Alportsyndrome.org - SEO Checker

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Visión general del análisis SEO
Metadatos
100% 
Calidad de la página
61% 
Estructura
87% 
Enlazado
23% 
Servidor
80% 
Factores externos
100% 
Puntuación SEO
Tiempo de carga
1,33 s
Tamaño HTML
637,20 kB
Palabras
746
Medios
30
Cantidad de enlaces
133 internos / 57 externos

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Metadatos

Título
(Extremadamente importante)
Alport Syndrome Foundation - Hope, Action, Support
La longitud del título es óptima (473 píxeles de una longitud máxima de 580 píxeles).
No se repite ninguna palabra en el título.
Meta descripción
(Extremadamente importante)
Alport Syndrome Foundation is a patient-led non-profit dedicated to improving the lives of those affected by Alport Syndrome.
La longitud de la meta descripción es óptima (769 píxeles de una longitud máxima de 1000 píxeles).
Rastreabilidad
(Extremadamente importante)
No se detectan problemas para acceder al sitio web.
Redirección canónica
(Importante)
https://alportsyndrome.org/
La página tiene una redirección canónica correcta.
Idioma
(Poco importante)
Idioma reconocido automáticamente en el contenido: en
Idioma declarado en el código HTML: en-us
Ubicación geográfica del servidor: Estados Unidos de América
El idioma ha sido correctamente declarado en el código HTML: en-us.
Enlaces Alternate/Hreflang
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Otras Metaetiquetas
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No se detecta ninguna metaetiqueta de paginación rel prev en la página.
Dominio
(Poco importante)
El dominio no es un subdominio.
La longitud del nombre del dominio es buena.
El dominio no contiene caracteres especiales.
URL de la página
(Poco importante)
No se detecta ningún parámetro dinámico en la URL.
No se detecta ningún ID de sesión en la URL.
La URL no contiene demasiados subdirectorios.
Codificación de caracteres
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La codificación de caracteres (UTF-8) ha sido declarada correctamente.
Doctype
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La etiqueta doctype HTML 5 está configurada correctamente.
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Favicon
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El favicon está enlazado correctamente.

Metaetiquetas

NombreValor
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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Calidad de la página

Contenido
(Extremadamente importante)
Algunas palabras del título no se repiten en el cuerpo del texto.
El número total de palabras en la página es bueno: 746 palabras.
Un 20% del contenido está constituido por palabras vacías.
La página contiene un listado, lo que indica una buena estructuración del contenido.
Se han encontrado 4 párrafos en esta página.
No se detecta ningún placeholder de texto ni imagen.
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La cantidad media de palabras por frase es buena: 16.33 palabras.
Frames
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Esta página no utiliza ningún frameset.
Optimización para móviles
(Poco importante)
Con 637.2 kB, el documento HTML es demasiado grande.
El valor de la etiqueta viewport es correcto: (width=device-width, initial-scale=1.0, maximum-scale=1.0, user-scalable=0).
Al menos un icono de Apple-Touch ha sido especificado.
Etiquetas Bold y Strong
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El uso de etiquetas de negritas en esta página es óptimo. Te recomendamos emplear hasta 15 etiquetas de negritas en una página.
Optimización de imágenes
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No se detecta ninguna descripción del atributo ALT en 18 imágenes. El contenido de los atributos ALT también es evaluado como texto por los buscadores y es muy importante para la búsqueda de imágenes.
Redes Sociales
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Etiquetas markup adicionales
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HTTPS
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El sitio utiliza HTTPS para transferir datos de forma segura.
Todos los archivos incluidos se transfieren a través de HTTPS.

Lista de medios

URLAtributo ALTTítulo
...s/2019/08/Alport-Syndrome-Foundation.pngAlport Syndrome Foundation
...025/01/AlportConnect-Chicago-2025f-1.pngCarece de atributo ALT
...t/uploads/2024/09/Patient-Registry-1.pngCarece de atributo ALT
/wp-content/uploads/2025/01/logo-UoM.pngCarece de atributo ALT
/wp-content/uploads/2025/01/logo2.pngCarece de atributo ALT
...tent/uploads/2025/01/rdd-logo-footer.pngCarece de atributo ALT
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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
data:[...] Base64Carece de atributo ALT
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Estructura de la página

Encabezado H1
(Extremadamente importante)
New HP
El encabezado H1 es demasiado corto (6 caracteres). Debería tener al menos 20 caracteres.
Encabezados
(Importante)
Algunos encabezados H están vacíos.

