User talk:NotCarlJohnson1992

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Happy editing! Jay8g [VTE] 20:33, 6 January 2025 (UTC)

Speedy deletion nomination of Draf/Combined Saposin Deficiency

A tag has been placed on Draf/Combined Saposin Deficiency requesting that it be speedily deleted from Wikipedia. This has been done under section R3 of the criteria for speedy deletion, because it is a recently created redirect from an implausible typo or misnomer, or other unlikely search term.

If you think this page should not be deleted for this reason, you may contest the nomination by visiting the page and clicking the button labelled "Contest this speedy deletion". This will give you the opportunity to explain why you believe the page should not be deleted. However, be aware that once a page is tagged for speedy deletion, it may be deleted without delay. Please do not remove the speedy deletion tag from the page yourself, but do not hesitate to add information in line with Wikipedia's policies and guidelines. Fram (talk) 15:34, 7 January 2025 (UTC)

I have sent you a note about a page you started

Hi NotCarlJohnson1992. Thank you for your work on Smith-Kingsmore syndrome. Another editor, Klbrain, has reviewed it as part of new pages patrol and left the following comment:

Thanks for helpfully creating this page for a rare disease. I've linked it from mTOR and Wikidata.

To reply, leave a comment here and begin it with {{Re|Klbrain}}. (Message delivered via the Page Curation tool, on behalf of the reviewer.)

Klbrain (talk) 14:57, 16 January 2025 (UTC)

Speedy deletion nomination of Draft/Temple Syndrome

Hello NotCarlJohnson1992,

I wanted to let you know that I just tagged Draft/Temple Syndrome for deletion, because it's a redirect from an article title to a namespace that's not for articles.

If you don't want Draft/Temple Syndrome to be deleted, you can contest this deletion, but don't remove the speedy deletion tag from the top.

You can leave a note on my talk page if you have questions. Thanks!

Message delivered via the Page Curation tool, on behalf of the reviewer.

Adamtt9 (talk) 13:18, 19 January 2025 (UTC)

Speedy deletion nomination of Temple Syndrome

Hello NotCarlJohnson1992,

I wanted to let you know that I just tagged Temple Syndrome for deletion, because it's a redirect from an article title to a namespace that's not for articles.

If you don't want Temple Syndrome to be deleted, you can contest this deletion, but don't remove the speedy deletion tag from the top.

You can leave a note on my talk page if you have questions. Thanks!

Message delivered via the Page Curation tool, on behalf of the reviewer.

Adamtt9 (talk) 15:37, 19 January 2025 (UTC)

I have sent you a note about a page you started

Hi NotCarlJohnson1992. Thank you for your work on CARASAL. Another editor, Klbrain, has reviewed it as part of new pages patrol and left the following comment:

Thanks for creating this page. It seems reasonable to keep this distinct from both Galactosialidosis and the set of CARASIL and CADASIL. For the latter set, perhaps a 'distingush' template might be helpful. There is a Wikidata entry for some of the key papers, but not the disorder; something else for somone to do. The page is appropriately developed and linked (for a rare disorder).

To reply, leave a comment here and begin it with {{Re|Klbrain}}. (Message delivered via the Page Curation tool, on behalf of the reviewer.)

Klbrain (talk) 15:47, 23 February 2025 (UTC)

Your thread has been archived

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Hello NotCarlJohnson1992! The thread you created at the Teahouse, Hello!, has been archived because there was no discussion for a few days.

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See also the help page about the archival process. The archival was done by lowercase sigmabot III, and this notification was delivered by KiranBOT, both automated accounts. You can opt out of future notifications by placing {{bots|deny=KiranBOT}} on top of the current page (your user talk page). —KiranBOT (talk) 03:32, 5 March 2025 (UTC)

Some baklava for you!

Thanks for helpfully creating a page on Schaaf-Yang syndrome. The page looks good! Klbrain (talk) 09:10, 15 March 2025 (UTC)

I have sent you a note about a page you started

Hi NotCarlJohnson1992. Thank you for your work on Mosaic variegated aneuploidy syndrome. Another editor, Klbrain, has reviewed it as part of new pages patrol and left the following comment:

Thanks for creating this page for a this (very) rare disease. Many of the sections are quite short, and can probably be expanded from the existing references. It's also helpful to write prose in an engaging way, which I know can be challenging when discussion technical subjects! Remember that your readership should be principally a lay audience.

