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m Maintain {{WPBS}} and vital articles: 3 WikiProject templates. Merge {{VA}} into {{WPBS}}. Keep majority rating "B" in {{WPBS}}. Remove 2 same ratings as {{WPBS}} in {{WikiProject Molecular Biology}}, {{WikiProject Medicine}}.
 
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{{WikiProject Medicine|class=B|importance=High|genetics=yes|nested=yes}}
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{{WikiProject Molecular and Cellular Biology|importance=high|class=B|nested=yes}}
{{WikiProject Medicine |importance=High |genetics=yes}}
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{{Reliable sources for medical articles}}


{{Backwardscopy
==Why are humans so defective compared to other mammals?==
|author = Surhone, L. M., Tennoe, M. T., & Henssonow, S. F.
|year = 2010
|title = Prader-Willi syndrome: Genetic disorder, chromosome 15 (human), chromosome 15q partial deletion, Guido Fanconi, Angelman syndrome, Genomic imprinting, hypotonia
|org = Betascript Publishing
|comments = {{OCLC|727363183}}.
|bot=LivingBot
}}


== Mendelian disorder - no clear definition ==
It would be interesting to see some data and citations on the comparison of humans and other mammals, especially primates in regard to genetic disorders and to see some citations from experts on why this may be, because it is pretty staggering that we humans evolved from stronger, healthier animals yet the human fossil record shows that we have suffered genetic abnormalities for almost our entire tenure on this planet, ie. over 200,000 years. [[User:Proof Reader|Proof Reader]] ([[User talk:Proof Reader|talk]]) 07:21, 1 September 2009 (UTC)


[[Mendelian disorder]] redirects to this article, but it is barely mentioned. It would be good to either stop redirecting or explain properly. [[User:Pgr94|pgr94]] ([[User talk:Pgr94|talk]]) 10:54, 1 June 2016 (UTC)
==Recessive==
[[Recessive disorders]] appears to have been merged into this article in the past.[[User:Leevanjackson|Leevanjackson]] 13:34, 12 August 2006 (UTC)
{{to do}}


== Men? ==
== External links modified ==


Hello fellow Wikipedians,
[[User:82.27.24.198|82.27.24.198]] 09:42, 19 October 2006 (UTC)
:This is not a stupid question. However, one point of clarity is necessary. A disease defined as "fatal" or "lethal" is often deadly in the embryonic stage, so it may not be observed in the population. If such a disease is fatal in ''only'' men or ''only'' women, it is usually because of its locus on the [[sex chromosomes]]. See the section on this page about [[X-linked dominant]] diseases for an example and explanation. - [[User:Raetzsch|Raetzsch]] 19:37, 6 December 2006 (UTC)


I have just modified one external link on [[Genetic disorder]]. Please take a moment to review [https://en.wikipedia.org/w/index.php?diff=prev&oldid=759097150 my edit]. If you have any questions, or need the bot to ignore the links, or the page altogether, please visit [[User:Cyberpower678/FaQs#InternetArchiveBot|this simple FaQ]] for additional information. I made the following changes:
== Polygenic redirection ==
*Added archive https://web.archive.org/web/20080516200040/http://www.health.harvard.edu/diagnostic-tests/amniosentesis.htm to http://www.health.harvard.edu/diagnostic-tests/amniosentesis.htm


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I believe that 'Polygenic' should not redirect here. In its simplest context, the word 'polygenic' describes any phenotypic trait that is attributed to multiple genes. A disease state is not implied. See http://www.medterms.com/script/main/art.asp?articlekey=4986 for a general definition. - [[User:Raetzsch|Raetzsch]] 04:31, 15 November 2006 (UTC)


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== A bombs ==


Cheers.—[[User:InternetArchiveBot|'''<span style="color:darkgrey;font-family:monospace">InternetArchiveBot</span>''']] <span style="color:green;font-family:Rockwell">([[User talk:InternetArchiveBot|Report bug]])</span> 05:43, 9 January 2017 (UTC)
surely it would be better to say that radiation can cause genetic disorders, rather than just mentioning Japan. [[User:Judderman85|Judderman85]] 15:06, 9 December 2006 (UTC)


== Expanison needed ==
== External links modified ==


Hello fellow Wikipedians,
If anyone has any expertise in this area, the article needs some considerable expanding. A section on how chromosome disorders occur, and what can be done about them is needed. Also, the "Study of Genetic Diseases" and "Medical diagnosis, treatment, and counseling" Stubs need expansion.NightFalcon90909 14:35, 7 January 2007 (UTC)


I have just modified one external link on [[Genetic disorder]]. Please take a moment to review [https://en.wikipedia.org/w/index.php?diff=prev&oldid=780413659 my edit]. If you have any questions, or need the bot to ignore the links, or the page altogether, please visit [[User:Cyberpower678/FaQs#InternetArchiveBot|this simple FaQ]] for additional information. I made the following changes:
== Y-linked diseases ==
*Added archive https://web.archive.org/web/20141223183649/https://www.healthxchange.com.sg/News/Pages/Genetic-link-to-4000-diseases.aspx to https://www.healthxchange.com.sg/News/Pages/Genetic-link-to-4000-diseases.aspx
If the only Y-linked disease is infertility, then explain this statement: "All of the sons of an affected father are affected." I highly doubt that infertile men get medical help to produce infertile sons. Or?


