Difference between revisions of "Template:Inborn errors of carbohydrate metabolism"
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imported>Jereiniger |
imported>NSH002 (switch to horizontal list formatting (see WP:HLIST) + general tidy-up) |
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{{Navbox | {{Navbox | ||
| − | | name | + | | 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-10 Chapter IV: Endocrine, nutritional and metabolic diseases#(E73–E74) Carbohydrates|E73–E74]], [[List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders#Disorders of carbohydrate transport and metabolism|271]]) | + | | 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–E74]], [[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 |
| + | | listclass = hlist | ||
| − | | group1 = [[Sucrose]], transport<br />(extracellular) | + | | group1 = [[Sucrose]], transport<br />(extracellular) |
| − | | | + | | list1 = {{Navbox subgroup |
| − | | group1 = [[Disaccharide]] catabolism | + | | group1 = [[Disaccharide]] catabolism |
| − | | list1 | + | | list1 = |
| + | * [[Lactose intolerance]] | ||
| + | * [[Sucrose intolerance]] | ||
| − | | group3 = [[Monosaccharide]] transport | + | | group3 = [[Monosaccharide]] transport |
| − | | | + | | list3 = |
| + | * [[Glucose-galactose malabsorption]] | ||
| + | * [[Inborn errors of renal tubular transport]] ([[Renal glycosuria]]) | ||
| + | * [[Fructose malabsorption]] | ||
| − | }} | + | }} |
| − | | group3 = [[Hexose]] → [[glucose]] | + | | group3 = [[Hexose]] → [[glucose]] |
| − | | | + | | list3 = {{Navbox subgroup |
| − | | group2 = [[Monosaccharide]] catabolism | + | | group2 = [[Monosaccharide]] catabolism |
| − | | | + | | list2 = {{Navbox subgroup |
| − | |||
| − | }} | + | | group1 = {{nobold|[[fructose]]:}} |
| + | | list1 = | ||
| + | * [[Essential fructosuria]] | ||
| + | * [[Hereditary fructose intolerance|Fructose intolerance]] | ||
| − | | | + | | group2 = {{nobold|[[galactose]]/[[galactosemia]]:}} |
| − | | | + | | list2 = |
| + | * [[Galactokinase deficiency|GALK deficiency]] | ||
| + | * [[Galactose-1-phosphate uridylyltransferase deficiency|GALT deficiency]]/[[Galactose epimerase deficiency|GALE deficiency]] | ||
| − | + | }} | |
| − | + | }} | |
| − | | | + | | group4 = [[Glucose]] ⇄ [[glycogen]] |
| − | + | | list4 = {{Navbox subgroup | |
| − | |||
| − | + | | group1 = [[Glycogenesis]] | |
| + | | list1 = | ||
| + | * [[Glycogen storage disease type 0|GSD type 0, glycogen synthase]] | ||
| + | * [[Glycogen storage disease type IV|GSD type IV, Andersen's, branching]] | ||
| − | | | + | | group8 = [[Glycogenolysis]] |
| − | | | + | | list8 = {{Navbox subgroup |
| + | |||
| + | | group1 = {{nobold|extralysosomal:}} | ||
| + | | list1 = | ||
| + | * [[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]] | ||
| + | | list2 = | ||
| + | * [[Lysosome|lysosomal]]/[[Lysosomal storage disease|LSD]]: [[Glycogen storage disease type II|GSD type II, Pompe's, glucosidase]] | ||
| − | + | }} | |
| − | + | }} | |
| − | | | + | | group7 = [[Glucose]] ⇄ [[Citric acid cycle|CAC]] |
| − | + | | list7 = {{Navbox subgroup | |
| − | + | | group1 = [[Glycolysis]] | |
| + | | list1 = | ||
| + | * [[MODY 2]]/[[Hyperinsulinemic hypoglycemia|HHF3]] | ||
| + | * [[Phosphofructokinase deficiency|GSD type VII, Tarui's, phosphofructokinase]] | ||
| + | * [[Triosephosphate isomerase deficiency]] | ||
| + | * [[Pyruvate kinase deficiency]] | ||
| − | | | + | | group6 = [[Gluconeogenesis]] |
| − | | | + | | list6 = |
| + | * [[Pyruvate carboxylase deficiency|PCD]] | ||
| + | * [[Fructose bisphosphatase deficiency]] | ||
| + | * [[Glycogen storage disease type I|GSD type I, von Gierke, glucose 6-phosphatase]] | ||
| − | | group10 = Other | + | }} |
| − | | list10 = [[Hyperoxaluria]] | + | |
| + | | group9 = [[Pentose phosphate pathway]] | ||
| + | | list9 = | ||
| + | * [[Glucose-6-phosphate dehydrogenase deficiency]] | ||
| + | * [[Transaldolase deficiency]] | ||
| + | |||
| + | | group10 = Other | ||
| + | | list10 = | ||
| + | * [[Hyperoxaluria]] | ||
| + | ** [[Primary hyperoxaluria]] | ||
| + | * [[Pentosuria]] | ||
| + | * [[Aldolase A deficiency]] | ||
| + | |||
| + | | belowstyle = background: transparent; padding: 0px; | ||
| + | | below = {{Metabolic navs}} | ||
| − | |||
| − | |||
}}<noinclude> | }}<noinclude> | ||
{{collapsible option}} | {{collapsible option}} | ||
| − | + | ||
| − | [[Category:Metabolic disorder templates | + | [[Category:Metabolic disorder templates]] |
</noinclude> | </noinclude> | ||
Revision as of 10:10, 4 December 2013
Initial visibility: currently defaults to autocollapse
To set this template's initial visibility, the |state= parameter may be used:
|state=collapsed:{{Inborn errors of carbohydrate metabolism|state=collapsed}}to show the template collapsed, i.e., hidden apart from its title bar|state=expanded:{{Inborn errors of carbohydrate metabolism|state=expanded}}to show the template expanded, i.e., fully visible|state=autocollapse:{{Inborn errors of carbohydrate metabolism|state=autocollapse}}
If the |state= parameter in the template on this page is not set, the template's initial visibility is taken from the |default= parameter in the Collapsible option template. For the template on this page, that currently evaluates to autocollapse.