الگو:DiseaseDisorder infobox
Name = Down syndrome | ICD10 = Q90 | ICD9 = 758.0 | ICDO = | Image = Drill.jpg | Caption = Child with Down syndrome using an electric screwdriver. | OMIM = 190685 | OMIM_mult = | MedlinePlus = 000997 | eMedicineSubj = ped | eMedicineTopic = 615 | DiseasesDB = 3898 | Cause = Trisomy 21 |
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Use this template freely for any medical condition that has an طبقهبندی بینالمللی آماری بیماریها code, میراث مندلی در انسان entry, سرعنوانهای موضوعی پزشکی, مرور ژن ID, or other source that you think readers will benefit from seeing. Its use is not limited strictly to diseases.
Usage summary
ویرایشThe template does not at the current time include summary information about the condition itself. Instead, it contains a consistent interface to other sources that provide information about the condition. Don't worry about trying to fill in all the fields -- even if you can only get one or two, that still can be useful.
While editing a condition, copy and paste the following text at the top of the page:
DiseaseDisorder infobox | |
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طبقهبندی و منابع بیرونی | |
آیسیدی-۱۰ | GroupMajor.minor |
آیسیدی-۹-سیام | xxx |
{{Infobox disease | Name = {{subst:PAGENAME}} | Image = | Alt = | Caption = | DiseasesDB = | ICD10 = {{ICD10|Group|Major|minor|LinkGroup|LinkMajor}} | ICD9 = {{ICD9|xxx}} | ICDO = | OMIM = | MedlinePlus = | eMedicineSubj = | eMedicineTopic = | MeSH = | GeneReviewsNBK = | GeneReviewsName = }}
The best place to start is often the دادگان بیماریها searching at DiseasesDB. Click on that link, and type in the name of the condition (for example, "Earache".) Click on the result you were looking for. At this point, you will see on your URL line something like "http://www.diseasesdatabase.com/ddb18027.htm". You can copy the number (in this case, "18027" onto the "DiseasesDB" line in the template, so it looks like this:
| DiseasesDB = 18027
You will see a label that reads "Code translations and terms via UMLS.". Click on this link. The goal is to find the ICD9 and ICD10 codes. In this case, you can see "388.7" next to "ICD-9-CM, 2006" and "H92.0" next to "German translation of ICD10, 1995". Fill in these two fields:
| ICD10 = H92.0 | ICD9 = {{ICD9|388.7}}
You may find multiple codes listed. In this case, just fill them out as follows:
| ICD10 = A11, B22 | ICD9 = {{ICD9|123}}, {{ICD9|456}}
In some cases, only one of the codes would apply to the current condition, but you may not always be able to determine which is which. Be bold, and do your best.
You will notice that there are direct links provided for the ICD9 codes, but not for ICD10. Don't worry about providing direct links for ICD10 codes unless you are feeling very ambitious. Some of the technical issues involved are discussed at Template:ICD10. However, the easiest way to put in a direct link is to go to List of ICD-10 codes and copy an example from there.
For the brave, the ICD10 template takes 5 parameters: {{ICD10|Group|Major|minor|LinkGroup|LinkMajor}}
- Group - The upper-case Group letter to be displayed in Wikipedia
- Major - Major group number (2 digits)
- minor - Minor group number (optional)
- LinkGroup - lower-case repeat of the Group letter to be presented to the WHO's website
- LinkMajor - The major coding at the top of webpage in which the target code exists (may or may not be the same as the Major code !)
In most cases you can skip over the "ICD-O" field, because that only applies to conditions that cause tumors. DiseasesDB does not provide these codes, but there are some resources listed for finding them at طبقهبندی بینالمللی بیماریهای انکولوژی.
The final three fields are for میراث مندلی در انسان, مدلاین پلاس, and ئیمدیسین. It's perfectly fine to leave these blank, but if you want to fill them out, you can sometimes find the pages by clicking on "specific web sites" in DiseaseDatabase. Alternatively use the following links to directly search OMIM, MedlinePlus and eMedicine.
Don't enter the full URL as this template's parameters, just the number at the end.
For eMedicine, two methods are acceptable as the website has restructured itself, but internally will redirect as required.
The old style, and hence the current parameter name usage, has two fields - put the number at the end into "eMedicineTopic", and put the alphabetic code (such as "neuro" or "orthoped") that precedes it into "eMedicineSubj".
The current eMedicine site now uses a fixed 'article' space with an 'article number', and hence please use:
| eMedicineSubj = article (this being a fixed literal text) | eMedicineTopic = 806890 (this being the variable article number)
It is a little trickier to fill out the infobox if you can't find it listed in DiseaseDatabase. However, you can look up the codes individually if you would like. A good source for ICD9 codes is here, and a good source for ICD10 codes is here. Many more sources for ICD codes are listed at طبقهبندی بینالمللی آماری بیماریها. You can look up OMIM codes here.
Images
ویرایشYou can use the "Image", "Alt" and "Caption" to provide an illustration. These fields are optional, but it is helpful to provide an image if you can find one. The Alt field specifies alt text, for readers who cannot see the image; see WP:ALT. Of course most images on the internet are copyrighted, but you may be able to find an image already in Wikipedia on a related page. There are over a thousand free images of anatomical structures available at فهرست تصویرها و موضوعات آناتومی گری. You could use one of these directly, or if you were feeling ambitious you could load one into a paint program on your computer, and annotate it with a couple of arrows to illustrate the point. Or just open مایکروسافت پاورپوینت and spend a few minutes drawing a few circles. It doesn't have to be very fancy to be an improvement on having no image at all. But if you do create a new image, remember to upload it at Wikimedia, not at Wikipedia, so that it easier to share images across languages.
