Last Updated: Oct 15, 2018 12:27 PM
Connect to Database
This database is freely available to the general public via the Internet.
Online Mendelian Inheritance in Man (OMIM® is a continuously updated catalog of human genes and genetic disorders and traits, with particular focus on the molecular relationship between genetic variation and phenotypic expression. It is considered to be a phenotypic companion to the Human Genome Project. OMIM is currently biocurated at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine. Although you may still search OMIM through NCBI (http://www.ncbi.nlm.nih.gov/omim), the regularly updated database and full range of search functions are now maintained at omim.org.
MIM first published in 1966; OMIM updates are frequent.
Mendelian Inheritance in Man: Catalog of Autosomal Dominant, Autosomal Recessive, and X-linked Phenotypes
Health Sciences Library
CALL NUMBER: HSL Ref ZQZ 50 M159m