Difference between revisions of "Template:Cytoskeletal defects"

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imported>Arcadian
(FG syndrome)
imported>Frietjes
Line 1: Line 1:
 
{{Navbox
 
{{Navbox
|name   = Cytoskeletal defects
+
| name       = Cytoskeletal defects
|title   = [[Cytoskeleton|Cytoskeletal]] defects
+
| title     = [[Cytoskeleton|Cytoskeletal]] defects
|image  =
+
| bodyclass  = hlist
|above  =  
 
 
| titlestyle = background:Silver
 
| titlestyle = background:Silver
  
|group1 = [[Microfilament]]s
+
| group1 = [[Microfilament]]s
|list1  = {{Navbox subgroup
+
| list1 =
| groupstyle =
+
   {{Navbox|subgroup
| liststyle  =
 
  
|group1 = [[Myofilament]]
+
  | group1 = [[Myofilament]]
|list1   = {{Navbox subgroup
+
  | list1 =
| groupstyle =
+
    {{Navbox|subgroup
| liststyle  =
 
  
| group1 = [[Actin]]
+
    | group1 = [[Actin]]
| list1  = [[Hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy 11]]{{·}} [[Dilated cardiomyopathy|Dilated cardiomyopathy 1AA]]{{·}} [[Nonsyndromic deafness|DFNA20]]{{·}} [[Nemaline myopathy|Nemaline myopathy 3]]
+
    | list1  =  
 +
* [[Hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy 11]]
 +
* [[Dilated cardiomyopathy|Dilated cardiomyopathy 1AA]]
 +
* [[Nonsyndromic deafness|DFNA20]]
 +
* [[Nemaline myopathy|Nemaline myopathy 3]]
  
|group2 = [[Myosin]]
+
    | group2 = [[Myosin]]
|list2   = [[Elejalde syndrome]]{{·}} [[Hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy 1, 8, 10]]{{·}} [[Usher syndrome|Usher syndrome 1B]]{{·}} [[Freeman–Sheldon syndrome]]{{·}} [[Nonsyndromic deafness|DFN A3, 4, 11, 17, 22; B2, 30, 37, 48]]{{·}} [[May-Hegglin anomaly]]
+
    | list2 =  
 +
* [[Elejalde syndrome]]
 +
* [[Hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy 1, 8, 10]]
 +
* [[Usher syndrome|Usher syndrome 1B]]
 +
* [[Freeman–Sheldon syndrome]]
 +
* [[Nonsyndromic deafness|DFN A3, 4, 11, 17, 22; B2, 30, 37, 48]]
 +
* [[May-Hegglin anomaly]]
  
|group4 = [[Troponin]]
+
    | group4 = [[Troponin]]
|list4   = [[Hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy 7, 2]]{{·}} [[Nemaline myopathy|Nemaline myopathy 4, 5]]
+
    | list4 =  
 +
* [[Hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy 7, 2]]
 +
* [[Nemaline myopathy|Nemaline myopathy 4, 5]]
  
|group5 = [[Tropomyosin]]
+
    | group5 = [[Tropomyosin]]
|list5   = [[Hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy 3]]{{·}} [[Nemaline myopathy|Nemaline myopathy 1]]
+
    | list5 =  
 +
* [[Hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy 3]]
 +
* [[Nemaline myopathy|Nemaline myopathy 1]]
  
|group6 = [[Titin]]
+
    | group6 = [[Titin]]
|list6   = [[Hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy 9]]
+
    | list6 =  
 +
* [[Hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy 9]]
 +
  }}
  
 +
  | group2 = Other
 +
  | list2  =
 +
* [[Fibrillin]]
 +
** [[Marfan syndrome]]
 +
** [[Weill-Marchesani syndrome]]
 +
* [[Filamin]]
 +
** [[FG syndrome|FG syndrome 2]]
 +
** [[Boomerang dysplasia]]
 +
** [[Larsen syndrome]]
 +
** [[Terminal osseous dysplasia with pigmentary defects]]
  
 +
  }}
  
 +
| group2 = [[intermediate filament|IF]]
 +
| list2  =
 +
  {{Navbox|subgroup
 +
  | group1 = 1/2
 +
  | 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
 +
  | list2  =
 +
* [[Desmin]]: [[Desmin-related myofibrillar myopathy]]
 +
* [[Dilated cardiomyopathy|Dilated cardiomyopathy 1I]]
  
