| Display title | Phenylketonuria |
| Default sort key | Phenylketonuria |
| Page length (in bytes) | 58,183 |
| Namespace ID | 0 |
| Page ID | 23251 |
| Page content language | en - English |
| Page content model | wikitext |
| Indexing by robots | Allowed |
| Number of page watchers | 234 |
| Number of page watchers who visited in the last 30 days | 7 |
| Number of redirects to this page | 28 |
| Counted as a content page | Yes |
| Wikidata item ID | Q194041 |
| Local description | Amino acid metabolic disorder |
| Central description | amino acid metabolic disorder that is characterized by a mutation in the gene for the hepatic enzyme phenylalanine hydroxylase (PAH), rendering it nonfunctional |
| 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 | Malcolm Farmer (talk | contribs) |
| Date of page creation | 09:02, 30 April 2001 |
| Latest editor | Ozzie10aaaa (talk | contribs) |
| Date of latest edit | 14:29, 25 October 2024 |
| Total number of edits | 2,302 |
| Recent number of edits (within past 30 days) | 0 |
| Recent number of distinct authors | 0 |
| Hidden categories (11) | This page is a member of 11 hidden categories (help):
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| Transcluded templates (109) | Pages transcluded onto the current version of this page (help):
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| Wikidata entities used in this page | - phenylketonuria
- Sitelink
- Statement: P1395
- Statement: P1461
- Title
- Statement: P5806
- Description: en
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| Duplicate IDs | 1 |
| Background color inline style rule exists without a corresponding text color | 3 |
