Alportsyndrome.org - SEO Checker

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Overview of the SEO Check
Meta information
100% 
Page quality
61% 
Page structure
87% 
Link structure
23% 
Server
80% 
External factors
100% 
SEO Score
Response time
1.33 s
File size
637.20 kB
Words
746
Media files
30
Number of links
133 internal / 57 external

Task list of SEO Improvements

Meta specifications

Title
(Critically important)
Alport Syndrome Foundation - Hope, Action, Support
The length of the page title is perfect. (473 pixels out of 580 max pixel length)
There are no duplicate words in the title
Meta description
(Critically important)
Alport Syndrome Foundation is a patient-led non-profit dedicated to improving the lives of those affected by Alport Syndrome.
The length of the meta description is perfect. (769 pixels out of 1000 max pixel length)
Crawlability
(Critically important)
There are no problems in accessing the website.
Canonical URL
(Important)
https://alportsyndrome.org/
There is a valid canonical link specified.
Language
(Somewhat important)
Language detected in text: en
Language defined in HTML: en-us
Server location: United States of America
The following language is defined by HTML: en-us
Alternate/Hreflang Links
(Somewhat important)
There are no alternate links specified on this page.
Other meta tags
(Somewhat important)
There is no rel next meta tag on this page.
There is no rel prev meta tag on this page.
Domain
(Somewhat important)
The domain is no subdomain.
The domain length is good.
The domain does not contain non-latin characters.
Page URL
(Somewhat important)
No parameters were found in the URL.
No session ID was found in the URL.
The URL does not have too many subdirectories.
Charset encoding
(Somewhat important)
The charset encoding (UTF-8) is set correctly.
Doctype
(Nice to have)
The doctype HTML 5 is set correctly.
The doctype is placed at first in the HTML code.
Favicon
(Nice to have)
The favicon is linked correctly.

Meta tags

NameValue
robotsindex, follow, max-image-preview:large, max-snippet:-1, max-video-preview:-1
descriptionAlport Syndrome Foundation is a patient-led non-profit dedicated to improving the lives of those affected by Alport Syndrome.
generatorWP Rocket 3.18
viewportwidth=device-width, initial-scale=1.0, maximum-scale=1.0, user-scalable=0
msapplication-TileImagehttps://alportsyndrome.org/wp-content/uploads/2019/07/favicon.png
article:modified_time2025-02-03T16:30:18+00:00
langen-us
twitter:cardsummary_large_image
og:localeen_US
og:typewebsite
og:titleAlport Syndrome Foundation - Hope, Action, Support
og:descriptionAlport Syndrome Foundation is a patient-led non-profit dedicated to improving the lives of those affected by Alport Syndrome.
og:urlhttps://alportsyndrome.org/
og:site_nameAlport Syndrome Foundation
X-UA-CompatibleIE=edge
charsetUTF-8

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Page quality

Content
(Critically important)
Some words from the page title are not used within the pages content
This page contains 746 words. That's ok.
20% of the text are stop words.
The page contains a listing, which indicates a good text layout.
4 paragraphs were found on this page.
No placeholders texts or images were found.
There are no duplicates on the site.
The average number of words per sentence of 16.33 words is good.
Frames
(Critically important)
This page does not use a frameset.
Mobile optimization
(Somewhat important)
The file size of the HTML document is very large (637.2 kB).
A viewport "width=device-width, initial-scale=1.0, maximum-scale=1.0, user-scalable=0" is provided.
At least one Apple touch icon is specified.
Bold and strong tags
(Somewhat important)
The usage of strong and bold tags is perfect. We recommend the use of up to 15 tags for this page.
Image SEO
(Somewhat important)
18 images have no alt attribute. The content of alt attributes is used by search engines.
Social Networks
(Nice to have)
There are only a few social sharing widgets on the page. Make your website popular in social networks with social sharing widgets.
Additional markup
(Nice to have)
No additional page markup was found.
HTTPS
(Somewhat important)
This website uses HTTPS to protect privacy and integrity of the exchanged data.
All included files are also transferred via HTTPS.