To reply, leave a comment here and begin it with {{Re|Klbrain}}. (Message delivered via the Page Curation tool, on behalf of the reviewer.)

Klbrain (talk) 21:37, 28 March 2025 (UTC)

Okay i will try my best to expand it. NotCarlJohnson1992 (talk) 04:28, 29 March 2025 (UTC)
So, I expanded the diagnosis section and I doubt that I can expand the other ones. NotCarlJohnson1992 (talk) 12:52, 29 March 2025 (UTC)

I have sent you a note about a page you started

Hi NotCarlJohnson1992. Thank you for your work on FOXG1 syndrome. Another editor, IntentionallyDense, has reviewed it as part of new pages patrol and left the following comment:

Good to see someone working on the rarer genetic diseases. I would recommend possibly rewording some of the signs and symptoms as I'm not sure the current format is super helpful.

To reply, leave a comment here and begin it with {{Re|IntentionallyDense}}. (Message delivered via the Page Curation tool, on behalf of the reviewer.)

IntentionallyDense (Contribs) 04:30, 24 April 2025 (UTC)

Hello, thank you for reviewing my page that I’ve created.
Also, could you please give me some recommendations about making page better?
@IntentionallyDense NotCarlJohnson1992 (talk) 05:04, 24 April 2025 (UTC)

April 2025

Information icon Thank you for your contributions. It seems that you have added Creative Commons licensed text to one or more Wikipedia articles, such as FOXG1 syndrome. You are welcome to import appropriate Creative Commons licensed content to articles, but in order to meet the Wikipedia guideline on plagiarism, such content must be fully attributed. This requires not only acknowledging the source, but acknowledging that the source is copied. There are several methods to do this described at Wikipedia:Plagiarism#Compatibly licensed sources, including the usage of an attribution template. Please make sure that any Creative Commons content you have already imported is fully attributed. Thank you. — Diannaa 🍁 (talk) 12:58, 28 April 2025 (UTC)

I beg your pardon, I need to insert attribution template into citations? @Diannaa NotCarlJohnson1992 (talk) 13:46, 28 April 2025 (UTC)
Yes. For CC-by-4.0 please use this: {{Creative Commons text attribution notice|cc=by4|from this source=yes}}Diannaa 🍁 (talk) 19:20, 28 April 2025 (UTC)
As far as I see, you added it. Next time, I will make sure to add an attribution template in the article if needed. Thank you! NotCarlJohnson1992 (talk) 19:28, 28 April 2025 (UTC)

I have sent you a note about a page you started

Hi NotCarlJohnson1992. Thank you for your work on Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome. Another editor, Klbrain, has reviewed it as part of new pages patrol and left the following comment:

Thanks for creating a page for this very rare disease. I've linked it through Wikidata (something that can help with data linking and sharing across projects).

To reply, leave a comment here and begin it with {{Re|Klbrain}}. (Message delivered via the Page Curation tool, on behalf of the reviewer.)

Klbrain (talk) 19:03, 5 May 2025 (UTC)

Thank you!

Hello, thank you for thanking me my two edits about a medical condition-related article! Eru719 (talk) 05:42, 2 June 2025 (UTC)

Thank you again for your contributions, because I make typos frequently (unfortunately) and these edits are very helpful.
P.S. I still try to decrease the quantity of typos. NotCarlJohnson1992 (talk) 08:11, 2 June 2025 (UTC)
If you want to correct spellings, just search a misspelled word until there's a Wikipedia article that contains the said misspelled word
Note I do not edit references that have wrong spellings Eru719 (talk) 08:14, 2 June 2025 (UTC)
Okay, I will take your advice.
Thank you! NotCarlJohnson1992 (talk) 08:16, 2 June 2025 (UTC)

Concern regarding Draft:Kagami-Ogata Syndrome

Information icon Hello, NotCarlJohnson1992. This is a bot-delivered message letting you know that Draft:Kagami-Ogata Syndrome, a page you created, has not been edited in at least 5 months. Drafts that have not been edited for six months may be deleted, so if you wish to retain the page, please edit it again or request that it be moved to your userspace.

If the page has already been deleted, you can request it be undeleted so you can continue working on it.

