Databases > DOI:10.25504/FAIRsharing.9qkaz9

ready Online Mendelian Inheritance in Man

Abbreviation:OMIM

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General Information
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. It is updated daily, and the entries contain copious links to other genetics resources.

How to cite this record: FAIRsharing.org: OMIM; Online Mendelian Inheritance in Man; DOI: https://doi.org/10.25504/FAIRsharing.9qkaz9; Last edited: Feb. 22, 2018, 3 p.m.; Last accessed: Apr 20 2018 4:12 a.m.



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Record added: April 20, 2016, 8:58 p.m.
Record updated: Jan. 16, 2018, 10:47 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 Paper (DOI)

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 Paper (DOI)