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 = 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-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
+
| list1 = {{Navbox subgroup
  
| group1 = [[Disaccharide]] catabolism
+
  | group1 = [[Disaccharide]] catabolism
| list1 = [[Lactose intolerance]]{{·}} [[Sucrose intolerance]]
+
  | 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]]
+
  | list3 =
 +
* [[Glucose-galactose malabsorption]]
 +
* [[Inborn errors of renal tubular transport]] ([[Renal glycosuria]])
 +
* [[Fructose malabsorption]]
  
}}
+
}}
  
| group3 = [[Hexose]] → [[glucose]]
+
| group3 = [[Hexose]] → [[glucose]]
| list3 = {{Navbox subgroup
+
| list3 = {{Navbox subgroup
  
| group2 = [[Monosaccharide]] catabolism
+
  | group2 = [[Monosaccharide]] catabolism
| list2 = <div>''[[fructose]]'': [[Essential fructosuria]]{{·}} [[Hereditary fructose intolerance|Fructose intolerance]]</div>
+
  | list2 = {{Navbox subgroup
<div>''[[galactose]]/[[galactosemia]] :'' [[Galactokinase deficiency|GALK deficiency]]{{·}} [[Galactose-1-phosphate uridylyltransferase deficiency|GALT deficiency]]/[[Galactose epimerase deficiency|GALE deficiency]]</div>
 
  
}}
+
      | group1 = {{nobold|[[fructose]]:}}
 +
      | list1 =
 +
* [[Essential fructosuria]]
 +
* [[Hereditary fructose intolerance|Fructose intolerance]]
  
| group4 = [[Glucose]] [[glycogen]]
+
      | group2 = {{nobold|[[galactose]]/[[galactosemia]]:}}
| list4 = {{Navbox subgroup
+
      | list2 =
 +
* [[Galactokinase deficiency|GALK deficiency]]
 +
* [[Galactose-1-phosphate uridylyltransferase deficiency|GALT deficiency]]/[[Galactose epimerase deficiency|GALE deficiency]]
  
| 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]]
+
| group4 = [[Glucose]] [[glycogen]]
|  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>
+
| list4 = {{Navbox subgroup
<div>[[Lysosome|lysosomal]]/[[Lysosomal storage disease|LSD]]: [[Glycogen storage disease type II|GSD type II, Pompe's, glucosidase]]</div>
 
  
}}
+
  | group1 = [[Glycogenesis]]
 +
  | list1 =
 +
* [[Glycogen storage disease type 0|GSD type 0, glycogen synthase]]
 +
* [[Glycogen storage disease type IV|GSD type IV, Andersen's, branching]]
  
| group7 = [[Glucose]] [[Citric acid cycle|CAC]]
+
  | group8 = [[Glycogenolysis]]
| list7 = {{Navbox subgroup
+
  | 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]]
  
| group1 = [[Glycolysis]]
+
  }}
| list1 = [[MODY 2]]/[[Hyperinsulinemic hypoglycemia|HHF3]]{{·}} [[Phosphofructokinase deficiency|GSD type VII, Tarui's, phosphofructokinase]]{{·}} [[Triosephosphate isomerase deficiency]]{{·}} [[Pyruvate kinase deficiency]]
+
  }}
  
| group6 = [[Gluconeogenesis]]
+
| group7 = [[Glucose]] [[Citric acid cycle|CAC]]
|  list6 = [[Pyruvate carboxylase deficiency|PCD]]{{·}} [[Fructose bisphosphatase deficiency]]{{·}} [[Glycogen storage disease type I|GSD type I, von Gierke, glucose 6-phosphatase]]
+
| 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]]
  
| group9 = [[Pentose phosphate pathway]]
+
  | group6 = [[Gluconeogenesis]]
| list9 = [[Glucose-6-phosphate dehydrogenase deficiency]]{{·}} [[Transaldolase deficiency]]
+
  | 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]] ([[Primary hyperoxaluria]]){{·}} [[Pentosuria]]{{·}} [[Aldolase A deficiency]]
+
 
 +
| 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}}
  
| belowstyle = background: transparent; padding: 0px;
 
| below = {{Metabolic navs}}
 
 
}}<noinclude>
 
}}<noinclude>
 
{{collapsible option}}
 
{{collapsible option}}
[[Category:Inborn errors of carbohydrate metabolism]]
+
 
[[Category:Metabolic disorder templates|{{PAGENAME}}]]
+
[[Category:Metabolic disorder templates]]
 
</noinclude>
 
</noinclude>

Revision as of 10:10, 4 December 2013

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