Indicwiki: 1 revision imported from :alpha:Template:Chromosomal_abnormalities

2023-07-10T13:48:03Z

1 revision imported from alpha:Template:Chromosomal_abnormalities

← Older revision	Revision as of 19:18, 10 July 2023
(No difference)

alpha>Indicwiki: Created page with "{{Navbox | name = Chromosomal abnormalities | title = Chromosome abnormalities | state = {{{state|autocollapse}}} | l..."

2023-03-21T10:17:20Z

Created page with "{{Navbox | name = Chromosomal abnormalities | title = Chromosome abnormalities | state = {{{state<includeonly>|autocollapse</includeonly>}}} | l..."

New page

{{Navbox
| name = Chromosomal abnormalities
| title = [[Chromosome abnormality|Chromosome abnormalities]]
| state = {{{state<includeonly>|autocollapse</includeonly>}}}
| listclass = hlist

| group1 = [[Autosome|Autosomal]]
| list1 = {{Navbox|child

| group1 = [[Trisomy|Trisomies]]/[[Tetrasomy|tetrasomies]]
| list1 =
* [[Patau syndrome]]
** [[Chromosome 13|13]]
* [[Edwards syndrome]]
** [[Chromosome 18|18]]
* [[Down syndrome]]
** [[Chromosome 21|21]]

* [[Trisomy 8|Warkany syndrome 2]]
** [[Chromosome 8|8]]
* [[Trisomy 9]]
* [[Tetrasomy 9p]]
* [[Trisomy 16]]
* [[Cat eye syndrome]]/[[Trisomy 22]]
** [[Chromosome 22|22]]

| group2 = [[Monosomy|Monosomies]]/[[Deletion (genetics)|deletions]]
| list2 =
* ([[1q21.1 copy number variations]]/[[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]]/[[17q12 microdeletion 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|Monosomies]]
| list1 =
* [[Turner syndrome|Turner syndrome (45,X)]]

| group2 = [[Trisomy|Trisomies]]/[[Tetrasomy|tetrasomies]],<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)]]
* [[XXXXY syndrome|XXXXY syndrome (49,XXXXY)]]

* [[Trisomy X|Trisomy X (47,XXX)]]
* [[Tetrasomy X|Tetrasomy X (48,XXXX)]]
* [[Pentasomy X|Pentasomy X (49,XXXXX)]]

* [[XYY syndrome|XYY syndrome (47,XYY)]]
* [[XYYY syndrome|XYYY syndrome (48,XYYY)]]
* [[XYYYY syndrome|XYYYY syndrome (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 lymphoma]] t(8 [[Myc|MYC]];14 [[IGH@|IGH]])
* [[Follicular lymphoma]] t(14 [[IGH@|IGH]];18 [[Bcl-2|BCL2]])
* [[Mantle cell lymphoma]]/[[Multiple myeloma]] [[t(11:14)|t(11 CCND1:14 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 sarcoma]] t(11 [[FLI1]]; 22 [[RNA-binding protein EWS|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 [[RNA-binding protein FUS|FUS]])
* [[Desmoplastic small-round-cell tumor]] t(11 [[Wilms tumor protein|WT1]]; 22 [[RNA-binding protein EWS|EWS]])
* [[Alveolar rhabdomyosarcoma]] t(2 [[PAX3]]; 13 [[Forkhead box protein O1|FOXO1]]) t (1 [[PAX7]]; 13 [[Forkhead box protein O1|FOXO1]])

}}

| group4 = Other
| list4 =
* [[Fragile X syndrome]]
* [[Uniparental disomy]]
* [[XX male syndrome]]/[[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 chromosome 18|18]]; [[Ring chromosome 20 syndrome|20]]; [[Ring chromosome 21|21]], [[Ring chromosome 22|22]]

}}<noinclude>
{{Documentation|content=
{{collapsible option}}

[[Category:Genetic disease and disorder templates by mechanism]]

}}</noinclude>

Template:Chromosomal abnormalities - Revision history

Indicwiki: 1 revision imported from :alpha:Template:Chromosomal_abnormalities

alpha>Indicwiki: Created page with "{{Navbox | name = Chromosomal abnormalities | title = Chromosome abnormalities | state = {{{state|autocollapse}}} | l..."