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 = 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 <br/> Including [[glycogen storage disease]]s (GSD)
| state = {{{state|autocollapse}}}
+
| state = {{{state<includeonly>|autocollapse</includeonly>}}}
| titlestyle = background:Silver
+
| listclass = hlist
  
| group1 = [[Sucrose]], transport<br />(extracellular)
+
| group1 = [[Sucrose]], transport<br />(extracellular)
| list1 = {{Navbox subgroup
+
| list1 = {{Navbox|child
  
| group1 = [[Disaccharide]] catabolism
+
  | group1 = [[Disaccharide]] catabolism
| list1 = [[Lactose intolerance]]{{·}} [[Sucrose intolerance]]
+
  | list1 =
 +
* [[Lactose intolerance|Congenital alactasia]]
 +
* [[Sucrose intolerance]]
  
| group3 = [[Monosaccharide]] transport
+
  | group2 = [[Monosaccharide]] transport
| list3 = [[Glucose-galactose malabsorption]]{{·}} [[Inborn errors of renal tubular transport]] ([[Renal glycosuria]]){{·}} [[Fructose malabsorption]]
+
  | list2 =
 +
* [[Glucose-galactose malabsorption]]
 +
* [[Inborn errors of renal tubular transport]] ([[Renal glycosuria]])
 +
* [[Fructose malabsorption]]
  
}}
+
}}
  
| group3 = [[Hexose]] → [[glucose]]
+
| group2 = [[Hexose]] → [[glucose]]
| list3 = {{Navbox subgroup
+
| list2 = {{Navbox|child
  
| group2 = [[Monosaccharide]] catabolism
+
  | group1 = [[Monosaccharide]] catabolism
| list2 = <div>''[[fructose]]'': [[Essential fructosuria]]{{·}} [[Hereditary fructose intolerance|Fructose intolerance]]</div>
+
  | list1 = {{Navbox|child
<div>''[[galactose]]/[[galactosemia]] :'' [[Galactokinase deficiency|GALK deficiency]]{{·}} [[Galactose-1-phosphate uridylyltransferase galactosemia|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]]
+
| group3 = [[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>
+
| list3 = {{Navbox|child
<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 deficiency)
 +
* [[Glycogen storage disease type IV|GSD type IV]] (Andersen's disease, branching enzyme deficiency)
 +
* [[Adult polyglucosan body disease]] (APBD)
  
| group7 = [[Glucose]] ⇄ [[Citric acid cycle|CAC]]
+
  | group2 = [[Glycogenolysis]]
| list7 = {{Navbox subgroup
+
  | list2 = {{Navbox|child
 +
    | evenodd = swap
  
| group1 = [[Glycolysis]]
+
    | group1 = {{nobold|Extralysosomal:}}
| list1 = [[MODY 2]]/[[Hyperinsulinemic hypoglycemia|HHF3]]{{·}} [[Phosphofructokinase deficiency|GSD type VII, Tarui's, phosphofructokinase]]{{·}} [[Triosephosphate isomerase deficiency]]{{·}} [[Pyruvate kinase deficiency]]
+
    | 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)
  
| group6 = [[Gluconeogenesis]]
+
    | group2 = {{nobold|[[Lysosome|Lysosomal]] ([[Lysosomal storage disease|LSD]]):}}  
| list6 = [[Pyruvate carboxylase deficiency|PCD]]{{·}} [[Fructose bisphosphatase deficiency]]{{·}} [[Glycogen storage disease type I|GSD type I, von Gierke, glucose 6-phosphatase]]
+
    | list2 =
 +
* [[Glycogen storage disease type II|GSD type II]] (Pompe's disease, glucosidase deficiency)
  
}}
+
  }}
 +
}}
  
| group9 = [[Pentose phosphate pathway]]
+
| group4 = [[Glucose]] [[Citric acid cycle|CAC]]
|  list9 = [[Glucose-6-phosphate dehydrogenase deficiency]]{{·}} [[Transaldolase deficiency]]
+
| list4 = {{Navbox|child
 +
  | evenodd = swap
  
| group10 = Other
+
  | group1 = [[Glycolysis]]
| list10 = [[Hyperoxaluria]] ([[Primary hyperoxaluria]]){{·}} [[Pentosuria]]
+
  | 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]]
  
| belowstyle = background: transparent; padding: 0px;
 
| below = {{Metabolic navs}}
 
 
}}<noinclude>
 
}}<noinclude>
[[Category:Inborn errors of carbohydrate metabolism]]
+
{{collapsible option}}
[[Category:Metabolic disorder templates|{{PAGENAME}}]]
+
[[Category:Metabolic disorder templates]]
 
</noinclude>
 
</noinclude>

Latest revision as of 21:28, 13 August 2020

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