Difference between revisions of "Template:Chromosomal abnormalities"

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{{Navbox
 
{{Navbox
| name = Chromosomal abnormalities
+
| name = Chromosomal abnormalities
| title = [[Pathology]]: [[chromosome abnormalities]] ([[ICD-10_Chapter_Q#Q90-Q99_-_Chromosomal_abnormalities.2C_not_elsewhere_classified|Q90-Q99]], [[List_of_ICD-9_codes_740-759:_Congenital_anomalies#Other|758]])
+
| title = [[Chromosome abnormality|Chromosome abnormalities]]
  | titlestyle = background:Silver
+
  | state = {{{state<includeonly>|autocollapse</includeonly>}}}
| groupstyle = background-color: LightGray
+
| listclass = hlist
  
| group1 = [[Autosomal]] [[Trisomy|trisomies]]
+
| group1 = [[Autosome|Autosomal]]
| list1 = [[Down syndrome]] (21), [[Edwards syndrome]] (18), [[Patau syndrome]] (13), [[Trisomy 9]], [[Warkany syndrome 2]] (8), [[Cat eye syndrome]] (22), [[Trisomy 22]], [[Trisomy 16]]
+
| list1 = {{Navbox|child
  
| group2 = [[Autosomal]] [[Monosomy|monosomies]]/[[Deletion (genetics)|deletions]]
+
  | group1 = [[Trisomy|Trisomies]]/Tetrasomies
| list2 = [[Wolf-Hirschhorn syndrome]] (4), [[Cri du chat]] (5), [[Angelman syndrome]]/[[Prader-Willi syndrome]] (15), <br>
+
  | list1 =
[[Miller-Dieker syndrome]]/[[Smith-Magenis syndrome]] (17), [[22q11.2 deletion syndrome]] (22)
+
* [[Down syndrome]]
 +
** [[Chromosome 21|21]]
 +
* [[Edwards syndrome]]
 +
** [[Chromosome 18|18]]
 +
* [[Patau syndrome]]
 +
** [[Chromosome 13|13]]
  
| group3 = [[X chromosome|X]]/[[Y chromosome|Y]] linked
+
* [[Trisomy 9]]
|  list3 = [[Monosomy]]: [[Turner syndrome|Turner syndrome (XO)]]<BR>
+
* [[Tetrasomy 9p]]
[[Trisomy]]: [[Triple X syndrome|Triple X syndrome (XXX)]], [[Klinefelter's syndrome|Klinefelter's syndrome (XXY)]], [[XYY syndrome|XYY]]
+
* [[Trisomy 8|Warkany syndrome 2]]
 +
** [[Chromosome 8|8]]
 +
* [[Cat eye syndrome]]/[[Trisomy 22]]
 +
** [[Chromosome 22|22]]
 +
* [[Trisomy 16]]
  
| group4 = [[chromosomal translocation|Translocations]]
+
  | group2 = [[Monosomy|Monosomies]]/[[Deletion (genetics)|deletions]]
| list4 = [[Philadelphia chromosome]], [[Burkitt's lymphoma]]
+
  | list2 =
 +
* ([[1q21.1 deletion syndrome]]/[[1q21.1 duplication syndrome]]/[[TAR syndrome]]/[[1p36 deletion syndrome]])
 +
** [[Chromosome 1|1]]
 +
* [[Wolf–Hirschhorn syndrome]]
 +
** [[Chromosome 4|4]]
 +
* [[Cri du chat syndrome]]/[[Chromosome 5q deletion syndrome]]
 +
** [[Chromosome 5|5]]
 +
* [[Williams syndrome]]
 +
** [[Chromosome 7|7]]
 +
* [[Jacobsen syndrome]]
 +
** [[Chromosome 11|11]]
 +
* [[Miller–Dieker syndrome]]/[[Smith–Magenis syndrome]]
 +
** [[Chromosome 17|17]]
 +
* [[DiGeorge syndrome]]
 +
** [[Chromosome 22|22]]
 +
* [[22q11.2 distal deletion syndrome]]
 +
** [[Chromosome 22|22]]
 +
* [[22q13 deletion syndrome]]
 +
** [[Chromosome 22|22]]
 +
 
 +
* ''[[genomic imprinting]]''
 +
** [[Angelman syndrome]]/[[Prader–Willi syndrome]] ([[Chromosome 15|15]])
 +
 
 +
* [[Distal 18q-]]/[[Proximal 18q-]]
 +
 
 +
}}
 +
 
 +
| group2 = [[X chromosome|X]]/[[Y chromosome|Y]] linked
 +
| list2 = {{Navbox|child
 +
 