Media list

URLAlt attributeTitle
...s/2019/08/Alport-Syndrome-Foundation.pngAlport Syndrome Foundation
...025/01/AlportConnect-Chicago-2025f-1.pngNo alt attribute provided
...t/uploads/2024/09/Patient-Registry-1.pngNo alt attribute provided
/wp-content/uploads/2025/01/logo-UoM.pngNo alt attribute provided
/wp-content/uploads/2025/01/logo2.pngNo alt attribute provided
...tent/uploads/2025/01/rdd-logo-footer.pngNo alt attribute provided
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data:[...] Base64ASF is pleased to announce the addition of four new members to the Emerging Leadership Council (ELC); Ben Rosengart, Brett Raisman, Mack Bonebrake, and Rachel Denham. All of these members have been significantly impacted by #Alportsyndrome and seek to use their unique skillsets to serve the community. As part of the ELC, they will help create patient resources, promote advocacy and awareness, support others in the community, and more! The ELC was established in 2020 to ensure the voice of those in the 20-30 age range is well-represented in the foundation’s decision-making. Patients in their 20s and 30s are encouraged to contact the ELC to share their stories, learn about relevant ASF resources, and become further engaged within the Alport community. To contact the ELC, please email info@alportsyndrome.org!
data:[...] Base64Way to go, Dan! Congrats for running the Marine Corps Marathon and raising $50,000 for Alport Syndrome Foundation! Together with other families like yours, we’re working to change the stories and outcomes for individuals living with Alport syndrome. We appreciate your dedication. For more information about our rare kidney disease and our Annual Campaign, visit our website (link in bio)!
