Rollcloud

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Happy editing! HopsonRoad (talk) 21:08, 11 February 2021 (UTC)

Superfluous photos

Hi:

It seems you like to upload cloud photos in Commons and place them into articles. It is good to upload meaningful images but their use has to be justified. One only place a photo in an article to clarifying or illustrate a point. Wikipedia is not your photo album, please don't only add photos in articles just because you want to show your work.

Pierre cb (talk) 16:12, 31 March 2021 (UTC)

March 2021

Please refrain from uploading disruptive images with no encyclopedic value, such as Flood. It is considered vandalism. Thank you.  Velella  ^{Velella Talk}   18:25, 31 March 2021 (UTC)

April 2021

Please do not add inappropriate images to Wikipedia, as you did to Silliness; it is considered vandalism. If you would like to experiment, please use your sandbox. Please only add images if they add significant encyclopaedic value to an article and illustrate relevant text  Velella  ^{Velella Talk}   13:49, 5 April 2021 (UTC)

I concur with Pierre cb and Velella. Adding superfluous illustrations is detrimental to the quality of articles, and takes a lot of works by other users to be fixed. If you are not sure that a picture improves an article, then do not add it. Note that three users have come on your page independently for the exact same reason in the past month. Best, Malparti (talk) 15:41, 15 April 2021 (UTC)

Thanks, I appreciate your recommendations, I will not put files with no encyclopaedic value on Wikipedia articles, nor will I post useless pictures on Wikimedia Commons. Couch-scratching-cats (talk) 22:00, 15 April 2021 (UTC)

And yet you have just added two very low value images to Flood. Please stop now or risk some more formal sanctions.  Velella  ^{Velella Talk}   16:41, 1 May 2021 (UTC)

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Thanks for informing me, I have removed the link. Couch-scratching-cats (talk) 05:59, 11 April 2021 (UTC)

Hi Couch-scratching-cats, as you seem to be new to Wikipedia I just wanted to let you know that users whose name ends with "bot" are bots, i.e. computer programs, not real persons. So there is no need to reply to them. Best, Malparti (talk) 15:20, 15 April 2021 (UTC)

Altocumulus lacunosus cloud moved to draftspace

An article you recently created, Altocumulus lacunosus cloud, is not suitable as written to remain published. It needs citations from reliable, independent sources. (?) Information that can't be referenced should be removed (verifiability is of central importance on Wikipedia). I've moved your draft to draftspace (with a prefix of "Draft:" before the article title) where you can incubate the article with minimal disruption. When you feel the article meets Wikipedia's general notability guideline and thus is ready for mainspace, please click on the "Submit your draft for review!" button at the top of the page. JW 1961 ^Talk 21:27, 12 November 2021 (UTC)

Yes, while editing I had to go from the place I was in to another place and I didn't have time to finish it, I'm going to start gathering my sources and then I will move the page from draft to article. Kind regards, Couch-scratching-cats (talk) 01:36, 13 November 2021 (UTC)

Proposed deletion of Cumulonimbus cauda

The article Cumulonimbus cauda has been proposed for deletion because of the following concern:

I am unable to find reliable (scientific, meteorological) sources that mention this type of cloud.

While all constructive contributions to Wikipedia are appreciated, pages may be deleted for any of several reasons.

You may prevent the proposed deletion by removing the {{proposed deletion/dated}} notice, but please explain why in your edit summary or on the article's talk page.

Please consider improving the page to address the issues raised. Removing {{proposed deletion/dated}} will stop the proposed deletion process, but other deletion processes exist. In particular, the speedy deletion process can result in deletion without discussion, and articles for deletion allows discussion to reach consensus for deletion. ... discospinster _talk 21:12, 16 November 2021 (UTC)

Proposed deletion of Opacus (cloud variety)

The article Opacus (cloud variety) has been proposed for deletion because of the following concern:

No citations

While all constructive contributions to Wikipedia are appreciated, pages may be deleted for any of several reasons.

