OMIM - Online Mendelian Inheritance in Man

Web Name: OMIM - Online Mendelian Inheritance in Man

WebSite: http://www.omim.org

ID:246533

Keywords:

Mendelian,Online,OMIM,Man,in,Inheritance,MendelianInheritanceinMan,OMIM,Mendelia

Description:

keywords:Mendelian Inheritance in Man, OMIM, Mendelian diseases, Mendelian disorders, genetic diseases, genetic disorders, genetic disorders in humans, genetic phenotypes, phenotype and genotype, disease models, alleles, genes, dna, genetics, dna testing, gene testing, clinical synopsis, medical genetics
description: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. It is updated daily, and the entries contain copious links to other genetics resources.
OMIM Online Mendelian Inheritance in Man An Online Catalog of Human Genes and Genetic Disorders Updated November 22, 2021

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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. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.
OMIM and Online Mendelian Inheritance in Man are registered trademarks of the Johns Hopkins University.
Copyright 1966-2021 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. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.
OMIM and Online Mendelian Inheritance in Man are registered trademarks of the Johns Hopkins University.
Copyright 1966-2021 Johns Hopkins University.
Printed: Nov. 23, 2021 OMIM Donation:

Dear OMIM User,

To ensure long-term funding for the OMIM project, we have diversified our revenue stream. We are determined to keep this website freely accessible. Unfortunately, it is not free to produce. Expert curators review the literature and organize it to facilitate your work. Over 90% of the OMIM's operating expenses go to salary support for MD and PhD science writers and biocurators. Please join your colleagues by making a donation now and again in the future. Donations are an important component of our efforts to ensure long-term funding to provide you the information that you need at your fingertips.

Thank you in advance for your generous support,
Ada Hamosh, MD, MPH
Scientific Director, OMIM

TAGS:Mendelian Online OMIM Man in Inheritance MendelianInheritanceinMan OMIM Mendelia

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

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