data:[...] Base64The Paul Silver Enrichment Award cycle ends October 25th! Don’t forget to apply! Swipe to see the 2023 Award Recipients!
data:[...] Base64Learn more about the 2024 Paul Silver Enrichment Award, open to U.S. Alport patients ages 18-24, at the link in our bio! Applications are due October 25th. ”Hi, everyone, my name is Rachel. And I am a recipient of the 2023 Paul Silver Enrichment Award, and I was 23 years old when I applied. I applied because I was also in the midst at the time of applying to graduate programs in genetic counseling, and I knew that this would be a great resource for me to have as I knew I’d have upcoming tuition payments once I started a graduate program. So that’s what I’ve done with the funds so far, and it has been great for me to use those to pay for the first semester’s tuition so that I can focus more so on what I need to be figuring out before I start school and all the studying I need to be doing, that I can focus more on those types of things.”
data:[...] Base64Drs. Simon and Carter of ASF’s Medical Advisory Committee discuss standard of care at #AlportConnectDenver!
data:[...] Base64We are ONE WEEK away from #AlportConnectDenver at the Gaylord Rockies Resort & Convention Center! Due to some last-minute cancellations, extremely limited tickets remain and event registration will close tomorrow, Monday, July 22nd. See link in bio for ticket details. We are excited to bring together patients/families from across the country with medical professionals who have expertise in our rare disease and researchers! All event registrants will receive an email communication early this week with critical event details. After months of planning, we are thrilled to host a memorable weekend and are excited to see new and returning faces! 💜🏔️