You may prevent the proposed deletion by removing the {{proposed deletion/dated}} notice, but please explain why in your edit summary or on the article's talk page.

Please consider improving the page to address the issues raised. Removing {{proposed deletion/dated}} will stop the proposed deletion process, but other deletion processes exist. In particular, the speedy deletion process can result in deletion without discussion, and articles for deletion allows discussion to reach consensus for deletion. Leomk (Don't shout here, Shout here!) 02:47, 19 November 2021 (UTC)

Ways to improve Opacus (cloud variety)

Hello, Rollcloud,

Thank you for creating Opacus (cloud variety).

I have tagged the page as having some issues to fix, as a part of our page curation process and note that:

To satisfy WP:GNG, you need to demonstrate that there is significant coverage in multiple independent secondary sources not just a single source.

The tags can be removed by you or another editor once the issues they mention are addressed. If you have questions, leave a comment here and begin it with {{Re|Dan arndt}}. Remember to sign your reply with ~~~~. For broader editing help, please visit the Teahouse.

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Dan arndt (talk) 03:03, 19 November 2021 (UTC)

Ways to improve Perlucidus (cloud variety)

Hello, Rollcloud,

Thank you for creating Perlucidus (cloud variety).

I have tagged the page as having some issues to fix, as a part of our page curation process and note that:

To satisfy WP:GNG, you need to demonstrate that there is significant coverage in multiple independent secondary sources.

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Dan arndt (talk) 03:05, 19 November 2021 (UTC)

Ways to improve Stratocumulus lenticularis

Hello, Rollcloud,

Thank you for creating Stratocumulus lenticularis.

I have tagged the page as having some issues to fix, as a part of our page curation process and note that:

To satisfy WP:GNG, you need to demonstrate that there is significant coverage in multiple independent secondary sources not just a single source.

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Dan arndt (talk) 03:07, 19 November 2021 (UTC)

Ways to improve Translucidus (cloud variety)

Hello, Rollcloud,

Thank you for creating Translucidus (cloud variety).

I have tagged the page as having some issues to fix, as a part of our page curation process and note that:

To satisfy WP:GNG, you need to demonstrate that there is significant coverage in multiple independent secondary sources not just a single source.

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Dan arndt (talk) 03:09, 19 November 2021 (UTC)

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December 2021

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An automated process has detected that when you recently edited Gringo, you added a link pointing to the disambiguation page European.

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Cirrus cloud

I have nominated Cirrus cloud for a featured article review here. Please join the discussion on whether this article meets featured article criteria. Articles are typically reviewed for two weeks. If substantial concerns are not addressed during the review period, the article will be moved to the Featured Article Removal Candidates list for a further period, where editors may declare "Keep" or "Delist" the article's featured status. The instructions for the review process are here. Chidgk1 (talk) 09:11, 14 February 2022 (UTC)

A cookie for you!

Thank you for creating Brachymetacarpia! Tow (talk) 16:29, 27 March 2022 (UTC)

Tips for your new articles

I noticed you are making a lot of new articles for rare genetic disorders. Just want to pass on some tips (I've tried to do the following to some of your articles, but it would be helpful if you could update your new articles with these suggestions and keep them in mind for your future articles):

• Bold the subject's name in the lead. I've noticed you miss this on occasion, but it is part of Wikipedia's manual of style.

• Add a References section. Add a section at the end of the article with == References == and in the next line use something like {{reflist}}.

• Try to avoid bare URLs for your references. This can cause WP: Link rot. That page gives some suggestions of how to avoid it.

• Add WP:Categories to the end of the article

• Add links to the article in other Wikipedia pages. Otherwise, it is an WP:Orphan

• Add the article to WikiProjects. This generates more editor interest in the articles. I would suggest WP:Medicine with their medical genetics taskforce. You can do that by adding {{WikiProject Medicine|genetics=yes}} in the article's talk page.

