Difference between revisions of "Template:Inborn errors of carbohydrate metabolism"
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imported>Arcadian (Transaldolase deficiency) |
imported>Was a bee m (→top: ICD code exported (from bot request)) |
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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 | + | | 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 |
− | | group1 = [[Sucrose]], transport<br />(extracellular) | + | | group1 = [[Sucrose]], transport<br />(extracellular) |
− | | | + | | list1 = {{Navbox|child |
− | | group1 = [[Disaccharide]] catabolism | + | | group1 = [[Disaccharide]] catabolism |
− | | list1 | + | | list1 = |
+ | * [[Lactose intolerance|Congenital alactasia]] | ||
+ | * [[Sucrose intolerance]] | ||
− | | | + | | group2 = [[Monosaccharide]] transport |
− | | | + | | list2 = |
+ | * [[Glucose-galactose malabsorption]] | ||
+ | * [[Inborn errors of renal tubular transport]] ([[Renal glycosuria]]) | ||
+ | * [[Fructose malabsorption]] | ||
− | }} | + | }} |
− | | | + | | group2 = [[Hexose]] → [[glucose]] |
− | | | + | | list2 = {{Navbox|child |
− | | | + | | group1 = [[Monosaccharide]] catabolism |
− | | | + | | list1 = {{Navbox|child |
− | |||
− | }} | + | | 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]] | ||
− | + | }} | |
− | + | }} | |
− | | | + | | group3 = [[Glucose]] ⇄ [[glycogen]] |
− | + | | list3 = {{Navbox|child | |
− | |||
− | + | | group1 = [[Glycogenesis]] | |
+ | | list1 = | ||
+ | * [[Glycogen storage disease type 0|GSD type 0]] (glycogen synthase deficiency) | ||
+ | * [[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 = | + | | group1 = {{nobold|Extralysosomal:}} |
− | | list1 | + | | 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 = |
+ | * [[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]] |
− | | | + | | list1 = |
+ | * [[MODY 2]]/[[Hyperinsulinemic hypoglycemia|HHF3]] | ||
+ | * [[Phosphofructokinase deficiency|GSD type VII]] (Tarui's disease, phosphofructokinase deficiency) | ||
+ | * [[Triosephosphate isomerase deficiency]] | ||
+ | * [[Pyruvate kinase deficiency]] | ||
+ | |||
+ | | group2 = [[Gluconeogenesis]] | ||
+ | | list2 = | ||
+ | * [[Pyruvate carboxylase deficiency|PCD]] | ||
+ | * [[Fructose bisphosphatase deficiency]] | ||
+ | * [[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]] | ||
+ | * [[Transaldolase deficiency]] | ||
+ | * [[6-phosphogluconate dehydrogenase deficiency]] | ||
+ | |||
+ | | group7 = Other | ||
+ | | list7 = | ||
+ | * [[Hyperoxaluria]] | ||
+ | ** [[Primary hyperoxaluria]] | ||
+ | * [[Pentosuria]] | ||
+ | * [[Aldolase A deficiency]] | ||
− | |||
− | |||
}}<noinclude> | }}<noinclude> | ||
− | + | {{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
.