| Display title | Kallmann syndrome |
| Default sort key | Kallmann syndrome |
| Page length (in bytes) | 47,184 |
| Namespace ID | 0 |
| Page ID | 1110898 |
| Page content language | en - English |
| Page content model | wikitext |
| Indexing by robots | Allowed |
| Number of page watchers | 109 |
| Number of page watchers who visited in the last 30 days | 3 |
| Number of redirects to this page | 8 |
| Counted as a content page | Yes |
| Wikidata item ID | Q1165179 |
| Local description | Genetic disorder which delays or stops puberty |
| Central description | A form of hypogonadotropic hypogonadism which is also accompanied by a total lack or partial loss in the sense of smell. The condition affects people with XX or XY chromosomes and causes atypical puberty and infertility. |
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| Edit | Allow all users (no expiry set) |
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| Page creator | Charm (talk | contribs) |
| Date of page creation | 09:36, 28 October 2004 |
| Latest editor | Citation bot (talk | contribs) |
| Date of latest edit | 22:02, 6 January 2025 |
| Total number of edits | 931 |
| Recent number of edits (within past 30 days) | 1 |
| Recent number of distinct authors | 1 |
| Hidden categories (8) | This page is a member of 8 hidden categories (help):
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| Transcluded templates (99) | Pages transcluded onto the current version of this page (help):
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| Wikidata entities used in this page | - Kallmann syndrome
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- Description: en
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| Duplicate IDs | 2 |
| Background color inline style rule exists without a corresponding text color | 1 |
