• Patients & Caregivers
  • Patient Organizations
  • For Clinicians & Researchers
  • NORD En español
  • Contact Us
NORD logo with tag for website.
  • Donate
  • Rare Disease News
  • Find a Rare Disease
  • About Us
  • Events
  • Understanding Rare Disease
        • Where to start
          • Rare Disease Facts and Statistics
          • NORD’s Rare Disease Database
          • Rare Disease Video Library
          • Help for People with Undiagnosed Medical Conditions
          • Find A Rare Disease Organization
          • Diagnóstico Raro en Niños: Una Guía para los Padres para Encontrar el Diagnóstico de una Enfermedad Rara
          • A PCP Primer to Diagnosing Rare Disease in Children
        • Stay informed
          • Stories That Inspire
          • RareEdu® – Online Learning Platform
          • Rare Disease Day®
          • Resource Library
          • State Resource Center
          • Publications On Rare Disease
        • Featured NORD Event
          • LRLS Thumbnail for rarediseases.orgNORD® Living Rare, Living Stronger® Patient & Family Meeting
          • Learn More
  • Living with a Rare Disease
        • Manage your care
          • Getting Help & Support
          • Managing Your Disease
          • Telemedicina – Para Pacientes y Cuidadores
        • We can help
          • How NORD Can Help
          • Speak To Someone at NORD
          • Rare Disease Centers Of Excellence
          • Patient Assistance Programs
          • Explore Clinical Trials
          • Find A Patient Organization
          • Caregiver Resources
        • Discover Local Resources
        • State-Resource-Cente
  • Community Support
      • Where to start
        • Rare Diseases Defined
        • Financial & Medical Assistance
        • Call Center & Information Services
        • Bringing Together Your Community
      • Mentoring organizations
        • NORD Member List
        • Start a Rare Disease Organization
        • Membership Program
        • Becoming Research Ready
        • Patient-Focused Drug Development
      • Improving clinical care
        • NORD Claim Your Care®
        • Rare Disease Centers of Excellence
        • Continuing Medical Education (CME)
      • Partnering with the community
        • Corporate Council
        • National Partnerships
        • Global Partnerships
        • Rare Cancer Coalition
        • NORD Rare Impact Awards®
      • Featured NORD Event
        • LRLS Thumbnail for rarediseases.orgNORD® Living Rare, Living Stronger® Patient & Family Meeting
        • Learn More
  • Advancing Research
      • For patients
        • List of Rare Diseases
        • Gene Therapy for Rare Disease
        • Find Clinical Trials & Research Studies
      • For researchers
        • Request for Proposals
        • Research Grant Programs
        • Data Standards for Rare Diseases
        • Patient-Focused Drug Development Meetings
      • For clinicians
        • Resources for Patients
        • Find a Rare Disease Care Center
        • Continuing Medical Education (CME)
      • Connect
        • IAMRARE® Program Powered by NORD
        • Rare Disease Cures Accelerator (RDCA-DAP)
        • All of Us Study
      • Featured NORD Event
        • Symposium thumbnailNORD Rare Disease Scientific Symposium
        • Learn More
  • Driving Policy
        • NORD policy and you
          • Public Policy Positions
          • Policy Statements & Letters to Policymakers
          • Rare Disease Advisory Councils
          • NORD State Report Card®
        • Taking action
          • Join the Rare Action Network®
          • Take Action
          • Advocate for Rare Disease Policies as a Health Care Professional
        • Join A Current Campaign.
          • NORD policy alert notification icon imageLearn about our current
            policy goals
          • Take Action
        • Featured NORD Event
        • Summit thumbnailNORD® Rare Diseases & Orphan Products Breakthrough Summit®
        • Learn More
  • Get Involved
      • Raising Awareness & Funds with NORD
        • Do-It-Yourself NORD Fundraiser
        • NORD Students for Rare®
        • Sports & Fitness Fundraisers
        • Media Inquiries
      • In your community
        • Attend An Upcoming Event
        • Find a Rare Disease Patient Organization
        • Stay Informed With NORD’s Email Newsletter
        • Rare Disease Day®
      • Patient stories
        • Share Your Story
        • Careers At NORD
        • Intern At NORD
        • Jobs At Patient Disease Organizations
      • Corporate Council
        • Corporate Council
        • Corporate Council Members
        • Join Corporate Council
        • Corporate Council – Code of Conduct
      • Show Your Support
        • Donate to NORD
        • Volunteer Application
        • Store
  • Donate
