OMIM is a comprehensive, searchable compendium of human genes and genetic phenotypes that is freely available and updated daily.
Website presents a comprehensive, authoritative, and timely compendium of human genes and genetic phenotypes. The full-text, referenced overviews in OMIM contain information on all known mendelian disorders and over 12,000 genes. OMIM focuses on the relationship between phenotype and genotype. It is updated daily, and the entries contain copious links to other genetics resources.
|Note||Website database; Continuously updated; reference material|
|Date of Resource||2019|
Experts from the disciplines listed below have tagged this resource as fulfulling genomic competencies.