OMIM - Online Mendelian Inheritance in Man

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.

OVERVIEW

The site omim.org currently has an average traffic classification of one hundred and thirteen thousand four hundred and seven (the smaller the better). We have parsed fourteen pages within the domain omim.org and found one thousand six hundred and eight websites linking to omim.org. There are three contacts and directions for omim.org to help you connect with them. There are one mass network accounts retained by this website. The site omim.org has been on the internet for one thousand two hundred and seven weeks, nineteen days, three hours, and thirty-one minutes.
Traffic Rank
#113407
Pages Parsed
14
Links to this site
1608
Contacts
3
Addresses
3
Social Links
1
Online Since
Oct 2001

OMIM.ORG TRAFFIC

The site omim.org has seen alternating amounts of traffic for the whole of the year. Hardly surprising, the site had a ranking today of one hundred and thirteen thousand four hundred and seven.
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OMIM.ORG HISTORY

The site omim.org was started on on October 03, 2001. As of today, it is one thousand two hundred and seven weeks, nineteen days, three hours, and thirty-one minutes young.
REGISTERED
October
2001

SPAN

23
YEARS
1
MONTHS
18
DAYS

LINKS TO WEBSITE

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15375 Barranca Pkwy, A105-106, Irvine CA 92618. The iGene Personal Health and Disease Risk Panel provides an invaluable health assessment to individuals in understanding their inherited and risks and preventative options in three actionable health areas that most critically shape the disease forecast of today.

Hyperlink management system

Is a tool for automatically updating and maintaining hyperlinks among major biological databases. We update correspondence tables of data IDs everyday, and provide the most up-to-date hyperlinks among databases. For details, see here. BioDBScan, an e-mail alert system of new data, was released. For details, see here.

BIOETICA PLURALIDAD Y DEBATE

LA BIOETICA EN SU DISCURSO PLURAL Y RELATIVO , SE COMPROMETE AL DEBATE Y AL CONSENSO; RESPETANDO LA AUTONOMIA Y LA DIGNIDAD DE LA PERSONA. CD DE MEXICO, D. ACADEMICO DE LA FACULTAD DE MEDICINA UNAM. MIEMBRO NUMERARIO DE LA ACADEMIA NACIONAL MEXICANA DE BIOETICA. Domingo, 11 de febrero de 2018.

WHAT DOES OMIM.ORG LOOK LIKE?

Desktop Screenshot of omim.org Mobile Screenshot of omim.org Tablet Screenshot of omim.org

CONTACTS

OMIM

JHH, Blalock 1007

Baltimore, MD, 21287

US

Joanna Amberger

JHH, Blalock 1007

Baltimore, MD, 21287

US

Verio Hostmaster

5050 Blue Lake Dr

Boca Raton, FL, 33431

US

OMIM.ORG SERVER

We observed that a single root page on omim.org took three hundred and twenty-eight milliseconds to download. Our crawlers could not detect a SSL certificate, so we consider this site not secure.
Load time
0.328 sec
SSL
NOT SECURE
IP
35.173.52.3

NAME SERVERS

ns19a.nameservers.net
ns19b.nameservers.net

WEBSITE ICON

SERVER SOFTWARE

We detected that this website is utilizing the Apache/2.2.34 (Amazon) os.

SITE TITLE

OMIM - Online Mendelian Inheritance in Man

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.

PARSED CONTENT

The site omim.org states the following, "Qtip textMIMmatch is a way to follow OMIM entries that interest you and to find other researchers who may share interest in the same entries." I noticed that the webpage also stated " A bonus to all MIMmatch users is the option to sign up for updates on new gene-phenotype relationships." They also stated " Online Mendelian Inheritance in Man. An Online Catalog of Human Genes and Genetic Disorders. Updated April 11, 2018. Require any term in your retrieval. Require all terms in your retrieval." The meta header had Mendelian Inheritance in Man as the first keyword. This keyword was followed by OMIM, Mendelian diseases, and Mendelian disorders which isn't as important as Mendelian Inheritance in Man. The other words the site used was genetic diseases. genetic disorders is also included but might not be understood by search parsers.

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