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1. www.omim.orgHome - OMIM

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   3 days ago · 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.

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2. en.wikipedia.org › wiki › Mendelian_traits_in_humansMendelian traits in humans - Wikipedia

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   Mendelian traits in humans are human traits that are substantially influenced by Mendelian inheritance. Most – if not all – Mendelian traits are also influenced by other genes, the environment, immune responses, and chance. Therefore no trait is purely Mendelian, but many traits are almost entirely Mendelian, including canonical examples ...

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   What is Online Mendelian inheritance in man?

   • Make a donation! 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.

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   What is Mendelian inheritance in Man (OMIM)?

   • The Online Mendelian Inheritance in Man (OMIM) database currently lists 6,209 single gene disorders and traits (updated 8 November 2022), and these represent more than 70% of the ‘rare diseases’ (conditions with a prevalence of <1:2,000) that, in total, are estimated to affect 4–5% of the global general population 6.

   Mendelian inheritance revisited: dominance and recessiveness ... - Nature

   www.nature.com/articles/s41576-023-00574-0

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   Who owns OMIM ® & Online Mendelian inheritance in man ®?

   • OMIM ® and Online Mendelian Inheritance in Man ® are registered trademarks of the Johns Hopkins University. Copyright ® 1966-2024 Johns Hopkins University. NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine.

   About OMIM - OMIM

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   What is Mendelian inheritance in Man (MIM)?

   • This database was initiated in the early 1960s by Dr. Victor A. McKusick as a catalog of mendelian traits and disorders, entitled Mendelian Inheritance in Man (MIM). Twelve book editions of MIM were published between 1966 and 1998.

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4. en.wikipedia.org › wiki › Mendelian_inheritanceMendelian inheritance - Wikipedia

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   Mendelian inheritance (also known as Mendelism) is a type of biological inheritance following the principles originally proposed by Gregor Mendel in 1865 and 1866, re-discovered in 1900 by Hugo de Vries and Carl Correns, and later popularized by William Bateson.

5. en.wikipedia.org › wiki › Online_MendelianOnline Mendelian Inheritance in Man - Wikipedia

   en.wikipedia.org › wiki › Online_Mendelian

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   Online Mendelian Inheritance in Man; Content; Description: Catalog of all known human genes and genetic phenotypes. Data types captured: Genes, genetic disorders, phenotypic traits: Organisms: Homo sapiens: Contact; Research center: Johns Hopkins University School of Medicine: Primary citation: PMID 21472891: Access; Website: http://www.omim.org/

   • Description: Catalog of all known human genes and genetic phenotypes.
   • Research center: Johns Hopkins University School of Medicine

   • Organisms: Homo sapiens

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     An Introduction to Mendelian Genetics | Biomolecules | MCAT | Khan Academy

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7. www.nature.com › articles › s41576/023/00574-0Mendelian inheritance revisited: dominance and recessiveness ...

   www.nature.com › articles › s41576/023/00574-0

   Feb 20, 2023 · The Online Mendelian Inheritance in Man (OMIM) database currently lists 6,209 single gene disorders and traits (updated 8 November 2022), and these represent more than 70% of the ‘rare...

8. academic.oup.com › nar › articleOMIM.org: Online Mendelian Inheritance in Man (OMIM®), an ...

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   Nov 26, 2014 · INTRODUCTION. Online Mendelian Inheritance in Man (OMIM), a continuation of Dr Victor A. McKusick's Mendelian Inheritance in Man (MIM) ( 1 ), is the primary repository of comprehensive, curated information on genes and genetic phenotypes and the relationships between them.