• Museums & Museum Activities

• 226.

Prader Willi Association of New England Inc

PWS is a non-inherited genetic disorder which is associated with a random deletion of the 15th chromosome.

• Single Organization Support

• 227.

INTERNATIONAL WAGR SYNDROME ASSOCIATION

The IWSA represents more than 350 members in 45 countries around the world The mission of the International WAGR Syndrome Association is to promote awareness, stimulate research, and support families affected by WAGR syndrome.

• Fund Raising and/or Fund Distribution

• 228.

HUNTER SYNDROME FOUNDATION

The Hunter Syndrome Foundation is a 501(c)3 non-profit corporation with a mission to fund potential therapies that will ultimately find a cure for this disorder.

• Specifically Named Diseases Research

• 229.

The Snow Foundation

A voice for rare disease, working towards a cure for Wolfram syndrome and developing novel therapies for diabetes, vision loss, hearing loss neurodegeneration.

Kcnq2 Cure Alliance Inc

Our promise is to educate and to advance research leading to treatments or a cure for patients living with the genetic disorder KCNQ2 Raising awareness, educating, and advancing research for KCNQ2 Developmental and Epileptic Encephalopathy.

Rare New England Inc

Rare New England's Mission is to bring together New England patients and families touched by rare and complex disorders.

CureGRIN Foundation

CureGRIN is a parent-run foundation committed to improving the lives of people living with GRI disorder.

• Fund Raising and/or Fund Distribution

• 233.

Better Future 4 U

501(c)(3) nonprofit who’s mission is to fund research that leads to a treatment for individuals with HNRNPU A nonprofit organization looking to create a better future for those affected by HNRNPU and where a treatment for this rare genetic disorder is found.

• Birth Defects, Genetic Diseases

• 234.

Irf2Bpl Foundation

Raising Awareness and Research Funds for IRF2BPLDisorder This website provides the information onIRF2BPLrelated disorders for patients family members physicians and biomedical scientists working all together to solve the medical mystery on IRF2BPL.