Difference between revisions of "Template:Chromosomal abnormalities"

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imported>Naraht
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imported>Was a bee
m (→‎top: ICD code exported (from bot request))
 
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{{Navbox
 
{{Navbox
 
  | name = Chromosomal abnormalities
 
  | name = Chromosomal abnormalities
  | title = [[Chromosome abnormality|Chromosome abnormalities]] ([[ICD-10 Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities#Q90–Q99 – Chromosomal abnormalities, not elsewhere classified|Q90–Q99]], [[List of ICD-9 codes 740–759: congenital anomalies#Chromosomal anomalies|758]])
+
  | title = [[Chromosome abnormality|Chromosome abnormalities]]
 
  | state = {{{state<includeonly>|autocollapse</includeonly>}}}
 
  | state = {{{state<includeonly>|autocollapse</includeonly>}}}
 
  | listclass = hlist
 
  | listclass = hlist
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  | 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]]
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* [[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)]]
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* [[45,X/46,XY mosaicism|45,X/46,XY]]
 
* [[45,X/46,XY mosaicism|45,X/46,XY]]
 +
* [[46,XX/46,XY]]
  
 
  }}
 
  }}
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   | 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]])
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* [[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>

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}}
    • 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.