Indicwiki: 1 revision imported from :alpha:Template:Cytoskeletal_defects

2023-02-23T12:44:21Z

1 revision imported from alpha:Template:Cytoskeletal_defects

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alpha>Indicwiki: Created page with "{{Navbox | name = Cytoskeletal defects | title = Cytoskeletal defects | state = {{{state|autocollapse}}} | bodyclass = hlist | group1 = Mi..."

2023-02-16T06:47:05Z

Created page with "{{Navbox | name = Cytoskeletal defects | title = Cytoskeletal defects | state = {{{state|autocollapse}}} | bodyclass = hlist | group1 = Mi..."

New page

{{Navbox
| name = Cytoskeletal defects
| title = [[Cytoskeleton|Cytoskeletal]] defects
| state = {{{state|autocollapse}}}
| bodyclass = hlist

| group1 = [[Microfilament]]s
| list1 =
{{Navbox|subgroup

| group1 = [[Myofilament]]
| list1 =
{{Navbox|subgroup

| group1 = [[Actin]]
| list1 =
* [[Hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy 11]]
* [[Dilated cardiomyopathy|Dilated cardiomyopathy 1AA]]
* [[Nonsyndromic deafness|DFNA20]]
* [[Nemaline myopathy|Nemaline myopathy 3]]

| 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]]

| group4 = [[Troponin]]
| list4 =
* [[Hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy 7, 2]]
* [[Nemaline myopathy|Nemaline myopathy 4, 5]]

| group5 = [[Tropomyosin]]
| list5 =
* [[Hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy 3]]
* [[Nemaline myopathy|Nemaline myopathy 1]]

| group6 = [[Titin]]
| 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]]
** [[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 2]]
** [[Limb-girdle muscular dystrophy|Limb-girdle muscular dystrophy 1B]]
** [[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 = [[Dynein]]
| list2 =
* [[Primary ciliary dyskinesia]]
* [[Short rib-polydactyly syndrome 3]]
* [[Asphyxiating thoracic dysplasia 3]]

| group3 = Other
| list3 =
* [[Tauopathy]]
* [[Cavernous venous malformation]]
}}

| group4 = [[Membrane protein|Membrane]]
| list4 =
* [[Spectrin]]: [[Spinocerebellar ataxia 5]]
* [[Hereditary spherocytosis 2, 3]]
* [[Hereditary elliptocytosis 2, 3]]

[[Ankyrin]]: [[Long QT syndrome 4]]
* [[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]]: [[Palmoplantar keratoderma|Striate palmoplantar keratoderma 2]]
* [[Palmoplantar keratoderma|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 = ''Related topics: [[Template:Cytoskeletal proteins|Cytoskeletal proteins]]''
}}<noinclude>
{{collapsible option}}
[[Category:Cytoskeletal defects]]
[[Category:Genetic disease and disorder templates by mechanism]]
</noinclude>

Template:Cytoskeletal defects - Revision history

Indicwiki: 1 revision imported from :alpha:Template:Cytoskeletal_defects

alpha>Indicwiki: Created page with "{{Navbox | name = Cytoskeletal defects | title = Cytoskeletal defects | state = {{{state|autocollapse}}} | bodyclass = hlist | group1 = Mi..."