OMIM - Online Mendelian Inheritance in Man
Time 2021-11-23 23:42:37Web Name: OMIM - Online Mendelian Inheritance in Man
WebSite: http://www.omim.org
ID:246533
Keywords:
Mendelian,Online,OMIM,Man,in,Inheritance,MendelianInheritanceinMan,OMIM,MendeliaDescription:
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, 2021Advanced Search : OMIM, Clinical Synopses, Gene Map
Need help? : Example Searches" qtip_text=" Require any term in your retrieval: clinodactyly or hypertelorism clinodactyly hypertelorism Require all terms in your retrieval: clinodactyly and hypertelorism +clinodactyly +hypertelorism Require some terms in your retrieval: clinodactyly not hypertelorism +clinodactyly -hypertelorism Require phrases in your retrieval: short stature and clinodactyly +short stature +clinodactyly ">Example Searches, OMIM Search Help, OMIM Video Tutorials
Mirror site : https://mirror.omim.org
OMIM is supported by a grant from NHGRI, licensing fees, and generous contributions from people like you.
Make a donation!
Follow us on Twitter
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
<<< Thank you for your visit >>>
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.Websites to related : XT Xing Technologies – Quality
keywords:
description:
CALL US+65-6778-5773
+86-20-3938-8151EMAIL USsales@xtxingtech.comHomeAbout UsProducts ServicesAccreditationsContact Usdeliver
keywords:
description:
Homenew here?work with me rev-o-rama sonic vroom mojo, yo resultsbuy stuff teletastical archives remembering through resonancef
keywords:
description:
Themain issues
HumanRights
Death penalty Condom ban Poverty
keywords:
description:Internships and Jobs on and off Capitol Hill in Washington, DC
HillZoo.com - The Home Page of Capitol HillCapitol Hill Internshi
keywords:automated plating equipment, PCB plating lines, PCB plating equipment, solar panel plating equipment, solar panel plating machinery, circuit
Coastal Air Inc. - Flight Schoolkeywords:flight training CT, private pilot license, flight school CT, instrument rating, private pilot, commercial pilot, pilot training, aircraft ren
Olympic Peninsula Region Porsch keywords:
description:
Olympic Peninsula Region Porsche Club of America Skip to content HomeAbout Le
keywords:
description:
Copper Beech Institute ONLINE OFFERINGS
keywords:
description:
ip-address.comHomeMy IPSpeedtestSitemapProxy CheckerProxy ListVerify Email AddressTrace Email AddressIP to Zip CodeIP Address D
keywords:
description:Sequence - The database for the token economy.
Hot Websites