Estructura de los encabezados

Jerarquía de encabezadosContenido
H1 New HP
H2 Encabezado vacío
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
Algunos textos ancla se repiten más de una vez en varios enlaces.
Hay 2 links con un texto ancla que no es suficientemente relevante.
La cantidad de enlaces internos es adecuada.
Ningún texto ancla es excesivamente largo.
Ningún enlace interno contiene parámetros dinámicos.
Hay demasiados enlaces externos (57) en esta página.

Enlaces detectados en esta página

EnlacePropiedadesTexto ancla
/for-patients/alport-syndrome-...Podcast
/for-patients/alport-syndrome-...Texto duplicado Podcast
https://www.facebook.com/pages...Nueva ventana Externo Subdominio Facebook
https://www.youtube.com/@Alpor...Nueva ventana Externo Subdominio Youtube
https://www.linkedin.com/compa...Nueva ventana Externo Subdominio Linkedind
https://twitter.com/AlportSynd...Nueva ventana Externo Twitter
https://instagram.com/alportsy...Nueva ventana Externo Instagram
https://www.flickr.com/photos/...Nueva ventana Externo Subdominio Flickr
https://www.bonfire.com/store/...Nueva ventana Externo Subdominio ASF Merch
/registration/FREE MEMBERSHIP
https://alportsyndrome.kindful...Externo Subdominio DONATE NOW
/join-our-efforts/volunteer/VOLUNTEER
https://wordpress-752979-46153...Externo Subdominio Texto duplicado Podcast
/for-patients/alport-syndrome-...Texto duplicado Podcast
https://www.facebook.com/pages...Nueva ventana Externo Subdominio Texto duplicado Facebook
https://www.youtube.com/user/T...Nueva ventana Externo Subdominio Texto duplicado Youtube
https://www.linkedin.com/compa...Nueva ventana Externo Subdominio Linkedin
https://twitter.com/AlportSynd...Nueva ventana Externo Texto duplicado Twitter
https://instagram.com/alportsy...Nueva ventana Externo Texto duplicado Instagram
https://www.flickr.com/photos/...Nueva ventana Externo Subdominio Texto duplicado Flickr
https://www.bonfire.com/store/...Nueva ventana Externo Subdominio Texto duplicado ASF Merch
https://alportsyndrome.org/IMG-ALT Alport Syndrome Foundation
/registration/Texto duplicado FREE MEMBERSHIP
https://alportsyndrome.kindful...Externo Subdominio Texto duplicado DONATE NOW
/join-our-efforts/volunteer/Texto duplicado 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...Nueva ventana Externo Subdominio 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/Texto duplicado 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/Texto duplicado Patient Registry
/for-patients/neptune-natural-...Texto duplicado NEPTUNE (Natural History Study)
/for-patients/clinical-trials/...Active Clinical Trials
/our-foundation/scientific-adv...Scientific Advisory Research Network
/about-alport-syndrome/article...Texto duplicado 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/Texto ancla no relevante
READ MORE
/join-the-asf-alport-patient-r...Texto duplicado Texto ancla no relevante
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...Externo Subdominio VIEW ALL VIDEOS
https://www.instagram.com/alpo...Nueva ventana Externo Subdominio @alportsyndromefndn
https://www.instagram.com/p/DE...Nueva ventana Nofollow Externo Subdominio 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...Nueva ventana Nofollow Externo Subdominio 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...Nueva ventana Nofollow Externo Subdominio 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...Nueva ventana Nofollow Externo Subdominio 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...Nueva ventana Nofollow Externo Subdominio 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...Nueva ventana Nofollow Externo Subdominio 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...Nueva ventana Nofollow Externo Subdominio 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...Nueva ventana Nofollow Externo Subdominio 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...
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/aboutourpatientregistry/Nueva ventana Join the ASF Alport Patient Registry to Support Research.
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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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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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