| Display title | Biology:Online Mendelian Inheritance in Man |
| Default sort key | Online Mendelian Inheritance in Man |
| Page length (in bytes) | 9,732 |
| Namespace ID | 3026 |
| Namespace | Biology |
| Page ID | 460951 |
| 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>Nautica |
| Date of page creation | 12:47, 10 February 2024 |
| Latest editor | imported>Nautica |
| Date of latest edit | 12:47, 10 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. | Online Mendelian Inheritance in Man (OMIM) is a continuously updated catalog of human genes and genetic disorders and traits, with a particular focus on the gene-phenotype relationship. (As of June 2019), approximately 9,000 of the over 25,000 entries in OMIM represented phenotypes; the rest represented... |
