Home Page - FDMAS Patient Registry

FDMAS Patient Registry registry powered by NORD platform.

OVERVIEW

The site fdmasregistry.org presently has a traffic classification of zero (the smaller the higher page views). We have inspected two pages within the web site fdmasregistry.org and found one website referring to fdmasregistry.org. We were able to detect two contacts and directions for fdmasregistry.org to help you connect with them. The site fdmasregistry.org has been online for five hundred and ninety-four weeks, twenty-one days, nineteen hours, and forty-five minutes.
Pages Crawled
2
Links to this site
1
Contacts
2
Addresses
2
Online Since
Jul 2013

FDMASREGISTRY.ORG TRAFFIC

The site fdmasregistry.org is seeing fluctuating amounts of traffic within the past the year.
Traffic for fdmasregistry.org

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FDMASREGISTRY.ORG HISTORY

The site fdmasregistry.org was first documented on July 23, 2013. It is now five hundred and ninety-four weeks, twenty-one days, nineteen hours, and forty-five minutes young.
REGISTERED
July
2013

DOMAIN PERIOD OF EXISTANCE

11
YEARS
4
MONTHS
20
DAYS

LINKS TO DOMAIN

WHAT DOES FDMASREGISTRY.ORG LOOK LIKE?

Desktop Screenshot of fdmasregistry.org Mobile Screenshot of fdmasregistry.org Tablet Screenshot of fdmasregistry.org

CONTACTS

Lisa Heral

Lisa Heral

Fibrous Dysplasia Foundation

Washington DC, DC, 20003

US

Lunarpages

System Administrator

1360 N. Hancock St

Anaheim, CA, 92807

US

FDMASREGISTRY.ORG SERVER

We revealed that a lone root page on fdmasregistry.org took one thousand three hundred and twenty-two milliseconds to download. We found a SSL certificate, so in conclusion our crawlers consider fdmasregistry.org secure.
Load time
1.322 secs
SSL
SECURE
Internet Protocol
23.96.96.142

NAME SERVERS

ns1.lunarpages.com
ns2.lunarpages.com

SERVER OS

We detected that fdmasregistry.org is operating the Microsoft-IIS/8.0 os.

HTML TITLE

Home Page - FDMAS Patient Registry

DESCRIPTION

FDMAS Patient Registry registry powered by NORD platform.

PARSED CONTENT

The site states the following, "The Fibrous DysplasiaMcCune-Albright Syndrome Patient Registry Your story powers research! Learn more." We noticed that the web site stated " This is a unique rare disease patient registry." It also stated " Are you interested in using our data to further your rare disease research? Participating in This Study. Information collected during this study may be used to help provide opportunities for patients and researchers to collaborate in the rare disaease community. Please create an account and provide consent to participate in the study."

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