Difference between revisions of "Template:Cytoskeletal defects"

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imported>Arcadian
(Microcephalic osteodysplastic primordial dwarfism type II)
imported>DASHBot
m (Bot:Bypassing redirects in NavBox.)
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{{Navbox
 
{{Navbox
 
|name    = Cytoskeletal defects
 
|name    = Cytoskeletal defects
|title  = [[Cytoskeletal]] defects
+
|title  = [[Cytoskeleton|Cytoskeletal]] defects
 
|image  =  
 
|image  =  
 
|above  =  
 
|above  =  
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}}  
 
}}  
  
|group2  = [[Intermediate filaments|IF]]
+
|group2  = [[intermediate filament|IF]]
 
|list2  = {{Navbox subgroup
 
|list2  = {{Navbox subgroup
  
 
|group1  = 1/2
 
|group1  = 1/2
|list1  = [[Keratin disease|Keratinopathy]] ([[keratosis]], [[keratoderma]], [[hyperkeratosis]]): [[KRT1]] ([[Striate palmoplantar keratoderma|Striate palmoplantar keratoderma 3]], [[Epidermolytic hyperkeratosis]], [[Ichthyosis hystrix|IHCM]]){{·}} [[Keratin 2A|KRT2E]] ([[Ichthyosis bullosa of Siemens]]){{·}} [[KRT3]] ([[Meesmann juvenile epithelial corneal dystrophy]]){{·}} [[KRT4]] ([[White sponge nevus]]){{·}}  [[KRT5]] ([[Epidermolysis bullosa simplex]]){{·}} [[KRT8]] ([[Familial cirrhosis]]){{·}} [[KRT10]] ([[Epidermolytic hyperkeratosis]]){{·}} [[KRT12]] ([[Meesmann juvenile epithelial corneal dystrophy]]){{·}} [[KRT13]] ([[White sponge nevus]]){{·}} [[KRT14]] ([[Epidermolysis bullosa simplex]]){{·}} [[KRT17]] ([[Steatocystoma multiplex]]){{·}} [[KRT18]] ([[Familial cirrhosis]]){{·}} [[KRT81]]/[[KRT83]]/[[KRT86]] ([[Monilethrix]]){{·}} [[Naegeli–Franceschetti–Jadassohn syndrome]]{{·}} [[Reticular pigmented anomaly of the flexures]]
+
|list1  = [[Keratin disease|Keratinopathy]] ([[keratosis]], [[keratoderma]], [[hyperkeratosis]]): [[Keratin 1|KRT1]] ([[Striate palmoplantar keratoderma|Striate palmoplantar keratoderma 3]], [[Epidermolytic hyperkeratosis]], [[Ichthyosis hystrix|IHCM]]){{·}} [[Keratin 2A|KRT2E]] ([[Ichthyosis bullosa of Siemens]]){{·}} [[Keratin 3|KRT3]] ([[Meesmann juvenile epithelial corneal dystrophy]]){{·}} [[Keratin 4|KRT4]] ([[White sponge nevus]]){{·}}  [[Keratin 5|KRT5]] ([[Epidermolysis bullosa simplex]]){{·}} [[Keratin 8|KRT8]] ([[Familial cirrhosis]]){{·}} [[Keratin 10|KRT10]] ([[Epidermolytic hyperkeratosis]]){{·}} [[Keratin 12|KRT12]] ([[Meesmann juvenile epithelial corneal dystrophy]]){{·}} [[Keratin 13|KRT13]] ([[White sponge nevus]]){{·}} [[Keratin 14|KRT14]] ([[Epidermolysis bullosa simplex]]){{·}} [[Keratin 17|KRT17]] ([[Steatocystoma multiplex]]){{·}} [[Keratin 18|KRT18]] ([[Familial cirrhosis]]){{·}} [[KRT81]]/[[KRT83]]/[[KRT86]] ([[Monilethrix]]){{·}} [[Naegeli–Franceschetti–Jadassohn syndrome]]{{·}} [[Reticular pigmented anomaly of the flexures]]
  
 
|group2  = 3
 
|group2  = 3

Revision as of 07:22, 4 March 2011