 +
* [[Glial fibrillary acidic protein|GFAP]]: [[Alexander disease]]
  
|group2  = Other
+
* [[Peripherin]]: [[Amyotrophic lateral sclerosis]]
|list2  = [[Fibrillin]] ([[Marfan syndrome]], [[Weill-Marchesani syndrome]], ){{·}} [[Filamin]] ([[FG syndrome|FG syndrome 2]], [[Boomerang dysplasia]], [[Larsen syndrome]], [[Terminal osseous dysplasia with pigmentary defects]])
 
  
}}
+
  | group3 = 4
 +
  | list3  =
 +
* [[Neurofilament]]: [[Parkinson's disease]]
 +
* [[Charcot–Marie–Tooth disease|Charcot–Marie–Tooth disease 1F, 2E]]
 +
* [[Amyotrophic lateral sclerosis]]
  
|group2 = [[intermediate filament|IF]]
+
  | group4 = 5
|list2   = {{Navbox subgroup
+
  | list4 =  
 +
* [[Laminopathy]]: LMNA
 +
** [[Mandibuloacral dysplasia]]
 +
** [[Dunnigan familial partial lipodystrophy|Dunnigan]] [[Familial partial lipodystrophy]]
 +
** [[Emery-Dreifuss muscular dystrophy|Emery-Dreifuss muscular dystrophy 2]]
 +
** [[Limb-girdle muscular dystrophy|Limb-girdle muscular dystrophy 1B]]
 +
** [[Charcot–Marie–Tooth disease|Charcot–Marie–Tooth disease 2B1]]
 +
* LMNB
 +
** [[Barraquer–Simons syndrome]]
 +
* LEMD3
 +
** [[Buschke–Ollendorff syndrome]]
 +
** [[Osteopoikilosis]]
 +
* LBR
 +
** [[Pelger-Huet anomaly]]
 +
** [[Hydrops-ectopic calcification-moth-eaten skeletal dysplasia]]
 +
   }}
  
|group1  = 1/2
+
| group3 = [[Microtubule]]s
|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]]
+
| list3  =
 +
  {{Navbox|subgroup
 +
  | group1 = [[Kinesin]]
 +
  | list1 =
 +
* [[Charcot–Marie–Tooth disease|Charcot–Marie–Tooth disease 2A]]
 +
* [[Hereditary spastic paraplegia|Hereditary spastic paraplegia 10]]
  
|group2 = 3
+
  | group2 = [[Dynein]]
|list2   = [[Desmin]]: [[Desmin-related myofibrillar myopathy]]{{·}} [[Dilated cardiomyopathy|Dilated cardiomyopathy 1I]]
+
  | list2 =  
 +
* [[Primary ciliary dyskinesia]]
 +
* [[Short rib-polydactyly syndrome|Short rib-polydactyly syndrome 3]]
 +
* [[Asphyxiating thoracic dysplasia|Asphyxiating thoracic dysplasia 3]]
  
[[Glial fibrillary acidic protein|GFAP]]: [[Alexander disease]]
+
  | group3 = Other
 +
  | list3  =
 +
* [[Tauopathy]]
 +
* [[Cavernous venous malformation]]
 +
  }}
  
[[Peripherin]]: [[Amyotrophic lateral sclerosis]]
+
| group4 = [[Membrane protein|Membrane]]
 +
| list4  =
 +
* [[Spectrin]]: [[Spinocerebellar ataxia|Spinocerebellar ataxia 5]]
 +
* [[Hereditary spherocytosis|Hereditary spherocytosis 2, 3]]
 +
* [[Hereditary elliptocytosis|Hereditary elliptocytosis 2, 3]]
  
|group3  = 4
+
[[Ankyrin]]: [[Long QT syndrome|Long QT syndrome 4]]
|list3  = [[Neurofilament]]: [[Parkinson's disease]]{{·}} [[Charcot–Marie–Tooth disease|Charcot–Marie–Tooth disease 1F, 2E]]{{·}} [[Amyotrophic lateral sclerosis]]
+
* [[Hereditary spherocytosis|Hereditary spherocytosis 1]]
  
|group4  = 5
+
| group5 = [[Catenin]]
|list4  = [[Laminopathy]]: LMNA ([[Mandibuloacral dysplasia]], [[Dunnigan familial partial lipodystrophy|Dunnigan]] [[Familial partial lipodystrophy]], [[Emery-Dreifuss muscular dystrophy|Emery-Dreifuss muscular dystrophy 2]], [[Limb-girdle muscular dystrophy|Limb-girdle muscular dystrophy 1B]], [[Charcot–Marie–Tooth disease|Charcot–Marie–Tooth disease 2B1]]){{·}} LMNB ([[Barraquer–Simons syndrome]]){{·}} LEMD3 ([[Buschke–Ollendorff syndrome]], [[Osteopoikilosis]]){{·}} LBR ([[Pelger-Huet anomaly]], [[Hydrops-ectopic calcification-moth-eaten skeletal dysplasia]])
+
| list5  =
 +
* ''[[Adenomatous polyposis coli|APC]]''
 +
** [[Gardner's syndrome]]
 +
** [[Familial adenomatous polyposis]]
 +
* ''[[plakoglobin]]'' ([[Naxos syndrome]])
 +
* ''[[Gigaxonin|GAN]]'' ([[Giant axonal neuropathy]])
  
