| Display title | Medicine:Mevalonate kinase deficiency |
| Default sort key | Mevalonate kinase deficiency |
| Page length (in bytes) | 18,297 |
| Namespace ID | 3048 |
| Namespace | Medicine |
| Page ID | 531745 |
| Page content language | en - English |
| Page content model | wikitext |
| Indexing by robots | Allowed |
| Number of redirects to this page | 2 |
| 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>WikiGary |
| Date of page creation | 22:21, 7 February 2024 |
| Latest editor | imported>WikiGary |
| Date of latest edit | 22:21, 7 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. | Mevalonate kinase deficiency (MKD) is an autosomal recessive metabolic disorder that disrupts the biosynthesis of cholesterol and isoprenoids. It is a very rare genetic disease.
It is characterized by an elevated level of immunoglobulin D in the blood.
Mevalonate kinase (MVK) is an enzyme involved in... |