  • Understanding Rare Disease
    • Where to start
      • Rare Disease Facts and Statistics
      • NORD’s Rare Disease Database
      • Rare Disease Video Library
      • What It Means To Be Undiagnosed
      • Find A Rare Disease Organization
      • Diagnóstico Raro en Niños: Una Guía para los Padres para Encontrar el Diagnóstico de una Enfermedad Rara
      • A PCP Primer to Diagnosing Rare Disease in Children
    • Stay informed
      • Stories That Inspire
      • RareEdu® – Online Learning Platform
      • Rare Disease Day
      • Resource Library
      • State Resource Center – Find Local Resources
      • Publications On Rare Disease
    • NORD® Living Rare, Living Stronger® Patient & Family Meeting
      • Learn More
  • Living with a Rare Disease
    • Manage your care
      • Getting Help & Support
      • Managing Your Disease
    • We can help
      • How NORD Can Help
      • Speak To Someone at NORD
      • Rare Disease Center Of Excellence
      • Patient Assistance Programs
      • Explore Clinical Trials
      • Find A Patient Organization
      • Caregiver Resources
      • State Resource Center – Discover Local Resources
  • Community Support
    • Where to start
      • Rare Diseases Defined
      • Financial & Medical Assistance
      • Call Center & Information Services
      • Bringing Together Your Community
    • Mentoring organizations
      • NORD Member List
      • Start a Rare Disease Organization
      • Membership Program
      • Becoming Research Ready
      • Launching Registries & Natural History Studies
      • Patient-Focused Drug Development
    • Improving clinical care
      • Claim Your Care
      • Rare Disease Centers of Excellence
      • Continuing Medical Education (CME)
    • Partnering with the community
      • Corporate Council
      • National Partnerships
      • Global Parnerships
    • NORD® Living Rare, Living Stronger® Patient & Family Meeting
      • Learn More
  • Advancing Research
    • For patients
      • List of Rare Diseases
      • Gene Therapy for Rare Disease
      • Find Clinical Trials & Research Studies
    • For researchers
      • Request for Proposals
      • Research Grant Programs
      • Data Standards for Rare Diseases
    • For clinicians
      • Resources for Patients
      • Find a Rare Disease Care Center
      • Continuing Medical Education (CME)
    • Connect
      • IAMRARE® Program Powered by NORD
      • Rare Disease Cures Accelerator (RDCA-DAP)
      • All of Us Study
      • Add Your Expertise
    • NORD Rare Disease Scientific Symposium
      • Learn More
  • Driving Policy
    • NORD policy and you
      • Today’s Policy Issues
      • NORD’s Policy Statements
      • Rare Disease Advisory Councils
      • NORD State Report Card
    • Taking action
      • Join the Rare Action Network®
      • Contact your Representative
      • Take Action
      • Advocate for Rare Disease Policies as a Health Care Professional
    • Join A Current Campaign.
      • Learn about our current policy goals
  • Get Involved
    • Raising awareness and funds with NORD
      • Do-It-Yourself NORD Fundraiser
      • NORD Students for Rare
      • Sports & Fitness Fundraisers
      • Media Inquiries
    • In your community
      • Attend An Upcoming Event
      • Find a Rare Disease Patient Organization
      • Stay Informed With NORD’s Email Newsletter
      • Rare Disease Day®
    • Patient stories
      • Share Your Story
      • Careers At NORD
      • Intern At NORD
      • Jobs At Patient Disease Organizations
    • Show your support
      • Donate
      • Volunteer Application
      • Visit the NORD Store
  • Rare Disease News
  • Resource Library
  • About Us
  • For Clinicians & Researchers
  • For Patient Organizations
Home / Patient Organizations / Patient Organizations
Ronald McDonald House Charities
Teléfono: 630-623-7048 Correo electrónico: [email protected] Fax: 630-623-7488
https://rarediseases.org/es/organizations/ronald-mcdonald-house-charities/
Ver perfil >
Rose Kushner ‘s Women’s Breast Cancer Advisory Center
Correo electrónico: [email protected]
Enfermedades raras relacionadas: Paget’s Disease of the Breast
https://rarediseases.org/es/organizations/rose-kushner-s-womens-breast-cancer-advisory-center/
Ver perfil >
Rothberg Institute For Childhood Diseases
Teléfono: 203-458-7100 Correo electrónico: [email protected] Fax: 203-458-2514
Enfermedades raras relacionadas: Esclerosis tuberosa
https://rarediseases.org/es/organizations/rothberg-institute-for-childhood-diseases/
Ver perfil >
Rothmund-Thomson Syndrome (RTS) Foundation
Miembro NORD
Correo electrónico: [email protected]
Enfermedades raras relacionadas: Síndrome de Rothmund-Thomson
https://rarediseases.org/es/organizations/rothmund-thomson-syndrome-rts-foundation/
Ver perfil >
RP Fighting Blindness
