OMIM

OMIM (Online Mendelian Inheritance in Man) is a comprehensive and continuously updated database that catalogs human genes and genetic disorders. Originally developed by Dr. Victor McKusick in 1966, OMIM serves as a critical resource for researchers, clinicians, and educators in the field of genetics and medicine. The database offers detailed entries for each gene and disorder, including information on their inheritance patterns, clinical features, molecular mechanisms, and related literature. OMIM is widely used to support genetic research, facilitate clinical diagnosis, and enhance understanding of genetic contributions to diseases. Key features of OMIM include: Extensive Gene and Disorder Catalog: OMIM contains entries for over 15,000 genes and more than 7,000 genetic disorders, providing a wealth of information for both common and rare conditions. Research Integration: The database links genetic data with clinical findings, allowing users to explore the relationships between genes and health outcomes. User-Friendly Interface: OMIM is designed for easy navigation, enabling users to search for specific genes, disorders, or keywords efficiently. Regular Updates: The database is continuously updated to reflect new research findings, ensuring that users have access to the latest information in the rapidly evolving field of genetics. Overall, OMIM is an invaluable tool for advancing the understanding of genetic diseases and their implications in human health.