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McKusick's Online Mendelian Inheritance in Man (OMIM®)

McKusick's Online Mendelian Inheritance in Man (OMIM®; http://www.ncbi.nlm.nih.gov/omim), a knowledgebase of human genes and phenotypes, was originally published as a book, Mendelian Inheritance in Man, in 1966. The content of OMIM is derived exclusively from the published biomedical literature...

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Detalles Bibliográficos
Autores principales: Amberger, Joanna, Bocchini, Carol A., Scott, Alan F., Hamosh, Ada
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2686440/
https://www.ncbi.nlm.nih.gov/pubmed/18842627
http://dx.doi.org/10.1093/nar/gkn665
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author Amberger, Joanna
Bocchini, Carol A.
Scott, Alan F.
Hamosh, Ada
author_facet Amberger, Joanna
Bocchini, Carol A.
Scott, Alan F.
Hamosh, Ada
author_sort Amberger, Joanna
collection PubMed
description McKusick's Online Mendelian Inheritance in Man (OMIM®; http://www.ncbi.nlm.nih.gov/omim), a knowledgebase of human genes and phenotypes, was originally published as a book, Mendelian Inheritance in Man, in 1966. The content of OMIM is derived exclusively from the published biomedical literature and is updated daily. It currently contains 18 961 full-text entries describing phenotypes and genes. To date, 2239 genes have mutations causing disease, and 3770 diseases have a molecular basis. Approximately 70 new entries are added and 700 entries are updated per month. OMIM® is expanding content and organization in response to shifting biological paradigms and advancing biotechnology.
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spelling pubmed-26864402009-05-26 McKusick's Online Mendelian Inheritance in Man (OMIM®) Amberger, Joanna Bocchini, Carol A. Scott, Alan F. Hamosh, Ada Nucleic Acids Res Articles McKusick's Online Mendelian Inheritance in Man (OMIM®; http://www.ncbi.nlm.nih.gov/omim), a knowledgebase of human genes and phenotypes, was originally published as a book, Mendelian Inheritance in Man, in 1966. The content of OMIM is derived exclusively from the published biomedical literature and is updated daily. It currently contains 18 961 full-text entries describing phenotypes and genes. To date, 2239 genes have mutations causing disease, and 3770 diseases have a molecular basis. Approximately 70 new entries are added and 700 entries are updated per month. OMIM® is expanding content and organization in response to shifting biological paradigms and advancing biotechnology. Oxford University Press 2009-01 2008-10-08 /pmc/articles/PMC2686440/ /pubmed/18842627 http://dx.doi.org/10.1093/nar/gkn665 Text en © 2008 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Amberger, Joanna
Bocchini, Carol A.
Scott, Alan F.
Hamosh, Ada
McKusick's Online Mendelian Inheritance in Man (OMIM®)
title McKusick's Online Mendelian Inheritance in Man (OMIM®)
title_full McKusick's Online Mendelian Inheritance in Man (OMIM®)
title_fullStr McKusick's Online Mendelian Inheritance in Man (OMIM®)
title_full_unstemmed McKusick's Online Mendelian Inheritance in Man (OMIM®)
title_short McKusick's Online Mendelian Inheritance in Man (OMIM®)
title_sort mckusick's online mendelian inheritance in man (omim®)
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2686440/
https://www.ncbi.nlm.nih.gov/pubmed/18842627
http://dx.doi.org/10.1093/nar/gkn665
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