data:[...] Base64In honor of #WorldKidneyDay and #AlportAwareness Month, ASF is grateful to share a personal message to our community from @alyraisman, champion gymnast and kidney health advocate: 𝘈𝘭𝘱𝘰𝘳𝘵 𝘴𝘺𝘯𝘥𝘳𝘰𝘮𝘦 𝘩𝘢𝘴 𝘢𝘧𝘧𝘦𝘤𝘵𝘦𝘥 𝘮𝘺 𝘧𝘢𝘮𝘪𝘭𝘺 𝘧𝘰𝘳 𝘮𝘶𝘭𝘵𝘪𝘱𝘭𝘦 𝘨𝘦𝘯𝘦𝘳𝘢𝘵𝘪𝘰𝘯𝘴 𝘢𝘯𝘥 𝘐’𝘮 𝘱𝘢𝘴𝘴𝘪𝘰𝘯𝘢𝘵𝘦 𝘢𝘣𝘰𝘶𝘵 𝘳𝘢𝘪𝘴𝘪𝘯𝘨 𝘮𝘰𝘳𝘦 𝘢𝘸𝘢𝘳𝘦𝘯𝘦𝘴𝘴 𝘧𝘰𝘳 𝘣𝘦𝘵𝘵𝘦𝘳 𝘵𝘳𝘦𝘢𝘵𝘮𝘦𝘯𝘵 𝘰𝘱𝘵𝘪𝘰𝘯𝘴. 𝘛𝘩𝘳𝘰𝘶𝘨𝘩 𝘰𝘶𝘳 𝘰𝘸𝘯 𝘦𝘹𝘱𝘦𝘳𝘪𝘦𝘯𝘤𝘦𝘴, 𝘮𝘺 𝘧𝘢𝘮𝘪𝘭𝘺 𝘩𝘢𝘴 𝘭𝘦𝘢𝘳𝘯𝘦𝘥 𝘵𝘩𝘦 𝘪𝘮𝘱𝘰𝘳𝘵𝘢𝘯𝘤𝘦 𝘰𝘧 𝘱𝘢𝘵𝘪𝘦𝘯𝘵𝘴’ 𝘬𝘯𝘰𝘸𝘭𝘦𝘥𝘨𝘦 𝘢𝘯𝘥 𝘶𝘯𝘥𝘦𝘳𝘴𝘵𝘢𝘯𝘥𝘪𝘯𝘨 𝘰𝘧 𝘵𝘩𝘪𝘴 𝘥𝘪𝘴𝘦𝘢𝘴𝘦. 𝘐 𝘣𝘦𝘭𝘪𝘦𝘷𝘦 𝘪𝘵’𝘴 𝘦𝘴𝘴𝘦𝘯𝘵𝘪𝘢𝘭 𝘧𝘰𝘳 𝘱𝘢𝘵𝘪𝘦𝘯𝘵𝘴 𝘵𝘰 𝘧𝘦𝘦𝘭 𝘦𝘮𝘱𝘰𝘸𝘦𝘳𝘦𝘥 𝘵𝘰 𝘴𝘱𝘦𝘢𝘬 𝘶𝘱 𝘢𝘯𝘥 𝘢𝘴𝘬 𝘲𝘶𝘦𝘴𝘵𝘪𝘰𝘯𝘴 𝘵𝘰 𝘭𝘦𝘢𝘳𝘯 𝘮𝘰𝘳𝘦. 𝘈𝘚𝘍 𝘩𝘢𝘴 𝘴𝘩𝘢𝘳𝘦𝘥 𝘸𝘪𝘵𝘩 𝘶𝘴 𝘵𝘩𝘢𝘵 𝘸𝘦 𝘦𝘢𝘤𝘩 𝘩𝘢𝘷𝘦 𝘶𝘯𝘪𝘲𝘶𝘦 𝘨𝘦𝘯𝘦𝘵𝘪𝘤 𝘱𝘳𝘰𝘧𝘪𝘭𝘦𝘴 𝘪𝘯𝘧𝘭𝘶𝘦𝘯𝘤𝘪𝘯𝘨 𝘵𝘩𝘦 𝘱𝘳𝘰𝘨𝘳𝘦𝘴𝘴𝘪𝘰𝘯 𝘰𝘧 𝘰𝘶𝘳 𝘴𝘺𝘮𝘱𝘵𝘰𝘮𝘴 𝘢𝘯𝘥 𝘨𝘦𝘯𝘦𝘵𝘪𝘤 𝘵𝘦𝘴𝘵𝘪𝘯𝘨 𝘢𝘯𝘥 𝘦𝘥𝘶𝘤𝘢𝘵𝘪𝘰𝘯 𝘢𝘳𝘦 𝘤𝘳𝘶𝘤𝘪𝘢𝘭 𝘵𝘰𝘰𝘭𝘴 𝘧𝘰𝘳 𝘥𝘰𝘤𝘵𝘰𝘳𝘴 𝘵𝘰 𝘣𝘦𝘴𝘵 𝘵𝘳𝘦𝘢𝘵 𝘈𝘭𝘱𝘰𝘳𝘵 𝘱𝘢𝘵𝘪𝘦𝘯𝘵𝘴. 𝘐’𝘮 𝘴𝘰 𝘨𝘳𝘢𝘵𝘦𝘧𝘶𝘭 𝘧𝘰𝘳 𝘈𝘚𝘍’𝘴 𝘦𝘧𝘧𝘰𝘳𝘵𝘴 𝘪𝘯 𝘢𝘥𝘷𝘢𝘯𝘤𝘪𝘯𝘨 𝘯𝘦𝘸 𝘳𝘦𝘴𝘦𝘢𝘳𝘤𝘩, 𝘦𝘥𝘶𝘤𝘢𝘵𝘪𝘰𝘯, 𝘢𝘯𝘥 𝘴𝘶𝘱𝘱𝘰𝘳𝘵𝘪𝘯𝘨 𝘵𝘩𝘪𝘴 𝘤𝘰𝘮𝘮𝘶𝘯𝘪𝘵𝘺. 𝘞𝘰𝘳𝘬𝘪𝘯𝘨 𝘵𝘰𝘨𝘦𝘵𝘩𝘦𝘳 𝘵𝘰 𝘩𝘦𝘭𝘱 𝘵𝘩𝘦𝘴𝘦 𝘦𝘧𝘧𝘰𝘳𝘵𝘴 𝘸𝘪𝘭𝘭 𝘩𝘰𝘱𝘦𝘧𝘶𝘭𝘭𝘺 𝘩𝘦𝘭𝘱 𝘪𝘮𝘱𝘳𝘰𝘷𝘦 𝘢𝘯𝘥 𝘴𝘢𝘷𝘦 𝘵𝘩𝘦 𝘭𝘪𝘷𝘦𝘴 𝘰𝘧 𝘱𝘢𝘵𝘪𝘦𝘯𝘵𝘴, 𝘧𝘳𝘪𝘦𝘯𝘥𝘴, 𝘢𝘯𝘥 𝘧𝘢𝘮𝘪𝘭𝘪𝘦𝘴 𝘪𝘮𝘱𝘢𝘤𝘵𝘦𝘥 𝘣𝘺 𝘈𝘭𝘱𝘰𝘳𝘵 𝘴𝘺𝘯𝘥𝘳𝘰𝘮𝘦. #Alportsyndrome
data:[...] Base64As a #raredisease, #Alportsyndrome is commonly misdiagnosed. Genetic testing is a powerful tool for accurate diagnosis, which can unlock access to treatments, clinical trial opportunities, and ways to connect with the larger community of patients and families. For more information, visit alportsyndrome.org. #RareDiseaseDay
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Page structure