}}
+
| group6 = Other
 +
| list6  =
 +
* [[desmoplakin]]: [[Striate palmoplantar keratoderma|Striate palmoplantar keratoderma 2]]
 +
* [[Carvajal syndrome]]
 +
* [[Arrhythmogenic right ventricular dysplasia|Arrhythmogenic right ventricular dysplasia 8]]
  
|group3  = [[Microtubule]]s
+
* [[plectin]]: [[Epidermolysis bullosa simplex with muscular dystrophy]]
|list3  = {{Navbox subgroup
+
* [[Epidermolysis bullosa simplex of Ogna]]
  
|group1  = [[Kinesin]]
+
* [[plakophilin]]: [[Skin fragility syndrome]]
|list1  = [[Charcot–Marie–Tooth disease|Charcot–Marie–Tooth disease 2A]]{{·}} [[Hereditary spastic paraplegia|Hereditary spastic paraplegia 10]]
+
* [[Arrhythmogenic right ventricular dysplasia|Arrhythmogenic right ventricular dysplasia 9]]
  
|group2  = [[Dynein]]
+
* [[centrosome]]: ''[[PCNT]]'' ([[Microcephalic osteodysplastic primordial dwarfism type II]])
|list2  = [[Primary ciliary dyskinesia]]{{·}} [[Short rib-polydactyly syndrome|Short rib-polydactyly syndrome 3]]{{·}} [[Asphyxiating thoracic dysplasia|Asphyxiating thoracic dysplasia 3]]
 
  
|group3  = Other
+
| below = ''See also: [[Template:Cytoskeletal proteins|cytoskeletal proteins]]'' {{Protein defects by function navs}}
|list3  = [[Tauopathy]]{{·}} [[Cavernous venous malformation]]
+
}}<noinclude>
 
+
[[Category:Cytoskeletal defects]]
}}
+
[[Category:Genetic disease and disorder templates by mechanism]]
 
+
</noinclude>
|group4  = [[Membrane protein|Membrane]]
 
|list4  = [[Spectrin]]: [[Spinocerebellar ataxia|Spinocerebellar ataxia 5]]{{·}} [[Hereditary spherocytosis|Hereditary spherocytosis 2, 3]]{{·}} [[Hereditary elliptocytosis|Hereditary elliptocytosis 2, 3]]<BR>
 
 
 
[[Ankyrin]]: [[Long QT syndrome|Long QT syndrome 4]]{{·}} [[Hereditary spherocytosis|Hereditary spherocytosis 1]]
 
 
 
|group5  = [[Catenin]]
 
|list5  = ''[[Adenomatous polyposis coli|APC]]'' ([[Gardner's syndrome]], [[Familial adenomatous polyposis]]){{·}} ''[[plakoglobin]]'' ([[Naxos syndrome]]){{·}} ''[[Gigaxonin|GAN]]'' ([[Giant axonal neuropathy]])
 
 
 
|group6  = Other
 
|list6  =
 
 
 
[[desmoplakin]]: [[Striate palmoplantar keratoderma|Striate palmoplantar keratoderma 2]]{{·}} [[Carvajal syndrome]]{{·}} [[Arrhythmogenic right ventricular dysplasia|Arrhythmogenic right ventricular dysplasia 8]]
 
 
 
[[plectin]]: [[Epidermolysis bullosa simplex with muscular dystrophy]]{{·}} [[Epidermolysis bullosa simplex of Ogna]]
 
 
 
[[plakophilin]]: [[Skin fragility syndrome]]{{·}} [[Arrhythmogenic right ventricular dysplasia|Arrhythmogenic right ventricular dysplasia 9]]
 
 
 
[[centrosome]]: ''[[PCNT]]'' ([[Microcephalic osteodysplastic primordial dwarfism type II]])
 
 
 
|below   = ''see also [[Template:Cytoskeletal proteins|cytoskeletal proteins]]''<BR>{{Protein defects by function navs}}
 
}}<noinclude>[[Category:Cytoskeletal defects]][[Category:Genetic disease and disorder templates by mechanism|{{PAGENAME}}]]</noinclude>
 

Revision as of 20:03, 20 September 2012