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 = [[ | + | |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 | ||