| Display title | Haemophilia B |
| Default sort key | Haemophilia B |
| Page length (in bytes) | 17,897 |
| Namespace ID | 0 |
| Page ID | 199559 |
| Page content language | en - English |
| Page content model | wikitext |
| Indexing by robots | Allowed |
| Number of page watchers | 48 |
| Number of page watchers who visited in the last 30 days | 2 |
| Number of redirects to this page | 8 |
| Counted as a content page | Yes |
| Wikidata item ID | Q2562598 |
| Local description | Genetic X-linked recessive bleeding disorder |
| Central description | An inherited blood coagulation disease that has material basis in Factor IX deficiency, which makes coagulation much more prolonged. The disease is inherited as an X-linked recessive trait. |
| 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 | RTC (talk | contribs) |
| Date of page creation | 18:46, 21 March 2003 |
| Latest editor | Spoonyhistorian (talk | contribs) |
| Date of latest edit | 19:11, 17 December 2023 |
| Total number of edits | 350 |
| Recent number of edits (within past 30 days) | 0 |
| Recent number of distinct authors | 0 |
| Hidden categories (6) | This page is a member of 6 hidden categories (help):
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| Transcluded templates (103) | Pages transcluded onto the current version of this page (help):
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| Wikidata entities used in this page | - hemophilia B
- Sitelink
- Statement: P1395
- Statement: P1461
- Title
- Statement: P5806
- Description: en
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