| Display title | IPEX syndrome |
| Default sort key | IPEX syndrome |
| Page length (in bytes) | 20,544 |
| Namespace ID | 0 |
| Page ID | 4104309 |
| Page content language | en - English |
| Page content model | wikitext |
| Indexing by robots | Allowed |
| Number of page watchers | Fewer than 30 watchers |
| Number of redirects to this page | 9 |
| Counted as a content page | Yes |
| Wikidata item ID | Q3508566 |
| Local description | Medical condition |
| Central description | hypersensitivity reaction type II disease characterized by onset in infancy of refractory diarrhea, endocrinopathies, type 1 diabetes mellitus, and dermatitis that has material basis in mutation in the FOXP3 gene on chromosome Xp11 |
| 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 | Plutor (talk | contribs) |
| Date of page creation | 12:35, 17 February 2006 |
| Latest editor | 167.201.243.132 (talk) |
| Date of latest edit | 15:32, 23 August 2023 |
| Total number of edits | 315 |
| Recent number of edits (within past 30 days) | 0 |
| Recent number of distinct authors | 0 |
| Hidden categories (4) | This page is a member of 4 hidden categories (help):
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| Transcluded templates (88) | Pages transcluded onto the current version of this page (help):
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| Wikidata entities used in this page | |
| Background color inline style rule exists without a corresponding text color | 1 |
