BioPontis Alliance for rare diseases

for rare diseases

OVERVIEW

The domain biopontisalliance.org currently has an average traffic classification of zero (the lower the more users). We have parsed three pages within the domain biopontisalliance.org and found four websites linking to biopontisalliance.org. There are three public web sites enjoyed by biopontisalliance.org.
Pages Parsed
3
Links to this site
4
Social Links
3

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The domain biopontisalliance.org has seen variant levels of traffic for the whole of the year.
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LINKS TO WEBSITE

MLD Foundation Blog - Musings about MLD and rare disease policyMLD Foundation Blog Musings about MLD and rare disease policy

Musings about MLD and rare disease policy. Registration for our 2105 MLD Family Conference. In Newark Delaware is underway and closes in just a couple of weeks. Many of your MLD Family will be there. To meet, share, and socialize with. If you need some help.

WHAT DOES BIOPONTISALLIANCE.ORG LOOK LIKE?

Desktop Screenshot of biopontisalliance.org Mobile Screenshot of biopontisalliance.org Tablet Screenshot of biopontisalliance.org

BIOPONTISALLIANCE.ORG SERVER

I observed that a single root page on biopontisalliance.org took five thousand three hundred and thirteen milliseconds to come up. Our web crawlers could not observe a SSL certificate, so in conclusion our web crawlers consider this site not secure.
Load time
5.313 sec
SSL
NOT SECURE
IP
206.188.193.231

SERVER SOFTWARE

We observed that this website is using the Apache/2.2.29 (Unix) FrontPage/5.0.2.2635 operating system.

SITE TITLE

BioPontis Alliance for rare diseases

DESCRIPTION

for rare diseases

PARSED CONTENT

The domain biopontisalliance.org has the following in the web page, "The Tragedy of Rare Diseases." I analyzed that the webpage also stated " Childhood should be a time of joy, wonder and hope for the future." They also stated " For families of children with a rare, serious disease, it can be frustrating, painful and frightening. It can include a long journey to countless doctor visits over many years to finally arrive at a diagnosis, only to find there is no treatment available. Over 7000 rare diseases are known. Tragically, there are no effective treatments for most, 95, of rare diseases."

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