 +
  | group1 = [[Monosomy]]
 +
  | list1 =
 +
* [[Turner syndrome|Turner syndrome (45,X)]]
 +
 
 +
  | group2 = [[Trisomy]]/[[tetrasomy]],<br />[[Aneuploidy|other karyotypes]]/[[Mosaic (genetics)|mosaics]]
 +
  | list2 =
 +
* [[Klinefelter syndrome|Klinefelter syndrome (47,XXY)]]
 +
* [[XXYY syndrome|XXYY syndrome (48,XXYY)]]
 +
* [[XXXY syndrome|XXXY syndrome (48,XXXY)]]
 +
* [[49,XXXYY|49,XXXYY]]
 +
* [[49,XXXXY]]
 +
 
 +
* [[Triple X syndrome|Triple X syndrome (47,XXX)]]
 +
* [[Tetrasomy X|Tetrasomy X (48,XXXX)]]
 +
* [[Pentasomy X|49,XXXXX]]
 +
 
 +
* [[XYY syndrome|Jacobs syndrome (47,XYY)]]
 +
* [[48,XYYY|48,XYYY]]
 +
* [[49,XYYYY|49,XYYYY]]
 +
 
 +
* [[45,X/46,XY mosaicism|45,X/46,XY]]
 +
* [[46,XX/46,XY]]
 +
 
 +
}}
 +
 
 +
| group3 = [[Chromosomal translocation|Translocations]]
 +
| list3 = {{Navbox|child
 +
 
 +
  | group1 = [[Leukemia]]/[[lymphoma]]
 +
  | list1 = {{Navbox|child
 +
 
 +
    | group1 = Lymphoid
 +
    | list1 =
 +
* [[Burkitt's lymphoma]] t(8 [[Myc|MYC]];14 [[IGH@|IGH]])
 +
* [[Follicular lymphoma]] t(14 [[IGH@|IGH]];18 [[Bcl-2|BCL2]])
 +
* [[Mantle cell lymphoma]]/[[Multiple myeloma]] t(11 [[Cyclin D1|CCND1]]:14 [[IGH@|IGH]])
 +
* [[Anaplastic large-cell lymphoma ]] t(2 [[Anaplastic lymphoma kinase|ALK]];5 [[NPM1]])
 +
* [[Acute lymphoblastic leukemia]]
 +
 
 +
    | group2 = Myeloid
 +
    | list2 =
 +
* [[Philadelphia chromosome]] t(9 [[ABL (gene)|ABL]]; 22 [[BCR (gene)|BCR]])
 +
* [[Acute myeloblastic leukemia with maturation]] t(8 [[RUNX1T1]];21 [[RUNX1]])
 +
* [[Acute promyelocytic leukemia]] t(15 [[Promyelocytic leukemia protein|PML]],17 [[Retinoic acid receptor alpha|RARA]])
 +
* [[Acute megakaryoblastic leukemia]] t(1 [[RBM15]];22 [[MKL1]])
 +
 
 +
  }}
 +
 
 +
  | group2 = Other
 +
  | list2 =
 +
* [[Ewing's sarcoma]] t(11 [[FLI1]]; 22 [[Ewing sarcoma breakpoint region 1|EWS]])
 +
* [[Synovial sarcoma]] t(x [[SYT1|SYT]];18 [[Synovial sarcoma, X breakpoint|SSX]])
 +
* [[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]])
 +
* [[Desmoplastic small-round-cell tumor]] t(11 [[WT1]]; 22 [[Ewing sarcoma breakpoint region 1|EWS]])
 +
* [[Alveolar rhabdomyosarcoma]] t(2 [[PAX3]]; 13 [[FOXO1]]) t (1 [[PAX7]]; 13 [[FOXO1]])
 +
 
 +
}}
 +
 
 +
| group4 = Other
 +
| list4 =
 +
* [[Fragile X syndrome]]
 +
* [[Uniparental disomy]]
 +
* [[XX male syndrome]]/[[46,XX testicular disorders of sex development]]
 +
* [[Marker chromosome]]
 +
* [[Ring chromosome]]
 +
** [[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]]
  
| group5 = Other
 
|  list5 = [[Fragile X syndrome]], [[Gonadal dysgenesis]] ([[Mixed gonadal dysgenesis]])
 
 
}}<noinclude>
 
}}<noinclude>
[[Category:Diseases and disorders navigational boxes|{{PAGENAME}}]]
+
{{collapsible option}}
 +
[[Category:Genetic disease and disorder templates by mechanism]]
 
</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.