Difference between revisions of "Template:Chromosomal abnormalities"
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imported>Naraht (remove redirects) |
imported>Was a bee m (→top: ICD code exported (from bot request)) |
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| (4 intermediate revisions by one other user not shown) | |||
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{{Navbox | {{Navbox | ||
| name = Chromosomal abnormalities | | name = Chromosomal abnormalities | ||
| − | | title = [[Chromosome abnormality|Chromosome abnormalities]] | + | | title = [[Chromosome abnormality|Chromosome abnormalities]] |
| state = {{{state<includeonly>|autocollapse</includeonly>}}} | | state = {{{state<includeonly>|autocollapse</includeonly>}}} | ||
| listclass = hlist | | listclass = hlist | ||
| Line 8: | Line 8: | ||
| list1 = {{Navbox|child | | list1 = {{Navbox|child | ||
| − | | group1 = [[Trisomy|Trisomies]] | + | | group1 = [[Trisomy|Trisomies]]/Tetrasomies |
| list1 = | | list1 = | ||
* [[Down syndrome]] | * [[Down syndrome]] | ||
| Line 18: | Line 18: | ||
* [[Trisomy 9]] | * [[Trisomy 9]] | ||
| + | * [[Tetrasomy 9p]] | ||
* [[Trisomy 8|Warkany syndrome 2]] | * [[Trisomy 8|Warkany syndrome 2]] | ||
** [[Chromosome 8|8]] | ** [[Chromosome 8|8]] | ||
| Line 26: | Line 27: | ||
| group2 = [[Monosomy|Monosomies]]/[[Deletion (genetics)|deletions]] | | group2 = [[Monosomy|Monosomies]]/[[Deletion (genetics)|deletions]] | ||
| list2 = | | list2 = | ||
| − | * [[1q21.1 deletion syndrome]]/[[1q21.1 duplication syndrome]]/[[TAR syndrome]] | + | * ([[1q21.1 deletion syndrome]]/[[1q21.1 duplication syndrome]]/[[TAR syndrome]]/[[1p36 deletion syndrome]]) |
** [[Chromosome 1|1]] | ** [[Chromosome 1|1]] | ||
* [[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 66: | ||
* [[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 76: | Line 77: | ||
* [[45,X/46,XY mosaicism|45,X/46,XY]] | * [[45,X/46,XY mosaicism|45,X/46,XY]] | ||
| + | * [[46,XX/46,XY]] | ||
}} | }} | ||
| Line 105: | Line 107: | ||
| 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 122: | ||
* [[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> | ||
Latest revision as of 20:32, 13 August 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.