Difference between revisions of "Template:Inborn errors of carbohydrate metabolism"
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imported>NSH002 (switch to horizontal list formatting (see WP:HLIST) + general tidy-up) |
imported>Was a bee m (→top: ICD code exported (from bot request)) |
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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 | + | | title = [[Inborn error of metabolism|Inborn error]] of [[Inborn errors of carbohydrate metabolism|carbohydrate metabolism]]: [[monosaccharide]] metabolism disorders <br/> Including [[glycogen storage disease]]s (GSD) |
| − | | state = {{{state|autocollapse}}} | + | | state = {{{state<includeonly>|autocollapse</includeonly>}}} |
| − | |||
| listclass = hlist | | listclass = hlist | ||
| group1 = [[Sucrose]], transport<br />(extracellular) | | group1 = [[Sucrose]], transport<br />(extracellular) | ||
| − | | list1 = {{Navbox | + | | list1 = {{Navbox|child |
| group1 = [[Disaccharide]] catabolism | | group1 = [[Disaccharide]] catabolism | ||
| list1 = | | list1 = | ||
| − | * [[Lactose intolerance]] | + | * [[Lactose intolerance|Congenital alactasia]] |
* [[Sucrose intolerance]] | * [[Sucrose intolerance]] | ||
| − | | | + | | group2 = [[Monosaccharide]] transport |
| − | | | + | | list2 = |
* [[Glucose-galactose malabsorption]] | * [[Glucose-galactose malabsorption]] | ||
* [[Inborn errors of renal tubular transport]] ([[Renal glycosuria]]) | * [[Inborn errors of renal tubular transport]] ([[Renal glycosuria]]) | ||
| Line 22: | Line 21: | ||
}} | }} | ||
| − | | | + | | group2 = [[Hexose]] → [[glucose]] |
| − | | | + | | list2 = {{Navbox|child |
| − | | | + | | group1 = [[Monosaccharide]] catabolism |
| − | | | + | | list1 = {{Navbox|child |
| − | + | | group1 = {{nobold|[[Fructose]]:}} | |
| − | + | | list1 = | |
* [[Essential fructosuria]] | * [[Essential fructosuria]] | ||
* [[Hereditary fructose intolerance|Fructose intolerance]] | * [[Hereditary fructose intolerance|Fructose intolerance]] | ||
| − | + | | group2 = {{nobold|[[Galactose]] / [[galactosemia]]:}} | |
| − | + | | list2 = | |
* [[Galactokinase deficiency|GALK deficiency]] | * [[Galactokinase deficiency|GALK deficiency]] | ||
* [[Galactose-1-phosphate uridylyltransferase deficiency|GALT deficiency]]/[[Galactose epimerase deficiency|GALE deficiency]] | * [[Galactose-1-phosphate uridylyltransferase deficiency|GALT deficiency]]/[[Galactose epimerase deficiency|GALE deficiency]] | ||
| Line 41: | Line 40: | ||
}} | }} | ||
| − | | | + | | group3 = [[Glucose]] ⇄ [[glycogen]] |
| − | | | + | | list3 = {{Navbox|child |
| group1 = [[Glycogenesis]] | | group1 = [[Glycogenesis]] | ||
| list1 = | | list1 = | ||
| − | * [[Glycogen storage disease type 0|GSD type 0 | + | * [[Glycogen storage disease type 0|GSD type 0]] (glycogen synthase deficiency) |
| − | * [[Glycogen storage disease type IV|GSD type IV | + | * [[Glycogen storage disease type IV|GSD type IV]] (Andersen's disease, branching enzyme deficiency) |
| + | * [[Adult polyglucosan body disease]] (APBD) | ||
| + | |||
| + | | group2 = [[Glycogenolysis]] | ||
| + | | list2 = {{Navbox|child | ||
| + | | evenodd = swap | ||
| + | |||
| + | | group1 = {{nobold|Extralysosomal:}} | ||
| + | | list1 = | ||
| + | * [[Glycogen storage disease type III|GSD type III]] (Cori's disease, debranching enzyme deficiency) | ||
| + | * [[Glycogen storage disease type VI|GSD type VI]] (Hers' disease, liver glycogen phosphorylase deficiency) | ||
| + | * [[Glycogen storage disease type V|GSD type V]] (McArdle's disease, myophosphorylase deficiency) | ||
| + | * [[Glycogen storage disease type IX|GSD type IX]] (phosphorylase kinase deficiency) | ||
| − | + | | group2 = {{nobold|[[Lysosome|Lysosomal]] ([[Lysosomal storage disease|LSD]]):}} | |
| − | |||
| − | |||
| − | | | ||
| − | |||
| − | |||
| − | |||
| list2 = | | list2 = | ||
| − | * | + | * [[Glycogen storage disease type II|GSD type II]] (Pompe's disease, glucosidase deficiency) |
}} | }} | ||
}} | }} | ||
| − | | | + | | group4 = [[Glucose]] ⇄ [[Citric acid cycle|CAC]] |
| − | | | + | | list4 = {{Navbox|child |
| + | | evenodd = swap | ||
| group1 = [[Glycolysis]] | | group1 = [[Glycolysis]] | ||
| list1 = | | list1 = | ||
* [[MODY 2]]/[[Hyperinsulinemic hypoglycemia|HHF3]] | * [[MODY 2]]/[[Hyperinsulinemic hypoglycemia|HHF3]] | ||
| − | * [[Phosphofructokinase deficiency|GSD type VII | + | * [[Phosphofructokinase deficiency|GSD type VII]] (Tarui's disease, phosphofructokinase deficiency) |
* [[Triosephosphate isomerase deficiency]] | * [[Triosephosphate isomerase deficiency]] | ||
* [[Pyruvate kinase deficiency]] | * [[Pyruvate kinase deficiency]] | ||
| − | | | + | | group2 = [[Gluconeogenesis]] |
| − | | | + | | list2 = |
* [[Pyruvate carboxylase deficiency|PCD]] | * [[Pyruvate carboxylase deficiency|PCD]] | ||
* [[Fructose bisphosphatase deficiency]] | * [[Fructose bisphosphatase deficiency]] | ||
| − | * [[Glycogen storage disease type I|GSD type I | + | * [[Glycogen storage disease type I|GSD type I]] (von Gierke's disease, glucose 6-phosphatase deficiency) |
}} | }} | ||
| − | | | + | <!-- group5 omitted to preserve alternating striping --> |
| − | | | + | |
| + | | group6 = [[Pentose phosphate pathway]] | ||
| + | | list6 = | ||
* [[Glucose-6-phosphate dehydrogenase deficiency]] | * [[Glucose-6-phosphate dehydrogenase deficiency]] | ||
* [[Transaldolase deficiency]] | * [[Transaldolase deficiency]] | ||
| + | * [[6-phosphogluconate dehydrogenase deficiency]] | ||
| − | | | + | | group7 = Other |
| − | | | + | | list7 = |
* [[Hyperoxaluria]] | * [[Hyperoxaluria]] | ||
** [[Primary hyperoxaluria]] | ** [[Primary hyperoxaluria]] | ||
* [[Pentosuria]] | * [[Pentosuria]] | ||
* [[Aldolase A deficiency]] | * [[Aldolase A deficiency]] | ||
| − | |||
| − | |||
| − | |||
}}<noinclude> | }}<noinclude> | ||
{{collapsible option}} | {{collapsible option}} | ||
| − | |||
[[Category:Metabolic disorder templates]] | [[Category:Metabolic disorder templates]] | ||
</noinclude> | </noinclude> | ||
Latest revision as of 21:28, 13 August 2020
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.