Difference between revisions of "Template:Chromosomal abnormalities"
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{{Navbox | {{Navbox | ||
| − | | name | + | | name = Chromosomal abnormalities |
| − | | title = [[ | + | | title = [[Chromosome abnormality|Chromosome abnormalities]] |
| − | | | + | | state = {{{state<includeonly>|autocollapse</includeonly>}}} |
| − | | | + | | listclass = hlist |
| − | | group1 = [[Autosomal | + | | group1 = [[Autosome|Autosomal]] |
| − | | | + | | list1 = {{Navbox|child |
| − | | | + | | group1 = [[Trisomy|Trisomies]]/Tetrasomies |
| − | | | + | | list1 = |
| − | [[ | + | * [[Down syndrome]] |
| + | ** [[Chromosome 21|21]] | ||
| + | * [[Edwards syndrome]] | ||
| + | ** [[Chromosome 18|18]] | ||
| + | * [[Patau syndrome]] | ||
| + | ** [[Chromosome 13|13]] | ||
| − | + | * [[Trisomy 9]] | |
| − | + | * [[Tetrasomy 9p]] | |
| − | [[ | + | * [[Trisomy 8|Warkany syndrome 2]] |
| + | ** [[Chromosome 8|8]] | ||
| + | * [[Cat eye syndrome]]/[[Trisomy 22]] | ||
| + | ** [[Chromosome 22|22]] | ||
| + | * [[Trisomy 16]] | ||
| − | | | + | | group2 = [[Monosomy|Monosomies]]/[[Deletion (genetics)|deletions]] |
| − | | | + | | 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]] | ||
| − | |||
| − | |||
}}<noinclude> | }}<noinclude> | ||
| − | [[Category: | + | {{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}}
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.