Hope that helps. Singularity42 (talk) 19:16, 10 May 2022 (UTC)

Thank you, I'll have these in my mind when I make new articles:) kind regards, Rollcloud (talk) 19:42, 10 May 2022 (UTC)

Aniridia - ptosis - intellectual disability - familial obesity moved to draftspace

An article you recently created, Aniridia - ptosis - intellectual disability - familial obesity, is not suitable as written to remain published. It needs more citations from reliable, independent sources. (?) Information that can't be referenced should be removed (verifiability is of central importance on Wikipedia). I've moved your draft to draftspace (with a prefix of "Draft:" before the article title) where you can incubate the article with minimal disruption. When you feel the article meets Wikipedia's general notability guideline and thus is ready for mainspace, please click on the "Submit your draft for review!" button at the top of the page. PRAXIDICAE💕 20:25, 11 May 2022 (UTC)

Deafness-epiphyseal dysplasia-short stature syndrome moved to draftspace - no references, no categories, no links to other pages.

An article you recently created, Deafness-epiphyseal dysplasia-short stature syndrome, is not suitable as written to remain published. It needs more citations from reliable, independent sources. (?) Information that can't be referenced should be removed (verifiability is of central importance on Wikipedia). I've moved your draft to draftspace (with a prefix of "Draft:" before the article title) where you can incubate the article with minimal disruption. When you feel the article meets Wikipedia's general notability guideline and thus is ready for mainspace, please click on the "Submit your draft for review!" button at the top of the page. This article needs to follow the Manual of Style Whiteguru (talk) 02:22, 18 May 2022 (UTC)

Hi, can you point out what parts you thought were unreferenced/what references you think are unreliable? All of the information I wrote had citations coming from PubMed and such. I'm asking just so I can know what to work on in the article of course. kind regards, Rollcloud (talk) 02:26, 18 May 2022 (UTC)

Ways to improve Tel Hashomer camptodactyly syndrome

Hello, Rollcloud,

Thank you for creating Tel Hashomer camptodactyly syndrome.

I have tagged the page as having some issues to fix, as a part of our page curation process and note that:

This article needs to go beyond Cases and provide some context for this genetic disorder. There is no context for a reader.

The tags can be removed by you or another editor once the issues they mention are addressed. If you have questions, leave a comment here and begin it with {{Re|Whiteguru}}. Remember to sign your reply with ~~~~. For broader editing help, please visit the Teahouse.

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Whiteguru (talk) 03:27, 18 May 2022 (UTC)

AfC notification: Draft:Deafness-epiphyseal dysplasia-short stature syndrome has a new comment

I've left a comment on your Articles for Creation submission, which can be viewed at Draft:Deafness-epiphyseal dysplasia-short stature syndrome. Thanks! Robert McClenon (talk) 01:51, 19 May 2022 (UTC)

Nomination of Arthrogryposis multiplex with deafness, inguinal hernias, and early death for deletion

A discussion is taking place as to whether the article Arthrogryposis multiplex with deafness, inguinal hernias, and early death is suitable for inclusion in Wikipedia according to Wikipedia's policies and guidelines or whether it should be deleted.

The article will be discussed at Wikipedia:Articles for deletion/Arthrogryposis multiplex with deafness, inguinal hernias, and early death until a consensus is reached, and anyone, including you, is welcome to contribute to the discussion. The nomination will explain the policies and guidelines which are of concern. The discussion focuses on high-quality evidence and our policies and guidelines.

Users may edit the article during the discussion, including to improve the article to address concerns raised in the discussion. However, do not remove the article-for-deletion notice from the top of the article.

— Ⓜ️hawk10 (talk) 05:59, 23 May 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Familial thoracic aortic aneurysm and aortic dissection.

User:SunDawn, while examining this page as a part of our page curation process, had the following comments:

Thanks for creating the article!

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✠ SunDawn ✠ (contact) 06:30, 25 May 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Nestor-Guillermo progeria syndrome.