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== [[Autosomal recessive]] conditions ==
One new addition to the list is rice-brand earwax, a type of ear excretion that lacks moisture. Please see [[Genetic_disorder#_note-Wade | note #1]] for more info. <small>—The preceding [[Wikipedia:Sign your posts on talk pages|unsigned]] comment was added by [[User:Uniblitz|Uniblitz]] ([[User talk:Uniblitz|talk]] • [[Special:Contributions/Uniblitz|contribs]]) 14:56, 13 May 2007 (UTC).</small><!-- HagermanBot Auto-Unsigned -->


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Is this really called "rice-brand" ear wax? The term seems offensive. <span style="font-size: smaller;" class="autosigned">—Preceding [[Wikipedia:Signatures|unsigned]] comment added by [[Special:Contributions/192.75.139.248|192.75.139.248]] ([[User talk:192.75.139.248|talk]]) 14:40, 2 December 2010 (UTC)</span><!-- Template:UnsignedIP --> <!--Autosigned by SineBot-->


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:I think the correct term is "rice-bran", see [http://www.dizziness-and-balance.com/disorders/hearing/wax2.html] for example. I've changed the article.-<font face="cursive" color="#808080">[[User talk:gadfium|gadfium]]</font> 00:21, 3 December 2010 (UTC)


== Autosomal dominant penetrance ==
== External links modified ==


Hello fellow Wikipedians,
Don't have time to check this out right now - but in the table it mentions most autosomal dom have low penetrance, eg HD. But it looks to me that HD is high penetrance (95%) and I wonder if mostare high penetrance? [[User:Leevanjackson|Leevanjackson]] ([[User talk:Leevanjackson|talk]]) 13:05, 27 November 2007 (UTC)


I have just modified 2 external links on [[Genetic disorder]]. Please take a moment to review [https://en.wikipedia.org/w/index.php?diff=prev&oldid=805044048 my edit]. If you have any questions, or need the bot to ignore the links, or the page altogether, please visit [[User:Cyberpower678/FaQs#InternetArchiveBot|this simple FaQ]] for additional information. I made the following changes:
== Genetic condition vs. genetic disorder ==
*Added archive https://web.archive.org/web/20081216064201/http://rarediseases.info.nih.gov/GARD/ to http://rarediseases.info.nih.gov/GARD/
*Added archive https://web.archive.org/web/20080905105100/http://www.ornl.gov/hgmis/medicine/assist.html to http://www.ornl.gov/hgmis/medicine/assist.html


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Can we change the title of this article to "Genetic condition", which is the term most genetic professionals use? It is more neutral & patient friendly. In [[Wikipedia:Manual of Style (medicine-related articles)#Careful language]], caution on the use of the word "disorder" is advised for this reason.[[User:Kxw1|Kxw1]] ([[User talk:Kxw1|talk]]) 16:58, 19 December 2007 (UTC)


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== Sex-linked disorders? ==


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What would people think about re-organizing the headings to include the X-linked and Y-linked conditions under a more cohesive heading, "Sex-linked disorders"? I know that books use the terms X-linked dominant and X-linked recessive, but these distinctions can be confusing with regard to conditions where the phenotype can be milder in females (example: Ornithine Transcarbamylase deficiency), or when aspects of the phenotype arise in female carriers later in life (example: cardiomyopathy in carriers of Duchenne Muscular Dystrophy mutations).


==Onsets?==
It would be much simpler to handle these all under the same heading and discuss the issues of hemizygosity in males and X-inactivation in females, both of which impact the expression of the X-linked syndromes.
Hello, friends:


So I'm coming here from the genetics task force. While adding more references, do you think it would be a good idea to add onsets of different genetic diseases, or is that a matter for another article?
Any thoughts? [[User:Medical geneticist|Medical geneticist]] ([[User talk:Medical geneticist|talk]]) 22:09, 8 August 2008 (UTC)
:Sounds like a good idea - as it would be more readable to the average person. [[User:Leevanjackson|LeeVJ]] ([[User talk:Leevanjackson|talk]]) 01:34, 9 December 2008 (UTC)


Thank you.
⚫
[[User:Poeticfeelings|Poeticfeelings]] ([[User talk:Poeticfeelings|talk]]) 15:31, 1 July 2019 (UTC)


