• Birth Defects, Genetic Diseases Research

• 64.

Kate Foundation for Rett Syndrome Research Inc

The Kate Foundation is a 501(c)(3) organization dedicated to raising research funding for the reversal of Rett Syndrome and related disorders.

• Nonmonetary Support N.E.C.*

• 65.

Kidz1Stfund Inc

Established by Coach Jimbo Fisher & Candi Fisher after their son was diagnosed with Fanconi anemia.

Prader-Willi Syndrome Association | USA

What’s YOUR story. Tweet us and tell us what it’s like #GrowingUpRare We hope you will suggest the PWSA | USA facebook page to your friends.

• Specifically Named Diseases

• 67.

Pmd Foundation A New Jersey Non Profit Corporation

#Research #Awareness #Advocacy & #FamilySupport for those with #PelizaeusMerzbacherDisease #PMD #newbornscreening #raredisease #leukodystrophy #myelin The PMD Foundation is a 501(c)3 non-profit organization formed to serve three distinct interest groups as they relate to Pelizaeus-Merzbacher Disease: The Children and Families, the General Public, the Researchers and Clinicians.

• Fund Raising and/or Fund Distribution

• 68.

Tbc1D24 Foundation

Tbc1d24 foundation is a research organization and connecting site for caregivers, families, and those diagnosed with Tbc1d24 mutations.

• Birth Defects, Genetic Diseases Research

• 69.

Channeling Hope Foundation

Channeling Hope Foundation A community of researchers and families driven to advance care and develop treatments for those affected by NALCNrelated disorders.

United MSD Foundation

Our mission is simple, yet powerful: To cure Multiple Sulfatase Deficiency.

• Specifically Named Diseases Research

• 71.

THE FOCUS FOUNDATION INC

OUR FOCUS:Helping children who have* X & Y Variations* Dyslexia * DyspraxiaEarly Identification + Tar Early Awareness Detection Treatment for X Y Chromosomal Variation Disorders X Y Chromosomal Disorders 47 XXY 47 XYY 47 XXX Learn more about them.

• Professional Societies & Associations

• 72.

NOONAN SYNDROME FOUNDATION

Noonan Syndrome (NS) is the most common syndrome you've never heard of.