User:SunDawn, while examining this page as a part of our page curation process, had the following comments:

Thanks for the article!

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✠ SunDawn ✠ (contact) 15:12, 29 May 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating 7p22.1 microduplication syndrome.

User:SunDawn, while examining this page as a part of our page curation process, had the following comments:

Thanks for the article!

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✠ SunDawn ✠ (contact) 15:46, 29 May 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Absent tibia-polydactyly-arachnoid cyst syndrome.

User:North8000, while examining this page as a part of our page curation process, had the following comments:

Nice work

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North8000 (talk) 02:13, 3 June 2022 (UTC)

A barnstar for you!

	The Writer's Barnstar
	For many stub articles and non-stub articles on many rare genetic conditions. Robert McClenon (talk) 03:33, 3 June 2022 (UTC)

Reference error messages

Hello, I have fixed a number of ref-error msgs over the last few weeks in pages you have edited or created; these mainly have had to do with the large gaps in the titles of the OMIM references which produce a 'line feed' error message and adds the page to an ever-expanding category. These messages are usually displayed in red in the refs section next to the cite concerned. Please use preview to check the refs and fix. Thank you. Happy editing. Eagleash (talk) 09:31, 3 June 2022 (UTC)

Hello, I have noticed and I just learned how to fix the ref line feed error by removing the gaps, and I sometimes I forget to remove them. I will be mindful about this later. kind regards, Rollcloud (talk) 18:27, 3 June 2022 (UTC)

Thank you, I've just fixed several errors at Tucker syndrome. Please remember to check the refs list for errors. Cheers. Eagleash (talk) 01:59, 4 June 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Chudley-Mccullough syndrome.

User:SunDawn, while examining this page as a part of our page curation process, had the following comments:

Thanks for the article! It would be better if the orphan status is removed though.

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✠ SunDawn ✠ (contact) 02:09, 7 June 2022 (UTC)

PRICKLE1-related progressive myoclonus epilepsy with ataxia

Please fix the error messages. Eagleash (talk) 03:54, 7 June 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Polyonychia.

User:SunDawn, while examining this page as a part of our page curation process, had the following comments:

Thanks for creating the article!

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✠ SunDawn ✠ (contact) 01:27, 8 June 2022 (UTC)

Proud syndrome

Four more ref error messages (out of a total of five citations). Do you actually check your work before saving it? WP:CIR. The errors brought to your attention in several examples on this page are not the only instances and you need to heed the communications. Eagleash (talk) 20:40, 13 June 2022 (UTC)

I'm a forgetful person but yes I will fix ref error messages next time, I started working on it by fixing the spaces between "OMIM Entry" in Omim references, then by fixing them on PubMed date errors where only the month and year is added instead of the day itself. I will remind myself of this constantly next time. If i don't fix them before I first publish the article I will fix them afterwards. kind regards, Rollcloud (talk) 21:32, 13 June 2022 (UTC)

Articles on extremely rare genetic disorders

There's a discussion regarding articles you created at WT:MED#Articles on extremely rare genetic disorders. It would be useful if you could explain why you are creating these articles. -- Colin°^Talk 10:47, 15 June 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Palmoplantar keratoderma with deafness.

User:North8000, while examining this page as a part of our page curation process, had the following comments:

Nice work

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North8000 (talk) 17:33, 26 June 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons.

User:North8000, while examining this page as a part of our page curation process, had the following comments:

Thanks for your work

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North8000 (talk) 17:33, 26 June 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating GOSR2-related progressive myoclonus ataxia.

User:North8000, while examining this page as a part of our page curation process, had the following comments:

Good start. I marked it as reviewed. Happy editing!

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North8000 (talk) 17:34, 26 June 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Pierre Robin sequence-faciodigital anomaly syndrome.

User:North8000, while examining this page as a part of our page curation process, had the following comments:

Thanks for your work

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North8000 (talk) 17:35, 26 June 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Marsili syndrome.

