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

From blackwiki
Jump to navigation Jump to search
imported>Arcadian
(cat)
imported>Cobaltcigs
Line 1: Line 1:
 
{{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%2C_nutritional_and_metabolic_diseases#.28E73-E74.29_Carbohydrates|E73-74]], [[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|E73-74]], [[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
  
| group1 = [[Sucrose]], transport<BR>(extracellular)
+
| group1 = [[Sucrose]], transport<br />(extracellular)
 
|  list1 = {{Navbox subgroup
 
|  list1 = {{Navbox subgroup
  
Line 14: Line 14:
 
|  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]]
Line 21: Line 20:
  
 
| group2 = [[Monosaccharide]] catabolism
 
| group2 = [[Monosaccharide]] catabolism
|  list2 = ''[[fructose]]'': [[Essential fructosuria]]{{·}} [[Hereditary fructose intolerance|Fructose intolerance]]<BR>
+
|  list2 = <div>''[[fructose]]'': [[Essential fructosuria]]{{·}} [[Hereditary fructose intolerance|Fructose intolerance]]</div>
 +
<div>''[[galactose]]/[[galactosemia]] :'' [[Galactokinase deficiency|GALK deficiency]]{{·}} [[Galactose-1-phosphate uridylyltransferase galactosemia|GALT deficiency]]/[[Galactose epimerase deficiency|GALE deficiency]]</div>
  
''[[galactose]]/[[galactosemia]] :'' [[Galactokinase deficiency|GALK deficiency]]{{·}} [[Galactose-1-phosphate uridylyltransferase galactosemia|GALT deficiency]]/[[Galactose epimerase deficiency|GALE deficiency]]
+
}}
 
 
}}  
 
  
 
| group4 = [[Glucose]] ⇄ [[glycogen]]
 
| group4 = [[Glucose]] ⇄ [[glycogen]]
Line 34: Line 32:
  
 
| group8 = [[Glycogenolysis]]
 
| group8 = [[Glycogenolysis]]
|  list8 = 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]]<BR>
+
|  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>
 
+
<div>[[Lysosome|lysosomal]]/[[Lysosomal storage disease|LSD]]: [[Glycogen storage disease type II|GSD type II, Pompe's, glucosidase]]</div>
[[Lysosome|lysosomal]]/[[Lysosomal storage disease|LSD]]: [[Glycogen storage disease type II|GSD type II, Pompe's, glucosidase]]
 
  
}}  
+
}}
  
 
| group7 = [[Glucose]] ⇄ [[Citric acid cycle|CAC]]
 
| group7 = [[Glucose]] ⇄ [[Citric acid cycle|CAC]]
Line 44: Line 41:
  
 
| group1 = [[Glycolysis]]
 
| group1 = [[Glycolysis]]
| list1  = [[MODY 2]]/[[Hyperinsulinemic hypoglycemia|HHF3]]{{·}} [[Phosphofructokinase deficiency|GSD type VII, Tarui's, phosphofructokinase]]{{·}} [[Triosephosphate isomerase deficiency]]{{·}} [[Pyruvate kinase deficiency]]  
+
| list1  = [[MODY 2]]/[[Hyperinsulinemic hypoglycemia|HHF3]]{{·}} [[Phosphofructokinase deficiency|GSD type VII, Tarui's, phosphofructokinase]]{{·}} [[Triosephosphate isomerase deficiency]]{{·}} [[Pyruvate kinase deficiency]]
  
 
| group5 = [[Pyruvate]] catabolism
 
| group5 = [[Pyruvate]] catabolism
Line 52: Line 49:
 
|  list6 = [[Pyruvate carboxylase deficiency|PCD]]{{·}} [[Fructose bisphosphatase deficiency]]{{·}} [[Glycogen storage disease type I|GSD type I, von Gierke, glucose 6-phosphatase]]
 
|  list6 = [[Pyruvate carboxylase deficiency|PCD]]{{·}} [[Fructose bisphosphatase deficiency]]{{·}} [[Glycogen storage disease type I|GSD type I, von Gierke, glucose 6-phosphatase]]
  
 +
}}
  
 
+
| group9 = [[Pentose phosphate pathway]]
}}
+
|  list9 = [[Glucose-6-phosphate dehydrogenase deficiency]]{{·}} [[Pentosuria]]
 
 
| group9 = [[Pentose phosphate pathway]]
 
|  list9 = [[Glucose-6-phosphate dehydrogenase deficiency]]{{·}} [[Pentosuria]]  
 
  
 
| group10 = Other
 
| group10 = Other
 
| list10 = [[Hyperoxaluria]] ([[Primary hyperoxaluria]])
 
| list10 = [[Hyperoxaluria]] ([[Primary hyperoxaluria]])
  
 
+
| belowstyle = padding:0px;
 
| below = {{Metabolic navs}}
 
| below = {{Metabolic navs}}
}}<noinclude>[[Category:Inborn errors of metabolism]][[Category:Metabolic disorder templates|{{PAGENAME}}]]</noinclude>
+
}}<noinclude>
 +
[[Category:Inborn errors of metabolism]]
 +
[[Category:Metabolic disorder templates|{{PAGENAME}}]]
 +
</noinclude>

Revision as of 23:55, 21 December 2010