Difference between revisions of "Template:Inborn errors of carbohydrate metabolism"

From blackwiki
Jump to navigation Jump to search
(Blanked the page)
imported>Was a bee
m (→‎top: ICD code exported (from bot request))
 
(18 intermediate revisions by 13 users not shown)
Line 1: Line 1:
 +
{{Navbox
 +
| name = Inborn errors of carbohydrate metabolism
 +
| 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<includeonly>|autocollapse</includeonly>}}}
 +
| listclass = hlist
  
 +
| group1 = [[Sucrose]], transport<br />(extracellular)
 +
| list1 = {{Navbox|child
 +
 +
  | group1 = [[Disaccharide]] catabolism
 +
  | 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 = {{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 =
 +
* [[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>
 +
{{collapsible option}}
 +
[[Category:Metabolic disorder templates]]
 +
</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}}
    • shows the template collapsed to the title bar if there is a {{navbar}}, a {{sidebar}}, or some other table on the page with the collapsible attribute
    • shows the template in its expanded state if there are no other collapsible items on the page

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.