Difference between revisions of "Template:Chromosomal abnormalities"
Jump to navigation
Jump to search
imported>Arcadian (grouping) |
imported>Arcadian (grouping) |
||
| Line 13: | Line 13: | ||
| group2 = [[Monosomy|Monosomies]]/[[Deletion (genetics)|deletions]] | | group2 = [[Monosomy|Monosomies]]/[[Deletion (genetics)|deletions]] | ||
| − | | list2 = [[Wolf-Hirschhorn syndrome]] (4), [[Cri du chat]] (5), [[Williams syndrome]] (7), [[Angelman syndrome]]/[[Prader-Willi syndrome]] (15), <br> | + | | list2 = [[Wolf-Hirschhorn syndrome]] (4), [[Cri du chat]] (5), [[Williams syndrome]] (7), ''[[genomic imprinting]]'' ([[Angelman syndrome]]/[[Prader-Willi syndrome]] (15)), <br> |
[[Miller-Dieker syndrome]]/[[Smith-Magenis syndrome]] (17), [[22q11.2 deletion syndrome]] (22) | [[Miller-Dieker syndrome]]/[[Smith-Magenis syndrome]] (17), [[22q11.2 deletion syndrome]] (22) | ||
| Line 36: | Line 36: | ||
| list4 = [[Philadelphia chromosome]], [[Burkitt's lymphoma]] | | list4 = [[Philadelphia chromosome]], [[Burkitt's lymphoma]] | ||
| − | | group5 = | + | | group5 = [[Gonadal dysgenesis]] |
| − | | list5 = [[ | + | | list5 = [[Mixed gonadal dysgenesis]] |
| + | |||
| + | | group6 = Other | ||
| + | | list6 = [[Fragile X syndrome]], [[Uniparental disomy]] | ||
}}<noinclude> | }}<noinclude> | ||
[[Category:Disease and disorder templates|{{PAGENAME}}]] [[pt:Predefinição:Anomalias cromossômicas]] | [[Category:Disease and disorder templates|{{PAGENAME}}]] [[pt:Predefinição:Anomalias cromossômicas]] | ||
</noinclude> | </noinclude> | ||