User:North8000, while examining this page as a part of our page curation process, had the following comments:

Thanks for your work

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North8000 (talk) 17:35, 26 June 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Triphalangeal thumbs-brachyectrodactyly syndrome.

User:North8000, while examining this page as a part of our page curation process, had the following comments:

Good start. I marked it as reviewed. Happy editing!

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North8000 (talk) 17:36, 26 June 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Iris hypoplasia with glaucoma.

User:North8000, while examining this page as a part of our page curation process, had the following comments:

Good start. I marked it as reviewed. Happy editing!

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North8000 (talk) 17:37, 26 June 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Trigonocephaly-bifid nose-acral anomalies syndrome.

User:North8000, while examining this page as a part of our page curation process, had the following comments:

Thanks for your work

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North8000 (talk) 17:38, 26 June 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Megalocornea-intellectual disability syndrome.

User:North8000, while examining this page as a part of our page curation process, had the following comments:

Thanks for your work

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North8000 (talk) 17:40, 26 June 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Pai syndrome.

User:North8000, while examining this page as a part of our page curation process, had the following comments:

thanks for your work

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North8000 (talk) 17:41, 26 June 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Mirror polydactyly-vertebral segmentation-limb defects syndrome.

User:North8000, while examining this page as a part of our page curation process, had the following comments:

Good start. I marked it as reviewed. Happy editing!

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North8000 (talk) 17:42, 26 June 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Scalp defects-postaxial polydactyly syndrome.

User:North8000, while examining this page as a part of our page curation process, had the following comments:

Good start. I marked it as reviewed. Happy editing!

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North8000 (talk) 17:42, 26 June 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Mirror polydactyly-vertebral segmentation-limb defects syndrome.

User:North8000, while examining this page as a part of our page curation process, had the following comments:

Good start. I marked it as reviewed. Happy editing!

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North8000 (talk) 17:43, 26 June 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating X-linked sideroblastic anemia and spinocerebellar ataxia.

User:North8000, while examining this page as a part of our page curation process, had the following comments:

Good start. I marked it as reviewed. Happy editing!

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North8000 (talk) 17:43, 26 June 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Early-onset parkinsonism-intellectual disability syndrome.

User:North8000, while examining this page as a part of our page curation process, had the following comments:

Nice work

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North8000 (talk) 17:44, 26 June 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Metacarpal synostosis.

User:North8000, while examining this page as a part of our page curation process, had the following comments:

Nice work

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North8000 (talk) 17:44, 26 June 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Growth delay-hydrocephaly-lung hypoplasia syndrome.

User:North8000, while examining this page as a part of our page curation process, had the following comments:

Nice work

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North8000 (talk) 17:45, 26 June 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Growth delay-hydrocephaly-lung hypoplasia syndrome.

User:North8000, while examining this page as a part of our page curation process, had the following comments:

Nice work

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North8000 (talk) 17:47, 26 June 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Autism with port-wine stain syndrome.

User:North8000, while examining this page as a part of our page curation process, had the following comments:

Good start. I marked it as reviewed. Happy editing!

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North8000 (talk) 17:48, 26 June 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating GATAD2B-associated neurodevelopmental disorder.

User:North8000, while examining this page as a part of our page curation process, had the following comments:

Thanks again for your work

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North8000 (talk) 17:48, 26 June 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Sergio Arias Cazorla.

User:North8000, while examining this page as a part of our page curation process, had the following comments:

Nice work

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North8000 (talk) 17:51, 26 June 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Fine-Lubinsky syndrome.

User:North8000, while examining this page as a part of our page curation process, had the following comments:

Good start. I marked it as reviewed. Happy editing!

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North8000 (talk) 17:53, 26 June 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Hamanishi Ueba Tsuji syndrome.

User:North8000, while examining this page as a part of our page curation process, had the following comments:

Good start. I marked it as reviewed. Happy editing!

