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Websites, domains, hosts that links to irdirc.org

Our database shows, that the website irdirc.org is linked by a total of 7 websites.

 
Number of websites/domains displayed: 7
Results found: 7
 

Websites discovered:

The Golden Helix Foundation - Home
http://pageoverview.com/website-report/goldenhelix.org
  • Expected expiration: June 10th in 2019
  • Creation date: June 10th in 2004
  • Renew date: September 3rd in 2017
  • Google Analytics: 23923132-32
Home | Human Phenotype Ontology
http://pageoverview.com/website-report/human-phenotype-ontology.github.io
Homepage for the Human Phenotype Ontology Project and related resources.
  • Google Analytics: 62837903-6
Home - Matchmaker Exchange
http://pageoverview.com/website-report/matchmakerexchange.org
Home - Matchmaker Exchange
  • Expected expiration: April 28th in 2018
  • Creation date: April 28th in 2014
  • Renew date: April 28th in 2017
  • Google Analytics: 55846925-1
IRDiRC – International Rare Diseases Research Consortium
http://pageoverview.com/website-report/irdirc.org
  • Expected expiration: May 28th in 2022
  • Creation date: May 28th in 2012
  • Renew date: November 15th in 2017
  • Google Analytics: 42329332-1
中国国家罕见病注册体系
http://pageoverview.com/website-report/nrdrs.org
中国首个国家级罕见病注册平台,“十三五”重点项目,为广大罕见病研究者提供一个权威、可靠的共享平台。
  • Expected expiration: November 25th in 2019
  • Creation date: November 25th in 2016
  • Renew date: June 1st in 2017
Centre de référence des Maladies Vasculaires Rares - APHP
http://pageoverview.com/website-report/maladies-vasculaires-rares.fr
Le CRMVR regroupe 39 hôpitaux et centres de compétence en France et permet l'accueil et le traitement des patients atteints de maladies vasculaires rares.
  • Google Analytics: 80836311-1
OMIM - Online Mendelian Inheritance in Man
http://pageoverview.com/website-report/omim.org
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.
  • Expected expiration: October 3rd in 2017
  • Creation date: October 3rd in 2001
  • Renew date: July 9th in 2016
  • Google Analytics: 20344157-1
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