Correo electrónico: [email protected]
https://rarediseases.org/es/organizations/rp-fighting-blindness/
Ver perfil >
RTC Portland – Family Support and Children’s Mental Health & Training Center
Teléfono: 503-725-4040 Correo electrónico: [email protected] Fax: 503-725-4180
https://rarediseases.org/es/organizations/rtc-portland-family-support-and-childrens-mental-health-training-center/
Ver perfil >
Rubinstein-Taybi Syndrome, UK Support Group
Correo electrónico: [email protected]
Enfermedades raras relacionadas: Rubinstein-Taybi Syndrome
https://rarediseases.org/es/organizations/rubinstein-taybi-syndrome-uk-support-group/
Ver perfil >
RUNX1 Research Program
Enfermedades raras relacionadas: Trastorno plaquetario familiar con neoplasia mieloide asociada
https://rarediseases.org/es/organizations/runx1-research-program/
Ver perfil >
Rush University Medical Center
Teléfono: 312-942-5000 Correo electrónico: [email protected]
https://rarediseases.org/es/organizations/rush-university-medical-center/
Ver perfil >
SADS UK (Sudden Arrhythmic Death Syndrome)
Teléfono: 127-781-1215 Correo electrónico: [email protected]
Enfermedades raras relacionadas: Síndrome de QT Corto, Síndrome de Andersen-Tawil, Timothy Syndrome, ...
https://rarediseases.org/es/organizations/sads-uk-sudden-arrhythmic-death-syndrome/
Ver perfil >
Sail To Prevail
Teléfono: 401-849-8898 Correo electrónico: [email protected] Fax: 401-849-8898
https://rarediseases.org/es/organizations/sail-to-prevail/
Ver perfil >
Salla Treatment And Research
Enfermedades raras relacionadas: Trastorno de depósito de ácido siálico libre
https://rarediseases.org/es/organizations/salla-treatment-and-research/
Ver perfil >
Sam Day Foundation
Correo electrónico: [email protected]
https://rarediseases.org/es/organizations/sam-day-foundation/
Ver perfil >
SAMHSA’s Center for Substance Abuse Prevention
https://rarediseases.org/es/organizations/samhsas-center-for-substance-abuse-prevention/
Ver perfil >
San Diego Brachial Plexus Network
Teléfono: 866-877-7004 Correo electrónico: [email protected] Fax: 844-221-2821
https://rarediseases.org/es/organizations/san-diego-brachial-plexus-network/
Ver perfil >
San Diego Regional Center for the Developmental Disabilities
Teléfono: 858-576-2996 Correo electrónico: [email protected] Fax: 858-576-2873
https://rarediseases.org/es/organizations/san-diego-regional-center-for-the-developmental-disabilities/
Ver perfil >
SANE Australia
Correo electrónico: [email protected]
https://rarediseases.org/es/organizations/sane-australia/
Ver perfil >
Sanfilippo Children’s Foundation
Correo electrónico: [email protected]
Enfermedades raras relacionadas: Mucopolisacaridosis tipo III
https://rarediseases.org/es/organizations/sanfilippo-childrens-foundation/
Ver perfil >
Sanfilippo Foundation Switzerland
Correo electrónico: [email protected]
Enfermedades raras relacionadas: Mucopolisacaridosis tipo III
https://rarediseases.org/es/organizations/sanfilippo-foundation-switzerland/
Ver perfil >
Sarcoidosis & Lyme Disease Support Australia
Correo electrónico: [email protected]
https://rarediseases.org/es/organizations/sarcoidosis-lyme-disease-support-australia/
Ver perfil >
Sarcoidosis Center
Teléfono: 901-761-5877 Correo electrónico: [email protected] Fax: 901-761-2280
https://rarediseases.org/es/organizations/sarcoidosis-center/
Ver perfil >
Sarcoidosis Online Sites (S.O.S.)
Teléfono: 239-945-2414 Correo electrónico: [email protected]
https://rarediseases.org/es/organizations/sarcoidosis-online-sites-s-o-s/
Ver perfil >
Sarcoma Alliance
Teléfono: 415-381-7236 Correo electrónico: [email protected] Fax: 415-381-7235
Enfermedades raras relacionadas: Sarcoma alveolar de partes blandas, Leiomyosarcoma, Mesenchymal Chondrosarcoma, ...
https://rarediseases.org/es/organizations/sarcoma-alliance/
Ver perfil >
Sarcoma Alliance for Research through Collaboration
Correo electrónico: [email protected]
https://rarediseases.org/es/organizations/sarcoma-alliance-for-research-through-collaboration/
Ver perfil >
Sarcoma Foundation of America
Correo electrónico: [email protected]
Enfermedades raras relacionadas: Sarcoma alveolar de partes blandas, Leiomyosarcoma, Mesenchymal Chondrosarcoma, ...
https://rarediseases.org/es/organizations/sarcoma-foundation-of-america/
Ver perfil >
SATB2 Gene Foundation
Miembro NORD
Teléfono: 678-832-9133 Correo electrónico: [email protected]
https://rarediseases.org/es/organizations/satb2-gene-foundation/
Ver perfil >
Save Babies Through Screening Foundation
Teléfono: 610-251-9876 Correo electrónico: [email protected] Fax: 610-647-5757
Enfermedades raras relacionadas: Short Chain Acyl CoA Dehydrogenase Deficiency, Homocystinuria due to Cystathionine Beta-Synthase Deficiency, Tyrosinemia Type 1, ...
https://rarediseases.org/es/organizations/save-babies-through-screening-foundation/
