Back Online Mendelian Inheritance in Man Afrikaans الوراثة المندلية البشرية عبر الإنترنت Arabic OMIM Azerbaijani OMIM Bulgarian OMIM BS Mendelian Inheritance in Man Catalan Online Mendelian Inheritance in Man Welsh Mendelian Inheritance in Man Danish Online Mendelian Inheritance in Man German Μεντελική Κληρονομικότητα του Ανθρώπου στο Διαδίκτυο Greek
| 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]
- ^ "OMIM Entry Statistics". Online Mendelian Inheritance in Man. Baltimore, MD: McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University. 2019. Retrieved 28 June 2019.
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