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North8000 (talk) 17:55, 26 June 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Spastic paraplegia 6.

User:Kudpung, while examining this page as a part of our page curation process, had the following comments:

Please clean up any naked URLs in the sources. Try to find additional appropriate categories (used perhaps in parent or linked articles?)

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Kudpung กุดผึ้ง (talk) 21:52, 1 July 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Short-limb skeletal dysplasia with severe combined immunodeficiency.

User:Kudpung, while examining this page as a part of our page curation process, had the following comments:

Cats added and review passed. Please add appropriate Wikiproject banner to talk page.

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Kudpung กุดผึ้ง (talk) 15:52, 5 July 2022 (UTC)

Czech dysplasia, metatarsal type moved to draftspace

An article you recently created, Czech dysplasia, metatarsal type, is not suitable as written to remain published. It needs more citations from reliable, independent sources. (?) Information that can't be referenced should be removed (verifiability is of central importance on Wikipedia). I've moved your draft to draftspace (with a prefix of "Draft:" before the article title) where you can incubate the article with minimal disruption. When you feel the article meets Wikipedia's general notability guideline and thus is ready for mainspace, please click on the "Submit your draft for review!" button at the top of the page. Iseult ^Δx parlez moi 15:09, 7 July 2022 (UTC)

I'm working on that atm.

Usually I try to complete the article before I create it but I spent a lot of time writing this one and all of it went to waste when the page refreshed while I was looking for one of my sources. kind regards, Rollcloud (talk) 15:42, 7 July 2022 (UTC)

Your submission at Articles for creation: Czech dysplasia, metatarsal type has been accepted

Czech dysplasia, metatarsal type, which you submitted to Articles for creation, has been created.

Congratulations, and thank you for helping expand the scope of Wikipedia! We hope you will continue making quality contributions.

The article has been assessed as Stub-Class, which is recorded on its talk page. It is commonplace for new articles to start out as stubs and then attain higher grades as they develop over time. You may like to take a look at the grading scheme to see how you can improve the article.

Since you have made at least 10 edits over more than four days, you can now create articles yourself without posting a request. However, you may continue submitting work to Articles for creation if you prefer.

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Thanks again, and happy editing!

 DIVINE  17:56, 7 July 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Osteoporosis-pseudoglioma syndrome.

User:SunDawn, while examining this page as a part of our page curation process, had the following comments:

Thanks for the article!

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✠ SunDawn ✠ (contact) 03:50, 12 July 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating Intellectual disability-spasticity-ectrodactyly syndrome.

User:Bruxton, while examining this page as a part of our page curation process, had the following comments:

I reviewed your article. Keep it going!

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Bruxton (talk) 04:29, 13 July 2022 (UTC)

Ways to improve Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome

Hello, Rollcloud,

Thank you for creating Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome.

I have tagged the page as having some issues to fix, as a part of our page curation process and note that:

A few too many sections. Can you reduce the amount please?

The tags can be removed by you or another editor once the issues they mention are addressed. If you have questions, leave a comment here and begin it with {{Re|CollectiveSolidarity}}. Remember to sign your reply with ~~~~. For broader editing help, please visit the Teahouse.

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CollectiveSolidarity (talk) 23:33, 13 July 2022 (UTC)

Disambiguation link notification for July 14

An automated process has detected that when you recently edited Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome, you added a link pointing to the disambiguation page Gene sequencing.

(Opt-out instructions.) --DPL bot (talk) 09:27, 14 July 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud

Thank you for creating X-linked Charcot-Marie-Tooth disease.

User:SunDawn, while examining this page as a part of our page curation process, had the following comments:

Thanks for the article!