==Wiki Education assignment: Molecular Genetics==
the X linked recessive bit is wrong i think. if the woman has the condition, and its recessive, then she has 2 (X) copies of the recessive gene. therefore she will give all her sons a copy of the recessive X gene, ie 100% chance the son will have the condition. and similarly her daughters will 100% have at least one copy of the X gene, the other X coming from the father, who may or may not have the condition. or so it seems to me. <span style="font-size: smaller;" class="autosigned">—Preceding [[Wikipedia:Signatures|unsigned]] comment added by [[Special:Contributions/134.36.53.243|134.36.53.243]] ([[User talk:134.36.53.243|talk]]) 14:13, 12 May 2009 (UTC)</span><!-- Template:UnsignedIP --> <!--Autosigned by SineBot-->
{{dashboard.wikiedu.org assignment | course = Wikipedia:Wiki_Ed/Florida_Institute_of_Technology/Molecular_Genetics_(Fall_2022) | assignments = [[User:Sanjana muppavarapu|Sanjana muppavarapu]] | start_date = 2022-08-22 | end_date = 2022-12-09 }}


<span class="wikied-assignment" style="font-size:85%;">— Assignment last updated by [[User:Prabal09|Prabal09]] ([[User talk:Prabal09|talk]]) 17:24, 17 September 2022 (UTC)</span>
:Fixed. This may have been a typo because it looked like the intent was for the example to be a female carrier of an XLR condition. --- [[User:Medical geneticist|Medical geneticist]] ([[User talk:Medical geneticist|talk]]) 16:37, 21 May 2009 (UTC)


== Identification ==
== Epidemiology ==


Where did the following quote come from?
How is DNA used to identify people.
⚫
[[User:THIANYU|THIANYU]] ([[User talk:THIANYU|talk]]) 10:16, 19 February 2009 (UTC)


{{Blockquote
== Klinefleter's symdrome ==
|text=Around 65% of people have some kind of health problem as a result of congenital genetic mutations.
}}


The referenced article https://doi.org/10.4065%2F76.8.777 mentions the following prevalence:
Klinefelter's symdrome is not an X-linked disorder. It is usually caused by non-dysjunction, the genotypic appearance being XXY, or XXXY instead of normal XY.
The only X-linked dorminant disease welknown in humans is Vitamin D Resistant Ricket. <span style="font-size: smaller;" class="autosigned">—Preceding [[Wikipedia:Signatures|unsigned]] comment added by [[Special:Contributions/220.255.7.157|220.255.7.157]] ([[User talk:220.255.7.157|talk]]) 12:57, 21 May 2009 (UTC)</span><!-- Template:UnsignedIP --> <!--Autosigned by SineBot-->
: This passage was a bit misleading so I went ahead and changed it up a bit to clarify. I don't think that the original editor meant to imply that Klinefelter syndrome is X-linked dominant, rather to use it as an example in which a male could be affected with Rett or Aicardi. Hopefully it makes more sense now? I also added your example of XL Rickets which is of course a classic example that should have been there to begin with. --- [[User:Medical geneticist|Medical geneticist]] ([[User talk:Medical geneticist|talk]]) 16:40, 21 May 2009 (UTC)


{{Blockquote
== Monogenic redirection ==
|text=The prevalence of genetic disease ranged from 4.5% to 12% of total admissions. A prevalence of 30% to 40% was documented by Hall et al and Scriver et al by using a broad definition of genetic conditions.
}}


[[User:Uwsi|Uwsi]] ([[User talk:Uwsi|talk]]) 15:42, 27 November 2022 (UTC)
Why does "Monogenic disorder" redirect here? Is it a synonym for "Single gene disorder"? If so, I would specify it somewhere. Like for instance at the beginning of the section "Single gene disorder".<br />
[[Special:Contributions/212.126.224.100|212.126.224.100]] ([[User talk:212.126.224.100|talk]]) 14:02, 22 September 2010 (UTC)

Latest revision as of 12:00, 10 January 2024

Mendelian disorder - no clear definition[edit]

Mendelian disorder redirects to this article, but it is barely mentioned. It would be good to either stop redirecting or explain properly. pgr94 (talk) 10:54, 1 June 2016 (UTC)[reply]

External links modified[edit]

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Onsets?[edit]

Hello, friends:

So I'm coming here from the genetics task force. While adding more references, do you think it would be a good idea to add onsets of different genetic diseases, or is that a matter for another article?

Thank you. Poeticfeelings (talk) 15:31, 1 July 2019 (UTC)[reply]

Wiki Education assignment: Molecular Genetics[edit]

This article was the subject of a Wiki Education Foundation-supported course assignment, between 22 August 2022 and 9 December 2022. Further details are available on the course page. Student editor(s): Sanjana muppavarapu (article contribs).

— Assignment last updated by Prabal09 (talk) 17:24, 17 September 2022 (UTC)[reply]

Epidemiology[edit]

Where did the following quote come from?

Around 65% of people have some kind of health problem as a result of congenital genetic mutations.

The referenced article https://doi.org/10.4065%2F76.8.777 mentions the following prevalence:

The prevalence of genetic disease ranged from 4.5% to 12% of total admissions. A prevalence of 30% to 40% was documented by Hall et al and Scriver et al by using a broad definition of genetic conditions.

Uwsi (talk) 15:42, 27 November 2022 (UTC)[reply]

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