databases > DOI:10.25504/FAIRsharing.9qkaz9
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ready Online Mendelian Inheritance in Man

Abbreviation:OMIM

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General Information
Online Mendelian Inheritance in Man (OMIM) is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily. The full-text, referenced overviews in OMIM contain information on all known mendelian disorders and over 15,000 genes. OMIM focuses on the relationship between phenotype and genotype.

Homepage https://omim.org/

Countries that developed this resource United States

Created in 1966

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How to cite this record FAIRsharing.org: OMIM; Online Mendelian Inheritance in Man; DOI: https://doi.org/10.25504/FAIRsharing.9qkaz9; Last edited: March 18, 2021, 11:46 a.m.; Last accessed: Oct 19 2021 12:15 p.m.


Record added: April 20, 2016, 8:58 p.m.
Record updated: March 18, 2021, 11:45 a.m. by The FAIRsharing Team.

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Publications

Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders.

Hamosh A,Scott AF,Amberger JS,Bocchini CA,McKusick VA
Nucleic Acids Res 2004

View Paper (PubMed) View Publication

OMIM.org: Online Mendelian Inheritance in Man (OMIM(R)), an online catalog of human genes and genetic disorders.

Amberger JS,Bocchini CA,Schiettecatte F,Scott AF,Hamosh A
Nucleic Acids Res 2014

View Paper (PubMed) View Publication

OMIM.org: leveraging knowledge across phenotype-gene relationships.

Amberger JS,Bocchini CA,Scott AF,Hamosh A
Nucleic Acids Res 2018

View Paper (PubMed) View Publication

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  • NHGRI 1U41HG006627 (National Institutes of Health (NIH), Bethesda, MD, USA)