Difference between revisions of "Template:Chromosomal abnormalities"
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imported>Naraht (remove redirects) |
imported>Naraht (remove redirects) |
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* [[Wolf–Hirschhorn syndrome]] | * [[Wolf–Hirschhorn syndrome]] | ||
** [[Chromosome 4|4]] | ** [[Chromosome 4|4]] | ||
| − | * [[Cri du chat]]/[[Chromosome 5q deletion syndrome]] | + | * [[Cri du chat syndrome]]/[[Chromosome 5q deletion syndrome]] |
** [[Chromosome 5|5]] | ** [[Chromosome 5|5]] | ||
* [[Williams syndrome]] | * [[Williams syndrome]] | ||
| Line 65: | Line 65: | ||
* [[XXXY syndrome|XXXY syndrome (48,XXXY)]] | * [[XXXY syndrome|XXXY syndrome (48,XXXY)]] | ||
* [[49,XXXYY|49,XXXYY]] | * [[49,XXXYY|49,XXXYY]] | ||
| − | * [[ | + | * [[49,XXXXY]] |
* [[Triple X syndrome|Triple X syndrome (47,XXX)]] | * [[Triple X syndrome|Triple X syndrome (47,XXX)]] | ||
* [[Tetrasomy X|Tetrasomy X (48,XXXX)]] | * [[Tetrasomy X|Tetrasomy X (48,XXXX)]] | ||
| − | * [[ | + | * [[Pentasomy X|49,XXXXX]] |
* [[XYY syndrome|Jacobs syndrome (47,XYY)]] | * [[XYY syndrome|Jacobs syndrome (47,XYY)]] | ||
| Line 105: | Line 105: | ||
| list2 = | | list2 = | ||
* [[Ewing's sarcoma]] t(11 [[FLI1]]; 22 [[Ewing sarcoma breakpoint region 1|EWS]]) | * [[Ewing's sarcoma]] t(11 [[FLI1]]; 22 [[Ewing sarcoma breakpoint region 1|EWS]]) | ||
| − | * [[Synovial sarcoma]] t(x [[ | + | * [[Synovial sarcoma]] t(x [[SYT1|SYT]];18 [[Synovial sarcoma, X breakpoint|SSX]]) |
* [[Dermatofibrosarcoma protuberans]] t(17 [[Collagen, type I, alpha 1|COL1A1]];22 [[PDGFB]]) | * [[Dermatofibrosarcoma protuberans]] t(17 [[Collagen, type I, alpha 1|COL1A1]];22 [[PDGFB]]) | ||
* [[Myxoid liposarcoma]] t(12 [[DNA damage-inducible transcript 3|DDIT3]]; 16 [[FUS (gene)|FUS]]) | * [[Myxoid liposarcoma]] t(12 [[DNA damage-inducible transcript 3|DDIT3]]; 16 [[FUS (gene)|FUS]]) | ||
| Line 120: | Line 120: | ||
* [[Marker chromosome]] | * [[Marker chromosome]] | ||
* [[Ring chromosome]] | * [[Ring chromosome]] | ||
| − | ** [[Ring chromosome 6|6]]; [[Ring chromosome 9|9]]; [[Ring chromosome 14 syndrome|14]]; [[Ring chromosome 15|15]]; [[Ring | + | ** [[Ring chromosome 6|6]]; [[Ring chromosome 9|9]]; [[Ring chromosome 14 syndrome|14]]; [[Ring chromosome 15|15]]; [[Ring 18|18]]; [[Ring chromosome 20 syndrome|20]]; [[Ring chromosome 21|21]], [[Ring chromosome 22|22]] |
}}<noinclude> | }}<noinclude> | ||
Revision as of 17:01, 24 January 2020
Initial visibility: currently defaults to autocollapse
To set this template's initial visibility, the |state= parameter may be used:
|state=collapsed:{{Chromosomal abnormalities|state=collapsed}}to show the template collapsed, i.e., hidden apart from its title bar|state=expanded:{{Chromosomal abnormalities|state=expanded}}to show the template expanded, i.e., fully visible|state=autocollapse:{{Chromosomal abnormalities|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.