Difference between revisions of "Template:Chromosomal abnormalities"

From blackwiki
Jump to navigation Jump to search
imported>Naraht
(remove redirects)
imported>Naraht
(remove redirects)
Line 30: Line 30:
 
* [[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 syndrome|49,XXXXY]]
+
* [[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)]]
* [[49,XXXXX|49,XXXXX]]
+
* [[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 [[Synaptotagmin 1|SYT]];18 [[Synovial sarcoma, X breakpoint|SSX]])
+
* [[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 chromosome 18|18]]; [[Ring chromosome 20 syndrome|20]]; [[Ring chromosome 21|21]], [[Ring chromosome 22|22]]
+
** [[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}}
    • shows the template collapsed to the title bar if there is a {{navbar}}, a {{sidebar}}, or some other table on the page with the collapsible attribute
    • shows the template in its expanded state if there are no other collapsible items on the page

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.