- Enter one or more search terms.
- Use Limits to restrict your search by search field, chromosome, and other
criteria.
- Use Index to browse terms found in OMIM records.
- Use History to retrieve records from previous searches, or to combine
searches.
NCBI is implementing changes to help you find current content in OMIM based on resources at NCBI, and then directing you to
omim.org. Please be aware that you will leave NCBI to view OMIM records. Access to full records from NCBI (e.g. web, ftp, eutils) will no longer be supported.
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OMIM
®
- Online Mendelian Inheritance in Man
®
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Welcome to OMIM
®
, Online Mendelian Inheritance in Man
®
. OMIM is 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.
This database was initiated in the early 1960s by Dr. Victor A. McKusick as a catalog of
mendelian traits and disorders, entitled Mendelian Inheritance in Man (MIM). Twelve book
editions of MIM were published between 1966 and 1998. The online version, OMIM, was created
in 1985 by a collaboration between the National Library of Medicine and the William H. Welch
Medical Library at Johns Hopkins. It was made generally available on the internet starting
in 1987. In 1995, OMIM was developed for the World Wide Web by NCBI, the National Center for
Biotechnology Information.
OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns
Hopkins University School of Medicine, under the direction of Dr. Ada Hamosh.
NLM's Profiles in Science -- The McKusick Papers More...
NOTE: OMIM is intended for use primarily by physicians and other professionals concerned
with genetic disorders, by genetics researchers, and by advanced students in science and
medicine. While the OMIM database is open to the public, users seeking information about a
personal medical or genetic condition are urged to consult with a qualified physician for
diagnosis and for answers to personal questions.
OMIM
®
and Online Mendelian Inheritance in Man
®
are registered trademarks of the Johns Hopkins University.