Thank you for your submission to Wikipedia. FireflyBot (talk) 21:08, 6 July 2025 (UTC)

Your draft article, Draft:Combined Saposin Deficiency

Hello, NotCarlJohnson1992. This message concerns the Articles for Creation submission or draft page you started, "Combined Saposin Deficiency".

Drafts that go unedited for six months are eligible for deletion, in accordance with our draftspace policy, and this one has been nominated for deletion. If you plan on working on it further, or editing it to address the issues raised if it was declined, simply edit the submission, and remove the {{db-afc}}, {{db-draft}}, or {{db-g13}} code.

If your submission has already been deleted by the time you read this, you can request its undeletion by following the instructions here. An administrator will, in most cases, restore the draft so you can continue to work on it.

Thank you for your submission to Wikipedia! DreamRimmer bot II (talk) 15:27, 7 July 2025 (UTC)

Your draft article, Draft:Kagami-Ogata Syndrome

Hello, NotCarlJohnson1992. This message concerns the Articles for Creation submission or draft page you started, "Kagami-Ogata Syndrome".

Drafts that go unedited for six months are eligible for deletion, in accordance with our draftspace policy, and this one has been nominated for deletion. If you plan on working on it further, or editing it to address the issues raised if it was declined, simply edit the submission, and remove the {{db-afc}}, {{db-draft}}, or {{db-g13}} code.

If your submission has already been deleted by the time you read this, you can request its undeletion by following the instructions here. An administrator will, in most cases, restore the draft so you can continue to work on it.

Thank you for your submission to Wikipedia! DreamRimmer bot II (talk) 08:26, 19 July 2025 (UTC)

DYK for Meier-Gorlin syndrome

On 31 August 2025, Did you know was updated with a fact from the article Meier-Gorlin syndrome, which you recently created, substantially expanded, or brought to good article status. The fact was ... that as of 2024, fewer than 150 people had ever been diagnosed with Meier-Gorlin syndrome? The nomination discussion and review may be seen at Template:Did you know nominations/Meier-Gorlin syndrome. You are welcome to check how many pageviews the nominated article or articles got while on the front page (here's how, Meier-Gorlin syndrome), and the hook may be added to the statistics page after its run on the Main Page has completed. Finally, if you know of an interesting fact from another recently created article, then please feel free to suggest it on the Did you know talk page.

  Amakuru (talk) 00:02, 31 August 2025 (UTC)

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CS1 error on Beta-propeller protein-associated neurodegeneration

Hello, I'm Qwerfjkl (bot). I have automatically detected that this edit performed by you, on the page Beta-propeller protein-associated neurodegeneration, may have introduced referencing errors. They are as follows:

Please check this page and fix the errors highlighted. If you think this is a false positive, you can report it to my operator. Thanks, Qwerfjkl (bot) (talk) 14:17, 7 January 2026 (UTC)

I have sent you a note about a page you started

Hi NotCarlJohnson1992. Thank you for your work on Coloboma-heart defects-atresia choanae-retardation of growth and development-genitourinary problems-ear abnormalities syndrome. Another editor, Casablanca Rock, has reviewed it as part of new pages patrol and left the following comment:

Verified as alternative name from https://rarediseases.info.nih.gov/diseases/29/charge-syndrome

To reply, leave a comment here and begin it with {{Re|Casablanca Rock}}. (Message delivered via the Page Curation tool, on behalf of the reviewer.)

Casablanca 🪨(T) 03:02, 8 January 2026 (UTC)

DYK for Beta-propeller protein-associated neurodegeneration

On 22 February 2026, Did you know was updated with a fact from the article Beta-propeller protein-associated neurodegeneration, which you recently created, substantially expanded, or brought to good article status. The fact was ... that beta-propeller protein-associated neurodegeneration can mostly be seen in girls due to its inheritance nature? The nomination discussion and review may be seen at Template:Did you know nominations/Beta-propeller protein-associated neurodegeneration. You are welcome to check how many pageviews the nominated article or articles got while on the front page (here's how, Beta-propeller protein-associated neurodegeneration), and the hook may be added to the statistics page after its run on the Main Page has completed. Finally, if you know of an interesting fact from another recently created article, then please feel free to nominate it.

HurricaneZetaC 00:02, 22 February 2026 (UTC)

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