| Display title | Medicine:Prolidase deficiency |
| Default sort key | Prolidase deficiency |
| Page length (in bytes) | 10,933 |
| Namespace ID | 3048 |
| Namespace | Medicine |
| Page ID | 532010 |
| 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 |
| Page image |  |
| HandWiki item ID | None |
| Edit | Allow all users (infinite) |
| Move | Allow all users (infinite) |
| Page creator | imported>Scavis2 |
| Date of page creation | 10:38, 14 February 2024 |
| Latest editor | imported>Scavis2 |
| Date of latest edit | 10:38, 14 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. | Prolidase deficiency (PD) is an extremely uncommon autosomal recessive disorder associated with collagen metabolism that affects connective tissues and thus a diverse array of organ systems more broadly, though it is extremely inconsistent in its expression.
Collagen is a structural protein found i.a... |
