Galactokinase deficiency|GALK deficiency]]{{·}} [[Galactose-1-phosphate uridylyltransferase galactosemia|GALT deficiency]]/[[Galactose epimerase deficiency|GALE deficiency]]</div> | ||
| − | + | }} | |
| − | |||
| − | }} | ||
| group4 = [[Glucose]] ⇄ [[glycogen]] | | group4 = [[Glucose]] ⇄ [[glycogen]] | ||
| Line 34: | Line 32: | ||
| group8 = [[Glycogenolysis]] | | group8 = [[Glycogenolysis]] | ||
| − | | list8 = extralysosomal: [[Glycogen storage disease type V|GSD type V, McArdle, muscle glycogen phosphorylase]]/[[Glycogen storage disease type VI|GSD type VI, Hers', liver glycogen phosphorylase]]{{·}} [[Glycogen storage disease type III|GSD type III, Cori's, debranching]]< | + | | list8 = <div>extralysosomal: [[Glycogen storage disease type V|GSD type V, McArdle, muscle glycogen phosphorylase]]/[[Glycogen storage disease type VI|GSD type VI, Hers', liver glycogen phosphorylase]]{{·}} [[Glycogen storage disease type III|GSD type III, Cori's, debranching]]</div> |
| − | + | <div>[[Lysosome|lysosomal]]/[[Lysosomal storage disease|LSD]]: [[Glycogen storage disease type II|GSD type II, Pompe's, glucosidase]]</div> | |
| − | [[Lysosome|lysosomal]]/[[Lysosomal storage disease|LSD]]: [[Glycogen storage disease type II|GSD type II, Pompe's, glucosidase]] | ||
| − | }} | + | }} |
| group7 = [[Glucose]] ⇄ [[Citric acid cycle|CAC]] | | group7 = [[Glucose]] ⇄ [[Citric acid cycle|CAC]] | ||
| Line 44: | Line 41: | ||
| group1 = [[Glycolysis]] | | group1 = [[Glycolysis]] | ||
| − | | list1 = [[MODY 2]]/[[Hyperinsulinemic hypoglycemia|HHF3]]{{·}} [[Phosphofructokinase deficiency|GSD type VII, Tarui's, phosphofructokinase]]{{·}} [[Triosephosphate isomerase deficiency]]{{·}} [[Pyruvate kinase deficiency]] | + | | list1 = [[MODY 2]]/[[Hyperinsulinemic hypoglycemia|HHF3]]{{·}} [[Phosphofructokinase deficiency|GSD type VII, Tarui's, phosphofructokinase]]{{·}} [[Triosephosphate isomerase deficiency]]{{·}} [[Pyruvate kinase deficiency]] |
| group5 = [[Pyruvate]] catabolism | | group5 = [[Pyruvate]] catabolism | ||
| Line 52: | Line 49: | ||
| list6 = [[Pyruvate carboxylase deficiency|PCD]]{{·}} [[Fructose bisphosphatase deficiency]]{{·}} [[Glycogen storage disease type I|GSD type I, von Gierke, glucose 6-phosphatase]] | | list6 = [[Pyruvate carboxylase deficiency|PCD]]{{·}} [[Fructose bisphosphatase deficiency]]{{·}} [[Glycogen storage disease type I|GSD type I, von Gierke, glucose 6-phosphatase]] | ||
| + | }} | ||
| − | + | | group9 = [[Pentose phosphate pathway]] | |
| − | + | | list9 = [[Glucose-6-phosphate dehydrogenase deficiency]]{{·}} [[Pentosuria]] | |
| − | |||
| − | | group9 = [[Pentose phosphate pathway]] | ||
| − | | list9 = [[Glucose-6-phosphate dehydrogenase deficiency]]{{·}} [[Pentosuria]] | ||
| group10 = Other | | group10 = Other | ||
| list10 = [[Hyperoxaluria]] ([[Primary hyperoxaluria]]) | | list10 = [[Hyperoxaluria]] ([[Primary hyperoxaluria]]) | ||
| − | + | | belowstyle = padding:0px; | |
| below = {{Metabolic navs}} | | below = {{Metabolic navs}} | ||
| − | }}<noinclude>[[Category:Inborn errors of metabolism]][[Category:Metabolic disorder templates|{{PAGENAME}}]]</noinclude> | + | }}<noinclude> |
| + | [[Category:Inborn errors of metabolism]] | ||
| + | [[Category:Metabolic disorder templates|{{PAGENAME}}]] | ||
| + | </noinclude> | ||