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✠ SunDawn ✠ (contact) 03:52, 20 July 2022 (UTC)

Article creation

Hello, Rollcloud,

First, thank you for all of your contributions to Wikipedia. They are appreciated! However, it would help other editors if you would start articles in Draft space or User space like your Sandbox rather than putting them in main space and then moving them to Draft space and then moving them back to main space. All of these page moves puts your articles on a list of pages that have been moved and each time you move a page from main space to Draft space, it creates a redirect that then has to be tagged for deletion and deleted by an administrator. It would be much simpler if you worked in Draft or User space and only moved an article into main space when you thought it was "finished". It also complicates things because our New Page Patrollers are reviewing an unfinished Draft in main space and they could easily tag it for deletion. If you just put articles into main space when you are done with a draft, then the NPP will be reviewing a much more polished version of the article.

Thank you for considering changing up your procedure for creating articles! Liz ^{Read! Talk!} 03:36, 10 September 2022 (UTC)

Thanks for notifying me, really appreciate it, I will write my articles from one of those two spaces from now on. kind regards, Rollcloud (talk) 04:08, 10 September 2022 (UTC)

Disambiguation link notification for September 10

An automated process has detected that you recently added links to disambiguation pages.

Autosomal dominant cerebellar ataxia, deafness, and narcolepsy

added a link pointing to Swedish

Pulmonary atresia with ventricular septal defect

added a link pointing to Britain

(Opt-out instructions.) --DPL bot (talk) 09:13, 10 September 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud. Thank you for creating Sonoda syndrome. User:Bruxton, while examining this page as a part of our page curation process, had the following comments:

Thanks for the article!

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Bruxton (talk) 03:17, 11 September 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud. Thank you for creating Pulmonary atresia with ventricular septal defect. User:Bruxton, while examining this page as a part of our page curation process, had the following comments:

Thanks

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Bruxton (talk) 03:18, 11 September 2022 (UTC)

Disambiguation link notification for September 17

An automated process has detected that when you recently edited Autosomal dominant cerebellar ataxia, deafness, and narcolepsy, you added a link pointing to the disambiguation page Swedish.

(Opt-out instructions.) --DPL bot (talk) 09:05, 17 September 2022 (UTC)

Your submission at Articles for creation: Deafness-epiphyseal dysplasia-short stature syndrome (September 21)

Your recent article submission to Articles for Creation has been reviewed! Unfortunately, it has not been accepted at this time. The reason left by Primefac was:  The comment the reviewer left was: Please check the submission for any additional comments left by the reviewer. You are encouraged to edit the submission to address the issues raised and resubmit after they have been resolved.

• If you would like to continue working on the submission, go to Draft:Deafness-epiphyseal dysplasia-short stature syndrome and click on the "Edit" tab at the top of the window.
• If you do not edit your draft in the next 6 months, it will be considered abandoned and may be deleted.
• If you need any assistance, or have experienced any untoward behavior associated with this submission, you can ask for help at the Articles for creation help desk, on the reviewer's talk page or use Wikipedia's real-time chat help from experienced editors.

Primefac (talk) 10:02, 21 September 2022 (UTC)

Disambiguation link notification for September 26

An automated process has detected that when you recently edited Familial opposable triphalangeal thumbs duplication, you added a link pointing to the disambiguation page German.

(Opt-out instructions.) --DPL bot (talk) 09:05, 26 September 2022 (UTC)

Disambiguation link notification for October 3

An automated process has detected that when you recently edited Adolescent idiopathic scoliosis, you added links pointing to the disambiguation pages Chinese and Trunk.

(Opt-out instructions.) --DPL bot (talk) 06:04, 3 October 2022 (UTC)

Replaceable fair use File:Family pedigree and electron micrographic image of the skeletal muscles of a patient with Compton-North congenital myopathy.jpg

Thanks for uploading File:Family pedigree and electron micrographic image of the skeletal muscles of a patient with Compton-North congenital myopathy.jpg. I noticed that this file is being used under a claim of fair use. However, I think that the way it is being used fails the first non-free content criterion. This criterion states that files used under claims of fair use may have no free equivalent; in other words, if the file could be adequately covered by a freely-licensed file or by text alone, then it may not be used on Wikipedia. If you believe this file is not replaceable, please:

1. Go to the file description page and add the text {{Di-replaceable fair use disputed|<your reason>}} below the original replaceable fair use template, replacing <your reason> with a short explanation of why the file is not replaceable.
2. On the file discussion page, write a full explanation of why you believe the file is not replaceable.

