Difference between revisions of "Template:Cytoskeletal defects"
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imported>DePiep m (rm Mednav index templates. See talk (via AWB script)) |
imported>Colonies Chris |
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| Line 27: | Line 27: | ||
* [[Freeman–Sheldon syndrome]] | * [[Freeman–Sheldon syndrome]] | ||
* [[Nonsyndromic deafness|DFN A3, 4, 11, 17, 22; B2, 30, 37, 48]] | * [[Nonsyndromic deafness|DFN A3, 4, 11, 17, 22; B2, 30, 37, 48]] | ||
| − | * [[ | + | * [[May–Hegglin anomaly]] |
| group4 = [[Troponin]] | | group4 = [[Troponin]] | ||
| Line 48: | Line 48: | ||
* [[Fibrillin]] | * [[Fibrillin]] | ||
** [[Marfan syndrome]] | ** [[Marfan syndrome]] | ||
| − | ** [[ | + | ** [[Weill–Marchesani syndrome]] |
* [[Filamin]] | * [[Filamin]] | ||
** [[FG syndrome|FG syndrome 2]] | ** [[FG syndrome|FG syndrome 2]] | ||
| Line 101: | Line 101: | ||
** [[Mandibuloacral dysplasia]] | ** [[Mandibuloacral dysplasia]] | ||
** [[Dunnigan familial partial lipodystrophy|Dunnigan]] [[Familial partial lipodystrophy]] | ** [[Dunnigan familial partial lipodystrophy|Dunnigan]] [[Familial partial lipodystrophy]] | ||
| − | ** [[ | + | ** [[Emery–Dreifuss muscular dystrophy 2]] |
** [[Limb-girdle muscular dystrophy|Limb-girdle muscular dystrophy 1B]] | ** [[Limb-girdle muscular dystrophy|Limb-girdle muscular dystrophy 1B]] | ||
| − | ** [[ | + | ** [[Charcot–Marie–Tooth disease 2B1]] |
* LMNB | * LMNB | ||
** [[Barraquer–Simons syndrome]] | ** [[Barraquer–Simons syndrome]] | ||
| Line 110: | Line 110: | ||
** [[Osteopoikilosis]] | ** [[Osteopoikilosis]] | ||
* LBR | * LBR | ||
| − | ** [[ | + | ** [[Pelger–Huet anomaly]] |
** [[Hydrops-ectopic calcification-moth-eaten skeletal dysplasia]] | ** [[Hydrops-ectopic calcification-moth-eaten skeletal dysplasia]] | ||
}} | }} | ||
| Line 125: | Line 125: | ||
| list2 = | | list2 = | ||
* [[Primary ciliary dyskinesia]] | * [[Primary ciliary dyskinesia]] | ||
| − | * [[ | + | * [[Short rib-polydactyly syndrome 3]] |
| − | * [[ | + | * [[Asphyxiating thoracic dysplasia 3]] |
| group3 = Other | | group3 = Other | ||
| Line 136: | Line 136: | ||
| group4 = [[Membrane protein|Membrane]] | | group4 = [[Membrane protein|Membrane]] | ||
| list4 = | | list4 = | ||
| − | * [[Spectrin]]: [[ | + | * [[Spectrin]]: [[Spinocerebellar ataxia 5]] |
| − | * [[ | + | * [[Hereditary spherocytosis 2, 3]] |
| − | * [[ | + | * [[Hereditary elliptocytosis 2, 3]] |
| − | [[Ankyrin]]: [[ | + | [[Ankyrin]]: [[Long QT syndrome 4]] |
| − | * [[ | + | * [[Hereditary spherocytosis 1]] |
| group5 = [[Catenin]] | | group5 = [[Catenin]] | ||
Latest revision as of 17:20, 9 March 2017
Initial visibility: currently defaults to autocollapse
To set this template's initial visibility, the |state= parameter may be used:
|state=collapsed:{{Cytoskeletal defects|state=collapsed}}to show the template collapsed, i.e., hidden apart from its title bar|state=expanded:{{Cytoskeletal defects|state=expanded}}to show the template expanded, i.e., fully visible|state=autocollapse:{{Cytoskeletal defects|state=autocollapse}}
If the |state= parameter in the template on this page is not set, the template's initial visibility is taken from the |default= parameter in the Collapsible option template. For the template on this page, that currently evaluates to autocollapse.