H1 heading
(Critically important)
New HP
The H1 heading is too short (6 characters). It should be at least 20 Characters long.
Headings
(Important)
Some headings do not have any content.

Heading structure

Heading levelContent
H1 New HP
H2 Empty heading
H2 Follow @alportsyndromefndn
H2 Join the ASF Alport Patient Registry to Support Research.
H3 January 2025 Newsletter
H3 JOIN THE ASF ALPORT PATIENT REGISTRY
H3 THERE IS GREAT REASON TO BE HOPEFUL ABOUT YOUR FUTURE!
H3 “We’re in your corner!”
H3 Learn
H3 Engage
H3 Donate
H4 ASF Alport Patient Registry: Help Advance Alport Research!
H4 Alport Connect 2023 Highlights Video
H4 Alport Connect 2023 Keynote Address: Hopeful Advances in Research
H4 Living Kidney Donor Interview: Mack
H4 Alport Syndrome Female Diagnosis Stories
Some anchor texts are used more than once.
There are 2 links with a trivial anchor text.
The number of internal links is ok.
None of the anchor texts is too long.
All internal links are not using dynamic parameters.
There are too many external links (57) on this page.

Found links on this page

LinkAttributesAnchor text
/for-patients/alport-syndrome-...Podcast
/for-patients/alport-syndrome-...Text duplicate Podcast
https://www.facebook.com/pages...New window External Subdomain Facebook
https://www.youtube.com/@Alpor...New window External Subdomain Youtube
https://www.linkedin.com/compa...New window External Subdomain Linkedind
https://twitter.com/AlportSynd...New window External Twitter
https://instagram.com/alportsy...New window External Instagram
https://www.flickr.com/photos/...New window External Subdomain Flickr
https://www.bonfire.com/store/...New window External Subdomain ASF Merch
/registration/FREE MEMBERSHIP
https://alportsyndrome.kindful...External Subdomain DONATE NOW
/join-our-efforts/volunteer/VOLUNTEER
https://wordpress-752979-46153...External Subdomain Text duplicate Podcast
/for-patients/alport-syndrome-...Text duplicate Podcast
https://www.facebook.com/pages...New window External Subdomain Text duplicate Facebook
https://www.youtube.com/user/T...New window External Subdomain Text duplicate Youtube
https://www.linkedin.com/compa...New window External Subdomain Linkedin
https://twitter.com/AlportSynd...New window External Text duplicate Twitter
https://instagram.com/alportsy...New window External Text duplicate Instagram
https://www.flickr.com/photos/...New window External Subdomain Text duplicate Flickr
https://www.bonfire.com/store/...New window External Subdomain Text duplicate ASF Merch
https://alportsyndrome.org/IMG-ALT Alport Syndrome Foundation
/registration/Text duplicate FREE MEMBERSHIP
https://alportsyndrome.kindful...External Subdomain Text duplicate DONATE NOW
/join-our-efforts/volunteer/Text duplicate VOLUNTEER
/our-foundation/who-we-are/About ASF
/about-alport-syndrome/About Alport Syndrome
/about-alport-syndrome/What is Alport syndrome
/about-alport-syndrome/voice-o...Voice of the Patient Report (FDA)
/about-alport-syndrome/diagnosis/Diagnosis
/treatment/Treatment
/about-alport-syndrome/hearing...Hearing Loss Overview
/treatment/medication-monitoring/Medications & Monitoring
/eye-abnormalities/Eye Abnormalities and Research
/about-alport-syndrome/top-5-i...Top 5 Tips for Women
/about-alport-syndrome/top-5-i...Top 5 Tips for Teens
/about-alport-syndrome/top-5-i...Top 5 Tips for Young Adults
/about-alport-syndrome/top-5-i...Top 5 Tips for Adults / Caregivers
/about-alport-syndrome/article...Published Articles and Papers
/for-patients/top-5-things-to-...Patients
/our-foundation/letter-from-th...Letter from Exec. Director
/for-patients/top-5-things-to-...Top 5 Things to Know Right Now
https://www.youtube.com/@Alpor...New window External Subdomain Educational Videos
/for-patients/patient-resources/Patient Resources
/about-alport-syndrome/resourc...Resources for Parents and Caregivers
/treatment/dialysis-overview/Dialysis Overview
/treatment/transplant/Transplant
/aboutourpatientregistry/Patient Registry
/for-patients/neptune-natural-...NEPTUNE (Natural History Study)
/for-patients/clinical-trials/...Clinical Trials – Active Studies
/direct-connect-meetings/Direct Connect Meetings
/for-patients/alport-connect/Alport Connect Meetings
/join-our-efforts/volunteer/Volunteer
/for-patients/renal-diet-and-n...Renal Diet & Nutrition
/for-patients/mental-health-re...Mental Health Resources
/for-patients/podcasts/Podcast Appearances
/resources-for-medical-profess...Medical Professionals
/resources-for-medical-profess...Resources for Medical Professionals
/about-alport-syndrome/top-5-t...Top 5 for Medical Professionals
/patient-guide-by-patients-for...Patient Guide
/aboutourpatientregistry/Text duplicate Patient Registry
/our-foundation/medical-adviso...Medical Advisory Committee
/asf-research-funding-program-...Research & Pharma
/asf-research-funding-program-...ASF Research Program
/asf-research-program-impact/Impact
/about-alport-syndrome/top-5-t...For Researchers and Pharma Industry
/aboutourpatientregistry/Text duplicate Patient Registry