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If you have uploaded other non-free media, consider checking that you have specified how these media fully satisfy our non-free content criteria. You can find a list of description pages you have edited by clicking on this link. Note that even if you follow steps 1 and 2 above, non-free media which could be replaced by freely licensed alternatives will be deleted 2 days after this notification, per the non-free content policy. If you have any questions, please ask them at the Media copyright questions page. Thank you. — Red-tailed hawk _(nest) 20:44, 16 October 2022 (UTC)

I have sent you a note about a page you started

Hello, Rollcloud. Thank you for your work on Faciocardiorenal syndrome. User:Usernamekiran, while examining this page as a part of our page curation process, had the following comments:

Kindly add categories to the article, and wikiproject banners to the talkpage of the article. For reference, taking a look at the similar articles is recommended. Thanks.

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—usernamekiran (talk) 09:58, 28 October 2022 (UTC)

Concern regarding Draft:Aniridia - ptosis - intellectual disability - familial obesity

Hello, Rollcloud. This is a bot-delivered message letting you know that Draft:Aniridia - ptosis - intellectual disability - familial obesity, 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) 02:27, 30 October 2022 (UTC)

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Concern regarding Draft:Deafness-epiphyseal dysplasia-short stature syndrome

Hello, Rollcloud. This is a bot-delivered message letting you know that Draft:Deafness-epiphyseal dysplasia-short stature 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.

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Thank you for your submission to Wikipedia. FireflyBot (talk) 11:00, 21 February 2023 (UTC)

Your draft article, Draft:Deafness-epiphyseal dysplasia-short stature syndrome

Hello, Rollcloud. It has been over six months since you last edited the Articles for Creation submission or draft page you started, "Deafness-epiphyseal dysplasia-short stature syndrome".

In accordance with our policy that Wikipedia is not for the indefinite hosting of material deemed unsuitable for the encyclopedia mainspace, the draft 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 and remove the {{db-afc}}, {{db-draft}}, or {{db-g13}} code.

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Thank you for your submission to Wikipedia! Hey man im josh (talk) 12:08, 21 March 2023 (UTC)

Your submission at Articles for creation: Epidemiology of myopia has been accepted

Epidemiology of myopia, which you submitted to Articles for creation, has been created.

Congratulations, and thank you for helping expand the scope of Wikipedia! We hope you will continue making quality contributions.

The article has been assessed as C-Class, which is recorded on its talk page. This is a great rating for a new article, and places it among the top 21% of accepted submissions — kudos to you! You may like to take a look at the grading scheme to see how you can improve the article.

Since you have made at least 10 edits over more than four days, you can now create articles yourself without posting a request. However, you may continue submitting work to Articles for creation if you prefer.

If you have any questions, you are welcome to ask at the help desk. Once you have made at least 10 edits and had an account for at least four days, you will have the option to create articles yourself without posting a request to Articles for creation.

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Thanks again, and happy editing!

Clearfrienda ^💬 19:04, 24 April 2023 (UTC)

Nomination of Epidemiology of myopia for deletion

A discussion is taking place as to whether the article Epidemiology of myopia is suitable for inclusion in Wikipedia according to Wikipedia's policies and guidelines or whether it should be deleted.

The article will be discussed at Wikipedia:Articles for deletion/Epidemiology of myopia until a consensus is reached, and anyone, including you, is welcome to contribute to the discussion. The nomination will explain the policies and guidelines which are of concern. The discussion focuses on high-quality evidence and our policies and guidelines.

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Natg 19 (talk) 00:35, 5 May 2023 (UTC)

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