| Display title | Cystathioninuria |
| Default sort key | Cystathioninuria |
| Page length (in bytes) | 7,290 |
| Namespace ID | 0 |
| Page ID | 11469860 |
| 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 | Q5201186 |
| Local description | Medical condition |
| Central description | amino acid metabolic disorder characterized by elevated plasma and urinary cystathionine levels that has material basis in homozygous or compound heterozygous mutation in the CTH gene on chromosome 1p31 |
| 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 | Arcadian (talk | contribs) |
| Date of page creation | 17:42, 28 May 2007 |
| Latest editor | Ozzie10aaaa (talk | contribs) |
| Date of latest edit | 13:38, 15 October 2024 |
| Total number of edits | 56 |
| Recent number of edits (within past 30 days) | 2 |
| Recent number of distinct authors | 1 |
| Hidden categories (2) | This page is a member of 2 hidden categories (help):
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| Transcluded templates (59) | Pages transcluded onto the current version of this page (help):
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| Wikidata entities used in this page | - cystathioninuria
- Title
- Sitelink
- Statement: P1395
- Statement: P1461
- Statement: P486
- Statement: P5806
- Description: en
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| Background color inline style rule exists without a corresponding text color | 1 |
