| Display title | Prader–Willi syndrome |
| Default sort key | Prader-Willi syndrome |
| Page length (in bytes) | 39,209 |
| Namespace ID | 0 |
| Page ID | 54996 |
| Page content language | en - English |
| Page content model | wikitext |
| Indexing by robots | Allowed |
| Number of page watchers | 253 |
| Number of page watchers who visited in the last 30 days | 2 |
| Number of redirects to this page | 17 |
| Counted as a content page | Yes |
| Wikidata item ID | Q594013 |
| Local description | Rare genetic disorder involving an imprinted genomic region |
| Central description | Rare genetic disorder |
| Page image |  |
| Page views in the past 30 days | |
| Edit | Allow all users (no expiry set) |
| Move | Allow all users (no expiry set) |
| Page creator | PierreAbbat (talk | contribs) |
| Date of page creation | 05:51, 5 June 2002 |
| Latest editor | 94.199.27.162 (talk) |
| Date of latest edit | 17:44, 22 August 2024 |
| Total number of edits | 1,557 |
| Recent number of edits (within past 30 days) | 1 |
| Recent number of distinct authors | 1 |
| Hidden categories (16) | This page is a member of 16 hidden categories (help):
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| Transcluded templates (120) | Pages transcluded onto the current version of this page (help):
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| Wikidata entities used in this page | - Prader–Willi syndrome
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- Title
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- Description: en
- Miscellaneous (e.g. aliases, entity existence)
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| Background color inline style rule exists without a corresponding text color | 1 |
