| Content | |
|---|---|
| Description | Catalog of all known human genes and genetic phenotypes. |
| Data types captured | Genes, genetic disorders, phenotypic traits |
| Organisms | Homo sapiens |
| Contact | |
| Research center | Johns Hopkins University School of Medicine |
| Primary citation | PMID 21472891 |
| Access | |
| Website | http://www.omim.org/ |
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 28 June 2019[update], approximately 9,000 of the over 25,000 entries in OMIM represented phenotypes; the rest represented genes, many of which were related to known phenotypes.[1]