aniridia.net

Aniridia Foundation International

501c3 nonprofit supporting people with aniridia syndrome, a genetic condition of underdeveloped eye structures, with research and education
history traffic contact

OVERVIEW

This website aniridia.net presently has an average traffic classification of zero (the lower the more traffic). We have explored six pages inside the web page aniridia.net and found sixty-nine websites associating themselves with aniridia.net. There is one contacts and locations for aniridia.net to help you contact them. There is three public media sites linked to aniridia.net. This website aniridia.net has been online for one thousand two hundred and nine weeks, seven days, twelve hours, and sixteen minutes.
Pages Crawled
6
Links to this site
69
Contacts
1
Locations
1
Social Links
3
Online Since
Mar 2001

ANIRIDIA.NET RANKINGS

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ANIRIDIA.NET HISTORY

This website aniridia.net was first submitted to the registrar on March 13, 2001. This domain was last updated on the date of March 13, 2014. This site will expire on the date of March 13, 2015. It is currently one thousand two hundred and nine weeks, seven days, twelve hours, and sixteen minutes old.
REGISTERED
March
2001
UPDATED
March
2014
EXPIRED
March
2015

LENGTH OF LIFE

23
YEARS
2
MONTHS
7
DAYS

LINKS TO WEB SITE

American Association for Pediatric Ophthalmology and Strabismus

American Association for Pediatric Ophthalmology and Strabismus. A Comprehensive Approach to Vertical Strabismus Webinar. What is strabismus and how common is it? Strabismus is any misalignment of the eyes. What should be done if a child. Has an eye injury? .

Aniridi Norge

Er en landsdekkende interesseorganisasjon for mennesker med den sjeldne diagnosen aniridi. Bidra til at alle med aniridi får god informasjon, den beste behandlingen, og inspirere til forskning gjennom internasjonalt samarbeid. Her er saksliste og andre årsmøtepapirer til årsmøtet 2015. Hjelp, jeg skal snart bli mamma til en i 1. klasse! 18 mar, 2015.

Aniridia Italiana Il portale dellassociazione

Dal 22 al 24 novembre 201.

Aniridia Network UK Supporting people with aniridia and their families

Supporting people with aniridia and their families. Running for fun and aniridia. How we spend the money you raise? Aniridia around the world. We are a support group and charity concerned with the rare genetic condition aniridia. Our next conference will be in Newcastle in autumn 2015.

I AM POTENTIAL

Friday, January 30, 2015. Wednesday, December 31, 2014. Monday, December 1, 2014. Friday, November 14, 2014. Friday, October 31, 2014. 101 Mobility Halloween Wheelchair Costume Parade at Codington Elementary! Monday, October 27, 2014. Friday, October 24, 2014.

Untukmu, anak-anakku.

Rabu, 16 Oktober 2013. Kamis, 10 Oktober 2013. What a Day, Beb. Hari ini cek pertama kaka .

WHAT DOES ANIRIDIA.NET LOOK LIKE?

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CONTACTS

ANIRIDIA FOUNDATION INTERNATIONAL

JILL NERBY

2104 ARLINGTON BLVD

CHARLOTTESVILLE, VA, 22903

US

43.42433357
packrena@aol.com

ANIRIDIA.NET HOST

I found that a lone root page on aniridia.net took five thousand four hundred and thirteen milliseconds to come up. We could not observe a SSL certificate, so therefore our web crawlers consider aniridia.net not secure.
Load time
5.413 secs
SSL
NOT SECURE
Internet Protocol
108.167.135.116

NAME SERVERS

ns-us.1and1-dns.com
ns-us.1and1-dns.de
ns-us.1and1-dns.org
ns-us.1and1-dns.us

SERVER OS AND ENCODING

I diagnosed that aniridia.net is employing the Microsoft-IIS/7.5 operating system.

PAGE TITLE

Aniridia Foundation International

DESCRIPTION

501c3 nonprofit supporting people with aniridia syndrome, a genetic condition of underdeveloped eye structures, with research and education

CONTENT

This website has the following in the web page, "Website Designed at Homestead List Your Business for Free." We viewed that the web site also stated " For some, your journey has just started, and others have a whole life full of experiences." It also said " Either way, you will be able to learn and share many things through Aniridia Foundation International. The core of AFI is centered on. You are not alone and we are here to help! We welcome you to join us and see how our team efforts can assist the low vision community, make advancements in research, improve patient care and one day, a cure." The header had 1and1 as the highest ranking search term. It is followed by domain, domain name, and domain name registration which isn't as ranked as highly as 1and1. The next words they uses is mywebsite. web site was included and will not be seen by web crawlers.

VIEW SUBSEQUENT WEB PAGES

Aniridia Network UK Supporting people with aniridia and their families

Supporting people with aniridia and their families. Running for fun and aniridia. How we spend the money you raise? Aniridia around the world. We are a support group and charity concerned with the rare genetic condition aniridia. Our next conference will be in Newcastle in autumn 2015.

Seeing what cannot be seen. The Struggle to Med School

The Struggle to Med School. May 5, 2009 in Random Thoughts. Try and see how your words and actions are seen by those around you. April 2, 2009 in Random Thoughts.

ANIRIDIA HABLA HISPANA O LATINOS

Sábado, 10 de marzo de 2012. Lunes, 5 de marzo de 2012. Otra más interna, mucoacuosa.

AWS - Aniridie-Wagr e.V.

Ist eine seltene genetisch bedingte Fehlbildung des Sehorgans welches sehr komplexe Auswirkungen auf die Entwicklung hat. Dadurch kann die Pupille sich nicht schließen und nicht das einfallende Licht regulieren.