last data update: 2011/10/18, 03:11

Website loading time

during the test: 0.33 s

cable connection (average): 0.46 s

DSL connection (average): 0.59 s

modem (average): 7.45 s

HTTP headers

Information about DNS servers

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Received from the first DNS server

Received from the second DNS server

Request to the server "rarediseases.org"
Received 34 bytes from address 211.100.21.184#53 in 530 ms
Request to the server "rarediseases.org"
You used the following DNS server:
DNS Name: ns1.halade.com
DNS Server Address: 211.100.21.184#53
DNS server aliases:

Host rarediseases.org not found: 5(REFUSED)
Received 34 bytes from address 211.100.21.184#53 in 531 ms

Subdomains (the first 50)

Typos (misspells)

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Location

IP: 64.246.135.85

continent: NA, country: United States (USA), city: Albany

Website value

rank in the traffic statistics:

There is not enough data to estimate website value.

Basic information

website build using CSS

code weight: 49.85 KB

text per all code ratio: 31 %

title: Welcome to NORD — National Organization for Rare Disorders

description:

keywords:

encoding: utf-8

language: en

Website code analysis

one word phrases repeated minimum three times

PhraseQuantity
NORD25
and23
for19
More19
to18
the16
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in11
on10
Patient10
of9
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FDA9
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two word phrases repeated minimum three times

PhraseQuantity
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three word phrases repeated minimum three times

PhraseQuantity
More news News4
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B tags

NORD Releases Landmark Study of FDA Orphan Drug Approvals

13 New Compassionate Allowances!

1st Annual US Conference on Rare Diseases and Orphan Products

Rao To Serve as OOPD Acting Director

Help NORD Support New Caucus

Appealing Insurance Denials Often A Good Course

Next PNH Meeting to be in Los Angeles

on October 15

Thank You for Supporting Rare Disease Day 2011

The PMP Research Foundation responds to NY Times Article

NORD To Host Meeting for Members in New York

FDA Seeks Nominations for Advisory Committees

The National Foundation for Ectodermal Dysplasias (NFED) Announces New ED

Congenital Cyanotic Heart Disease (CCHD) Recommended for Uniform Newborn Screening Panel

FDA/ DIA Designation Workshops Planned for VA and London

NIH Seeks Public Common Fund Input

Pediatric Device Grant Awards Announced

NORD Comments on PDUFA Draft

New Program to Help Start-ups License NIH Biomedical Patents

Message To Congress: Give FDA Funds It Needs

Commissioner in WSJ: FDA Remains Gold Standard

NORD Submits Citizen's Petition

...to the FDA, requesting a policy on rare diseases and orphan drugs.  More >NORD and Advocacy Partners Submit Risk Letters

Caring for Carcinoid Foundation

Amyloidosis Support Groups

U tags

I tags

Wall Street Journal

images

file namealternative text
Alone we are rare. Together we are strong.
slide_001.jpg
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slide_003.jpg
slide_002.jpg
slide_004.jpg
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NIH
NORD
Advocacy.jpg
carcinoid2
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Event.jpg
EURORDIS
Rare Disease Day US
Rare Disease Communities

headers

H1

H2

News and Events

News for Patients

News for Patient Organizations

News for Medical Professionals

News for Industry

Latest from Washington

H3

News and Events

News for Patients

News for Patient Organizations

News for Medical Professionals

News for Industry

Latest from Washington

H4

H5

Sections

H6

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slide_001.jpg
slide_005.jpg
slide_003.jpg
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slide_004.jpg
NORD Releases Landmark Study of FDA Orphan Drug Approvals
Read the press release >
Ready the study >
1st Annual US Conference on Rare Diseases and Orphan Products
Read More >
Rao To Serve as OOPD Acting Director
More >
More news >
Help NORD Support New Caucus
More >
Next PNH Meeting to be in Los Angeles on October 15
Information >
Thank You for Supporting Rare Disease Day 2011
Learn more >
More news >
NORD To Host Meeting for Members in New York
More >
The National Foundation for Ectodermal Dysplasias (NFED) Announces New ED
Read More >
More news >
med-rfp
FDA/ DIA Designation Workshops Planned for VA and London
More >
Pediatric Device Grant Awards Announced
Read about 2011/2012 recipients >
More news >
NORD Comments on PDUFA Draft
View statement here>
New Program to Help Start-ups License NIH Biomedical Patents
More >
Message To Congress: Give FDA Funds It Needs
Read More
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Find a patient organization >
Get help with medication costs >
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Facebook
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13 New Compassionate Allowances!
Read the press release >
Appealing Insurance Denials Often A Good Course
More >
The PMP Research Foundation responds to NY Times Article
Details >
FDA Seeks Nominations for Advisory Committees
More >
Congenital Cyanotic Heart Disease (CCHD) Recommended for Uniform Newborn Screening Panel
More >
NIH Seeks Public Common Fund Input
More >
>
Commissioner in WSJ: FDA Remains Gold Standard
Read More >
EURORDIS
Rare Disease Day US
Rare Disease Communities