| Display title | Johnson–McMillin syndrome |
| Default sort key | Johnson-McMillin syndrome |
| Page length (in bytes) | 2,463 |
| Namespace ID | 0 |
| Page ID | 25477282 |
| 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 | 4 |
| Counted as a content page | Yes |
| Wikidata item ID | Q16940647 |
| Local description | Medical condition |
| Central description | Johnson neuroectodermal syndrome is characterised by alopecia, anosmia or hyposmia, conductive deafness with malformed ears and microtia and/or atresia of the external auditory canal, and hypogonadotropic hypogonadism |
| 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 | Calmer Waters (talk | contribs) |
| Date of page creation | 11:11, 18 December 2009 |
| Latest editor | IntentionallyDense (talk | contribs) |
| Date of latest edit | 02:11, 7 May 2024 |
| Total number of edits | 34 |
| Recent number of edits (within past 30 days) | 0 |
| Recent number of distinct authors | 0 |
| Hidden categories (3) | This page is a member of 3 hidden categories (help):
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| Transcluded templates (61) | 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 |
