Difference between revisions of "Template:Cytoskeletal defects"
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imported>Arcadian (FG syndrome) |
imported>Frietjes m (WP:HLIST) |
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{{Navbox | {{Navbox | ||
| − | |name | + | | name = Cytoskeletal defects |
| − | |title | + | | title = [[Cytoskeleton|Cytoskeletal]] defects |
| − | | | + | | bodyclass = hlist |
| − | |||
| titlestyle = background:Silver | | titlestyle = background:Silver | ||
| − | |group1 | + | | group1 = [[Microfilament]]s |
| − | |list1 | + | | list1 = |
| − | + | {{Navbox|subgroup | |
| − | |||
| − | |group1 | + | | group1 = [[Myofilament]] |
| − | |list1 | + | | list1 = |
| − | + | {{Navbox|subgroup | |
| − | |||
| − | | group1 = [[Actin]] | + | | group1 = [[Actin]] |
| − | | list1 = [[Hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy 11]] | + | | list1 = |
| + | * [[Hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy 11]] | ||
| + | * [[Dilated cardiomyopathy|Dilated cardiomyopathy 1AA]] | ||
| + | * [[Nonsyndromic deafness|DFNA20]] | ||
| + | * [[Nemaline myopathy|Nemaline myopathy 3]] | ||
| − | |group2 | + | | group2 = [[Myosin]] |
| − | |list2 | + | | 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 | + | | group4 = [[Troponin]] |
| − | |list4 | + | | list4 = |
| + | * [[Hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy 7, 2]] | ||
| + | * [[Nemaline myopathy|Nemaline myopathy 4, 5]] | ||
| − | |group5 | + | | group5 = [[Tropomyosin]] |
| − | |list5 | + | | list5 = |
| + | * [[Hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy 3]] | ||
| + | * [[Nemaline myopathy|Nemaline myopathy 1]] | ||
| − | |group6 | + | | group6 = [[Titin]] |
| − | |list6 | + | | 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]] | ||
| − | + | * [[Peripherin]]: [[Amyotrophic lateral sclerosis]] | |
| − | |||
| − | + | | group3 = 4 | |
| + | | list3 = | ||
| + | * [[Neurofilament]]: [[Parkinson's disease]] | ||
| + | * [[Charcot–Marie–Tooth disease|Charcot–Marie–Tooth disease 1F, 2E]] | ||
| + | * [[Amyotrophic lateral sclerosis]] | ||
| − | | | + | | group4 = 5 |
| − | | | + | | 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]] | ||
| + | }} | ||
| − | | | + | | group3 = [[Microtubule]]s |
| − | + | | list3 = | |
| + | {{Navbox|subgroup | ||
| + | | group1 = [[Kinesin]] | ||
| + | | list1 = | ||
| + | * [[Charcot–Marie–Tooth disease|Charcot–Marie–Tooth disease 2A]] | ||
| + | * [[Hereditary spastic paraplegia|Hereditary spastic paraplegia 10]] | ||
| − | |group2 | + | | group2 = [[Dynein]] |
| − | |list2 | + | | list2 = |
| + | * [[Primary ciliary dyskinesia]] | ||
| + | * [[Short rib-polydactyly syndrome|Short rib-polydactyly syndrome 3]] | ||
| + | * [[Asphyxiating thoracic dysplasia|Asphyxiating thoracic dysplasia 3]] | ||
| − | [[ | + | | group3 = Other |
| + | | list3 = | ||
| + | * [[Tauopathy]] | ||
| + | * [[Cavernous venous malformation]] | ||
| + | }} | ||
| − | [[ | + | | group4 = [[Membrane protein|Membrane]] |
| + | | list4 = | ||
| + | * [[Spectrin]]: [[Spinocerebellar ataxia|Spinocerebellar ataxia 5]] | ||
| + | * [[Hereditary spherocytosis|Hereditary spherocytosis 2, 3]] | ||
| + | * [[Hereditary elliptocytosis|Hereditary elliptocytosis 2, 3]] | ||
| − | + | [[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]]'' {{Protein defects by function navs}} | |
| − | + | }}<noinclude> | |
| − | + | [[Category:Cytoskeletal defects]] | |
| − | + | [[Category:Genetic disease and disorder templates by mechanism]] | |
| − | + | </noinclude> | |
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| − | |below | ||
| − | }}<noinclude>[[Category:Cytoskeletal defects]][[Category:Genetic disease and disorder templates by mechanism | ||