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PMID: 10612823 Published · ppublish English Journal Article

Online Mendelian Inheritance in Man (OMIM).

Human mutation ·Vol. 15 ·No. 1 ·2000-00-00 ·Pages 57-61

Hamosh A, Scott AF, Amberger J, Valle D, McKusick VA

Abstract

Online Mendelian Inheritance In Man (OMIM) is a public database of bibliographic information about human genes and genetic disorders. Begun by Dr. Victor McKusick as the authoritative reference Mendelian Inheritance in Man, it is now distributed electronically by the National Center for Biotechnology Information (NCBI). Material in OMIM is derived from the biomedical literature and is written by Dr. McKusick and his colleagues at Johns Hopkins University and elsewhere. Each OMIM entry has a full text summary of a genetic phenotype and/or gene and has copious links to other genetic resources such as DNA and protein sequence, PubMed references, mutation databases, approved gene nomenclature, and more. In addition, NCBI's neighboring feature allows users to identify related articles from PubMed selected on the basis of key words in the OMIM entry. Through its many features, OMIM is increasingly becoming a major gateway for clinicians, students, and basic researchers to the ever-growing literature and resources of human genetics.

MeSH Terms
Alleles Databases, Factual Genetics Genetics, Medical Humans
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Hamosh A
McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21287, USA.
Scott A F
Amberger J
Valle D
McKusick V A
Article Info
Journal
Human mutation
Abbr.
Hum Mutat
ISSN
1059-7794
Published
2000-00-00
Pages
57-61
Language
English
Region
United States
NLM ID
9215429
Subset
IM
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