europe omim.org

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.
traffic

OVERVIEW

The site europe.omim.org currently has an average traffic classification of zero (the smaller the better). We have parsed zero pages within the domain europe.omim.org and found one website linking to europe.omim.org. There are one mass network accounts retained by this website.
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EUROPE.OMIM.ORG TRAFFIC

The site europe.omim.org has seen alternating amounts of traffic for the whole of the year.
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LINKS TO WEBSITE

OMIM - Online Mendelian Inheritance in Man

A bonus to all MIMmatch users is the option to sign up for updates on new gene-phenotype relationships. Online Mendelian Inheritance in Man. An Online Catalog of Human Genes and Genetic Disorders. And Online Mendelian Inheritance in Man.

WHAT DOES EUROPE.OMIM.ORG LOOK LIKE?

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EUROPE.OMIM.ORG SERVER

We observed that a single root page on europe.omim.org took one thousand one hundred and seventy-seven milliseconds to download. Our crawlers could not detect a SSL certificate, so we consider this site not secure.
Load time
1.177 sec
SSL
NOT SECURE
IP
193.62.197.14

SERVER SOFTWARE

We detected that this website is utilizing the Apache/2.2.15 (CentOS) 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 europe.omim.org states the following, "A bonus to all MIMmatch users is the option to sign up for updates on new gene-phenotype relationships." I noticed that the webpage also stated " Online Mendelian Inheritance in Man." They also stated " An Online Catalog of Human Genes and Genetic Disorders. Require any term in your retrieval. Require all terms in your retrieval. Require some terms in your retrieval. Require phrases and terms in your retrieval. And Online Mendelian Inheritance in Man." 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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Monday, May 4 2009. Kurasakan ku jatuh cinta sejak pertama berjumpa. Senyumanmu yang selalu menghiasi hariku. Kau ciptaanNya yang terindah, yang menghanyutkan hatiku. Semua telah terjadi, aku tak bisa berhenti memikirkanmu. Kau yang kuinginkan meski tak kuungkapkan. Kau yang kubayangkan yang slalu kuimpikan. Aku jatuh cinta, tlah jatuh cinta. Cinta kepadamu, ku jatuh cinta. Tuesday, Apr 28 2009. OJO LALI YO REK! .