There is also an optional "Width" parameter you can add for the image. If your picture is far too big, then add a new line and specify a custom width like this:
| Image = mypicture.png | Alt = A man's neck and shoulders, covered with giant green spots. | Caption = The picture above illustrates a severe case of this condition. | Width = 325
When no Width parameter is specified, it defaults to a width of 190.
Multiple-value fields
ویرایشSometimes you will find a condition with more than one entry for OMIM, eMedicine, MedlinePlus, or DiseaseDatabase. There are optional "_mult" fields that allow additional parameters to be passed in, with "helper templates" {{DiseasesDB2}}, {{OMIM2}}, {{MedlinePlus2}}, and {{eMedicine2}} that can be used to form the links..
Note that the "_mult" field should be used in addition to the normal field. The following illustrates the field names and the helper templates.
| DiseasesDB = number1 | DiseasesDB_mult = {{DiseasesDB2|number2}} ... | OMIM = number1 | OMIM_mult = {{OMIM2|number2}} ... | MedlinePlus = number1 | MedlinePlus_mult = {{MedlinePlus2|number2}} ... | eMedicineSubj = subj1 | eMedicineTopic = topic1 | eMedicine_mult = {{eMedicine2|subj2|topic2}} ...
Multiple MeSH values and multiple GeneReviews are handled differently. If there are multiple MeSH fields, just label each consecutive one MeSH2, MeSH3, etc. Likewise, use GeneReviewsNBK2, GeneReviewsName2, GeneReviewsNBK3, GeneReviewsName3, etc., for additional GeneReviews links.
An example of how this is used at is provided below (the values are mostly contrived).
DiseaseDisorder infobox | |
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طبقهبندی و منابع بیرونی | |
آیسیدی-۱۰ | G71.2 |
آیسیدی-۹-سیام | 359.0 |
اُمیم | 161800 256030 605355 |
دادگان بیماریها | 31991 33448 33447 |
ئیمدیسین | neuro/۷۶ neuro/230 |
سمپ | D001321، D015518، D015518 |
مرور ژن |
{{Infobox disease | Name = {{subst:PAGENAME}} | Image = | Alt = | Caption = | DiseasesDB = 31991 | DiseasesDB_mult = {{DiseasesDB2|33448}} {{DiseasesDB2|33447}} | ICD10 = {{ICD10|G|71|2|g|70}} | ICD9 = {{ICD9|359.0}} | ICDO = | OMIM = 161800 | OMIM_mult = {{OMIM2|256030}} {{OMIM2|605355}} | MedlinePlus = | MedlinePlus_mult= | eMedicineSubj = neuro | eMedicineTopic = 76 | eMedicine_mult = {{eMedicine2|neuro|230}} | MeSH = D001321 | MeSH2 = D015518 | MeSH3 = D015518 | GeneReviewsNBK = NBK5201 | GeneReviewsName = FBLN5-Related Cutis Laxa | GeneReviewsNBK2 = NBK5200 | GeneReviewsName2 = ATP6V0A2-Related CL }}
If there are too many eMedicine articles to list with eMedicine_mult, then one may directly show eMedicine's search list of topics.
Set eMedicineSubj = search and eMedicineTopic to the term to be searched for.
Note that any spaces in the search term must be replaced with the asci code of %20. Hence:
DiseaseDisorder infobox | |
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طبقهبندی و منابع بیرونی | |
ئیمدیسین | فهرست موضوعی |
{{Infobox disease | eMedicineSubj = search | eMedicineTopic = shaken%20baby%20syndrome }}
Don't worry about getting all the fields -- just do your best, and if you have any questions or suggestions, feel free to ask at Template talk:Infobox disease.
MeSH
ویرایشThe سرعنوانهای موضوعی پزشکی (MeSH), formerly known as the Supplement to Index medicus, is a controlled vocabulary managed by the کتابخانه ملی پزشکی ایالات متحده آمریکا. To find the MeSH code for a disease, go to the MeSH search page and enter the term into the search box. The needed MeSH number is the Unique ID in the MeSH Descriptor Page.
If more than one MeSH topic applies to a given condition (as, for example, in Hereditary leiomyomatosis and renal cell cancer) you can add additional values in a list, as described above.
GeneReviews
ویرایشمرور ژن is an online collection of peer-reviewed articles that describe specific gene-releated diseases. To use it, go to its home page on NCBI and in the search box, enter the disease name to see if there is a relevant gene review for this disease. For example, searching for "autism", the first hit is "Autism Spectrum Disorders", at the URL http://www.ncbi.nlm.nih.gov/books/NBK1442/
. Note the "NBK" number, which is the ID number of this review. It can be coded as follows:
DiseaseDisorder infobox | |
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طبقهبندی و منابع بیرونی | |
مرور ژن |
{{Infobox disease | GeneReviewsNBK = NBK1442 | GeneReviewsName = Autism Spectrum Disorders }}
If the condition has more than one relevant GeneReview, then you can enter these as shown in the example above, under "Multiple value fields".