Difference between revisions of "Template:Chromosomal abnormalities"

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imported>Nicholas0
m (spacing)
imported>Naraht
(remove redirects)
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   | list1 =
 
   | list1 =
 
* [[Down syndrome]]
 
* [[Down syndrome]]
** [[Chromosome 21 (human)|21]]
+
** [[Chromosome 21|21]]
 
* [[Edwards syndrome]]
 
* [[Edwards syndrome]]
** [[Chromosome 18 (human)|18]]
+
** [[Chromosome 18|18]]
 
* [[Patau syndrome]]
 
* [[Patau syndrome]]
** [[Chromosome 13 (human)|13]]
+
** [[Chromosome 13|13]]
  
 
* [[Trisomy 9]]
 
* [[Trisomy 9]]
 
* [[Trisomy 8|Warkany syndrome 2]]
 
* [[Trisomy 8|Warkany syndrome 2]]
** [[Chromosome 8 (human)|8]]
+
** [[Chromosome 8|8]]
 
* [[Cat eye syndrome]]/[[Trisomy 22]]
 
* [[Cat eye syndrome]]/[[Trisomy 22]]
** [[Chromosome 22 (human)|22]]
+
** [[Chromosome 22|22]]
 
* [[Trisomy 16]]
 
* [[Trisomy 16]]
  
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   | list2 =
 
   | list2 =
 
* [[1q21.1 deletion syndrome]]/[[1q21.1 duplication syndrome]]/[[TAR syndrome]]
 
* [[1q21.1 deletion syndrome]]/[[1q21.1 duplication syndrome]]/[[TAR syndrome]]
** [[Chromosome 1 (human)|1]]
+
** [[Chromosome 1|1]]
 
* [[Wolf–Hirschhorn syndrome]]
 
* [[Wolf–Hirschhorn syndrome]]
** [[Chromosome 4 (human)|4]]
+
** [[Chromosome 4|4]]
 
* [[Cri du chat]]/[[Chromosome 5q deletion syndrome]]
 
* [[Cri du chat]]/[[Chromosome 5q deletion syndrome]]
** [[Chromosome 5 (human)|5]]
+
** [[Chromosome 5|5]]
 
* [[Williams syndrome]]
 
* [[Williams syndrome]]
** [[Chromosome 7 (human)|7]]
+
** [[Chromosome 7|7]]
 
* [[Jacobsen syndrome]]
 
* [[Jacobsen syndrome]]
** [[Chromosome 11 (human)|11]]
+
** [[Chromosome 11|11]]
 
* [[Miller–Dieker syndrome]]/[[Smith–Magenis syndrome]]
 
* [[Miller–Dieker syndrome]]/[[Smith–Magenis syndrome]]
** [[Chromosome 17 (human)|17]]
+
** [[Chromosome 17|17]]
 
* [[DiGeorge syndrome]]
 
* [[DiGeorge syndrome]]
** [[Chromosome 22 (human)|22]]
+
** [[Chromosome 22|22]]
 
* [[22q11.2 distal deletion syndrome]]
 
* [[22q11.2 distal deletion syndrome]]
** [[Chromosome 22 (human)|22]]
+
** [[Chromosome 22|22]]
 
* [[22q13 deletion syndrome]]
 
* [[22q13 deletion syndrome]]
** [[Chromosome 22 (human)|22]]
+
** [[Chromosome 22|22]]
  
 
* ''[[genomic imprinting]]''
 
* ''[[genomic imprinting]]''
** [[Angelman syndrome]]/[[Prader–Willi syndrome]] ([[Chromosome 15 (human)|15]])
+
** [[Angelman syndrome]]/[[Prader–Willi syndrome]] ([[Chromosome 15|15]])
  
 
* [[Distal 18q-]]/[[Proximal 18q-]]
 
* [[Distal 18q-]]/[[Proximal 18q-]]

Revision as of 16:59, 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.