/for-patients/neptune-natural-...Text duplicate NEPTUNE (Natural History Study)
/for-patients/clinical-trials/...Active Clinical Trials
/our-foundation/scientific-adv...Scientific Advisory Research Network
/about-alport-syndrome/article...Text duplicate Published Articles and Papers
/for-patients/top-5-things-to-...Patient Education
/for-patients/research-opportu...Patient Research Opportunities
A-TITLE Research Opportunities
/for-patients/clinical-trials/...Clinical Trials
/january-2025-newsletter/Trivial anchor text
READ MORE
/join-the-asf-alport-patient-r...Text duplicate Trivial anchor text
READ MORE
/events/2025-alport-research-h...Feb 10 2025 Alport Research Hub Meeting
/events/2025-ipna-congress/Feb 19 - Feb 23 IPNA 2025 – 20th Congress of the International Pediatric Nephrology Association
/events/rare-disease-day-2025/Feb 28 Rare Disease Day 2025
/our-foundation/who-we-are/LEARN ABOUT ALPORT SYNDROME FOUNDATION
https://www.youtube.com/@Alpor...External Subdomain VIEW ALL VIDEOS
https://www.instagram.com/alpo...New window External Subdomain @alportsyndromefndn
https://www.instagram.com/p/DE...New window Nofollow External Subdomain ASF is pleased to announce the addition of four ne
IMG-ALT ASF is pleased to announce the addition of four new members to the Emerging Leadership Council (ELC); Ben Rosengart, Brett Raisman, Mack Bonebrake, and Rache...
https://www.instagram.com/p/DB...New window Nofollow External Subdomain Way to go, Dan! Congrats for running the Marine Co
IMG-ALT Way to go, Dan! Congrats for running the Marine Corps Marathon and raising $50,000 for Alport Syndrome Foundation! Together with other families like yours, w...
https://www.instagram.com/p/DA...New window Nofollow External Subdomain The Paul Silver Enrichment Award cycle ends Octobe
IMG-ALT The Paul Silver Enrichment Award cycle ends October 25th! Don’t forget to apply! Swipe to see the 2023 Award Recipients!
https://www.instagram.com/reel...New window Nofollow External Subdomain Learn more about the 2024 Paul Silver Enrichment A
IMG-ALT Learn more about the 2024 Paul Silver Enrichment Award, open to U.S. Alport patients ages 18-24, at the link in our bio! Applications are due October 25th. ”...
https://www.instagram.com/p/C9...New window Nofollow External Subdomain Drs. Simon and Carter of ASF’s Medical Advisory
IMG-ALT Drs. Simon and Carter of ASF’s Medical Advisory Committee discuss standard of care at #AlportConnectDenver!
https://www.instagram.com/p/C9...New window Nofollow External Subdomain We are ONE WEEK away from #AlportConnectDenver at
IMG-ALT We are ONE WEEK away from #AlportConnectDenver at the Gaylord Rockies Resort & Convention Center! Due to some last-minute cancellations, extremely limited ti...
https://www.instagram.com/p/C4...New window Nofollow External Subdomain In honor of #WorldKidneyDay and #AlportAwareness M
IMG-ALT In honor of #WorldKidneyDay and #AlportAwareness Month, ASF is grateful to share a personal message to our community from @alyraisman, champion gymnast and k...
https://www.instagram.com/p/C3...New window Nofollow External Subdomain As a #raredisease, #Alportsyndrome is commonly mis
IMG-ALT As a #raredisease, #Alportsyndrome is commonly misdiagnosed. Genetic testing is a powerful tool for accurate diagnosis, which can unlock access to treatments...
https://www.instagram.com/alpo...New window Nofollow External Subdomain Follow on Instagram
/aboutourpatientregistry/New window Join the ASF Alport Patient Registry to Support Research.
/aboutourpatientregistry/Learn More
https://alportsyndrome.org/No Text
/cdn-cgi/l/email-protection[email protected]
/about-alport-syndrome/Text duplicate About Alport Syndrome
/for-patients/top-5-things-to-...Text duplicate Top 5 Things to Know Right Now
/our-foundation/who-we-are/Our Foundation
/asf-research-funding-program-...Subdomain Text duplicate ASF Research Program
/for-patients/clinical-trials/Text duplicate Clinical Trials
/aboutourpatientregistry/Text duplicate Patient Registry
/for-patients/neptune-natural-...Text duplicate NEPTUNE (Natural History Study)
/join-our-efforts/volunteer/Volunteer Opportunities
/direct-connect-meetings/Text duplicate Direct Connect Meetings
https://www.facebook.com/group...External Subdomain Facebook Support Group
/join-our-efforts/advocacy/Advocacy
https://alportsyndrome.kindful...External Subdomain Donate Now
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alportsyndrome.org
Alport Syndrome Foundation - Hope, Action, Support
Alport Syndrome Foundation is a patient-led non-profit dedicated to improving the lives of those affected by Alport Syndrome.

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Syndrome81%Check
Alport Syndrome79%Check
Alport77%Check
Syndrome Foundation73%Check
ALPORT SYNDROME FOUNDATION72%Check
FOUNDATION61%Check
Alport Connect61%Check
ASF ALPORT PATIENT60%Check
ALPORT PATIENT REGISTRY60%Check
Alport Research60%Check
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