| Display title | Medicine:Carbamoyl phosphate synthetase I deficiency |
| Default sort key | Carbamoyl phosphate synthetase I deficiency |
| Page length (in bytes) | 6,474 |
| Namespace ID | 3048 |
| Namespace | Medicine |
| Page ID | 531445 |
| Page content language | en - English |
| Page content model | wikitext |
| Indexing by robots | Allowed |
| Number of redirects to this page | 0 |
| Counted as a content page | Yes |
| HandWiki item ID | None |
| Edit | Allow all users (infinite) |
| Move | Allow all users (infinite) |
| Page creator | imported>WikiG |
| Date of page creation | 00:12, 5 February 2024 |
| Latest editor | imported>WikiG |
| Date of latest edit | 00:12, 5 February 2024 |
| Total number of edits | 1 |
| Recent number of edits (within past 90 days) | 0 |
| Recent number of distinct authors | 0 |
Description | Content |
Article description: (description)
This attribute controls the content of the description and og:description elements. | Carbamoyl phosphate synthetase I deficiency (CPS I deficiency) is an autosomal recessive metabolic disorder that causes ammonia to accumulate in the blood due to a lack of the enzyme carbamoyl phosphate synthetase I. Ammonia, which is formed when proteins are broken down in the body, is toxic if the... |