Ver perfil >
SBS Cure Project
Correo electrónico: [email protected]
Enfermedades raras relacionadas: Síndrome del intestino corto
https://rarediseases.org/es/organizations/sbs-cure-project/
Ver perfil >
SCA27b Ataxia Foundation
Correo electrónico: [email protected]
Enfermedades raras relacionadas: Ataxias espinocerebelosas autosómicas dominantes
https://rarediseases.org/es/organizations/sca27b-ataxia-foundation/
Ver perfil >
Scarring Alopecia Foundation (SAF)
Miembro NORD
Correo electrónico: [email protected]
Enfermedades raras relacionadas: Cicatricial Alopecia
https://rarediseases.org/es/organizations/scarring-alopecia-foundation-saf/
Ver perfil >
Schepens Eye Research Institute
Teléfono: 617-912-0100 Correo electrónico: [email protected] Fax: 617-912-0101
Enfermedades raras relacionadas: Chandler’s Syndrome, Síndrome de Duane, Eales Disease, ...
https://rarediseases.org/es/organizations/schepens-eye-research-institute/
Ver perfil >
Schinzel-Giedion Syndrome Foundation
Correo electrónico: [email protected]
Enfermedades raras relacionadas: Schinzel Giedion Syndrome
https://rarediseases.org/es/organizations/schinzel-giedion-syndrome-foundation/
Ver perfil >
Schiz Kidz Buddies – Schizencephaly Support Group
Correo electrónico: [email protected]
https://rarediseases.org/es/organizations/schiz-kidz-buddies-schizencephaly-support-group/
Ver perfil >
Schizophrenia Society of Canada
Teléfono: 204-786-1616 Correo electrónico: [email protected] Fax: 204-783-4898
https://rarediseases.org/es/organizations/schizophrenia-society-of-canada/
Ver perfil >
SCID Foundation
Correo electrónico: [email protected]
https://rarediseases.org/es/organizations/scid-foundation/
Ver perfil >
Scleroderma and Raynaud’s UK
Correo electrónico: [email protected]
Enfermedades raras relacionadas: Esclerodermia sistémica, Scleroderma
https://rarediseases.org/es/organizations/scleroderma-and-raynauds-uk/
Ver perfil >
Scleroderma Research Foundation
Correo electrónico: [email protected]
https://rarediseases.org/es/organizations/scleroderma-research-foundation/
Ver perfil >
Scleroderma Super Starz FB/Insta Support Group Leader
https://rarediseases.org/es/organizations/scleroderma-super-starz-fb-insta-support-group-leader/
Ver perfil >
Scottish Society for Autism
Teléfono: 125-972-0044 Correo electrónico: [email protected] Fax: 125-972-0051
https://rarediseases.org/es/organizations/scottish-society-for-autism/
Ver perfil >
SDSF
https://rarediseases.org/es/organizations/sdsf/
Ver perfil >
Seattle Children’s Hospital
Teléfono: 206-987-2000 Fax: 206-526-2217
https://rarediseases.org/es/organizations/seattle-childrens-hospital/
Ver perfil >
Second Wind Lung Transplant Association, Inc.
Teléfono: 512-847-9303 Correo electrónico: [email protected]
Enfermedades raras relacionadas: Idiopathic Pulmonary Fibrosis, Eisenmenger Syndrome, Lymphangioleiomyomatosis ...
https://rarediseases.org/es/organizations/second-wind-lung-transplant-association-inc/
Ver perfil >
Selective Mutism Foundation, Inc.
Correo electrónico: [email protected]
https://rarediseases.org/es/organizations/selective-mutism-foundation-inc/
Ver perfil >
Selective Mutism Group
Teléfono: 215-887-5748 Correo electrónico: [email protected]
https://rarediseases.org/es/organizations/selective-mutism-group/
Ver perfil >
Self-Help Information Service of Nebraska
Teléfono: 402-476-9668 Correo electrónico: [email protected] Fax: 402-434-3972
https://rarediseases.org/es/organizations/self-help-information-service-of-nebraska/
Ver perfil >
Selfhelp
Teléfono: 212-836-1865 Correo electrónico: [email protected] Fax: 212-956-1652
https://rarediseases.org/es/organizations/selfhelp/
Ver perfil >
SeriousFun Children’s Network
Teléfono: 203-562-1203 Correo electrónico: [email protected] Fax: 203-341-8707
https://rarediseases.org/es/organizations/seriousfun-childrens-network/
Ver perfil >
SETBP1 Society
Miembro NORD
Correo electrónico: [email protected]
Enfermedades raras relacionadas: Trastorno de Haploinsuficiencia SETBP1
https://rarediseases.org/es/organizations/setbp1-society/
Ver perfil >
Severe Chronic Neutropenia International Registry
Teléfono: 206-543-9749 Correo electrónico: [email protected] Fax: 206-543-3668
https://rarediseases.org/es/organizations/severe-chronic-neutropenia-international-registry/
Ver perfil >
Sexuality Information and Education Council of the U.S.
Teléfono: 212-819-9770 Correo electrónico: [email protected] Fax: 212-819-9776
Enfermedades raras relacionadas: Bowenoid Papulosis, Proctitis
https://rarediseases.org/es/organizations/sexuality-information-and-education-council-of-the-u-s/
Ver perfil >
  1. «
  2. 1
  3. ...
  4. 37
  5. 38
  6. 39
  7. 40
  8. 41
  9. 42
  10. 43
  11. ...
  12. 48
  13. »
  • For Patients & Caregivers
  • For Organizations
  • For Clinicians & Researchers
Sign Up for NORD News

