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Online Mendelian Inheritance in Man OMIM

Online

A comprehensive, authoritative and timely research resource of curated descriptions of human genes and phenotypes and the relationships between them. OMIM® is based on the published peer-reviewed biomedical literature and is used by overlapping and diverse communities of clinicians, molecular biologists and genome scientists, as well as by students and teachers of these disciplines. Genes and phenotypes are described in separate entries and are given unique, stable six-digit identifiers (MIM numbers). OMIM® entries have a structured free-text format that provides the flexibility necessary to describe the complex and nuanced relationships between genes and genetic phenotypes in an efficient manner.

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OMIM classification

  • Animals
    • Homo sapiens

OMIM specifications

Restrictions to use:
None
Data access:
File download, Browse, Application programming interface
Maintained:
Yes
Community driven:
No
User data submission:
Not allowed

OMIM distribution

OMIM support

Documentation

Maintainer

  • Joan S. Amberger <>

Credits

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Publications

Institution(s)

McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA; FS Consulting, Salem, MA, USA

Funding source(s)

National Human Genome Research Institute [1U41HG006627]

Link to literature

By using OMICtools you acknowledge that you have read and accepted the terms of the end user license agreement.