| Display title | Hemoglobin H disease |
| Default sort key | Hemoglobin H disease |
| Page length (in bytes) | 8,721 |
| Namespace ID | 0 |
| Page ID | 51464455 |
| 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 | 2 |
| Counted as a content page | Yes |
| Wikidata item ID | Q3144945 |
| Local description | Medical condition |
| Central description | alpha thalassemia that has material basis in contiguous gene deletion of the hemoglobin alpha-1 (HBA1) and alpha-2 (HBA2) genes on one chromosome 16, and a defect, deletional or nondeletional, in either HBA1 or HBA2 on the other |
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| Edit | Allow all users (no expiry set) |
| Move | Allow all users (no expiry set) |
| Page creator | Keilana (talk | contribs) |
| Date of page creation | 15:03, 30 August 2016 |
| Latest editor | 185.169.7.173 (talk) |
| Date of latest edit | 14:34, 26 April 2024 |
| Total number of edits | 40 |
| 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 (54) | Pages transcluded onto the current version of this page (help):
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| Wikidata entities used in this page | - hemoglobin H disease
- Sitelink
- Title
- Statement: P1461
- Statement: P1395
- Statement: P486
- Statement: P5806
- Description: en
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| Background color inline style rule exists without a corresponding text color | 1 |