NORD Patient Hotline

NORD's Helpline is here for you. Reach us at 1-800-999-6673 or visit Contact Us.

Helpline hours:
Monday–Thursday 8:30am–7:00pm ET
Friday 8:30am–6:00pm ET

NORD Headquarters

120 Longwater Drive
Suite 105
Norwell, MA 02061

Mailing Address

7 Kenosia Avenue
Danbury, CT 06810
Phone: 203-744-0100
Fax: 203-263-9938

Donation Mailing Address

NORD, Inc. – Donations
Dept. 5930
P.O. Box 4110
Woburn, MA 01888

Other Locations

Washington, DC Office
1779 Massachusetts Avenue
Suite 500
Washington, DC 20036
  • Understanding Rare Disease
    • Where to Start
    • Stay Informed
    • Patient Stories
  • Living with a Rare Disease
    • Manage Your Care
    • We Can Help
  • Community Support
    • Where to Start
    • Mentoring Organizations
    • Improving Clinical Care
    • Partnering With the Community
    • Community Support
  • Advancing Research
    • For Patients
    • For Researchers
    • For Clinicians
    • Connect
    • Publications
    • Download a Subset of NORD’s Rare Disease Database
  • Driving Policy
    • NORD Policy Priorities
    • Taking Action
    • Join the Rare Action Network®
  • Donate
    • Donate
  • Get Involved
  • Legal
    • Brand Resources and Guidelines
    • Terms & Conditions
    • Privacy Policy
  • Rare Disease News
  • About Us
  • Media Inquiries
  • Get Involved
  • Careers at NORD
  • Sitemap
  • Contact Us

Copyright ©2026 NORD – National Organization for Rare Disorders, Inc. All rights reserved.

NORD is a registered 501(c)(3) charity organization.
Please note that NORD provides this information for the benefit of the rare disease community. NORD is not a medical provider or health care facility and thus can neither diagnose any disease or disorder nor endorse or recommend any specific medical treatments. Patients must rely on the personal and individualized medical advice of their qualified health care professionals before seeking any information related to their particular diagnosis, cure or treatment of a condition or disorder.

2023TRbadge_lg Platinum_Transparency_2024 Four_Stars_Charity

Make 2026 Count: Gift research, care, and advocacy for families everywhere

Your gift today fuels progress in the lab, in clinics, on Capitol Hill and for rare families who can’t wait another year for answers.


  • Donor-Advised Funds
  • Donate Stock
  • Planned Giving
NORD logo for Rare Disorders site.