• Alliance/Advocacy Organizations

• 127.

Wilson Disease Association

Wilson disease is a genetic disorder of having excessive copper accumulation in the liver or brain that is fatal unless detected and treated Welcome to the official fan page of The Wilson Disease Association International.

• Other Medical Research N.E.C.

• 128.

Human Growth Foundation

Our vision is that everyone with a rare growth, bone, and endocrine condition can access the best care possible.

• Single Organization Support

• 129.

Mountain Park Health Centerfoundation

MOUNTAIN PARK HEALTH CENTER FOUNDATION IS THE PHILANTHROPIC ARM OF MOUNTAIN PARK HEALTH CENTER.

• Fund Raising and/or Fund Distribution

• 130.

Mayberry Memorial

Cancer awareness and research support Estimates suggest that every 1 in 300 individualshas a gene mutation that is associated with Lynch Syndrome.

• Fund Raising and/or Fund Distribution

• 131.

Ellie White Foundation for Rare Genetic Disorders Inc

We will not give up until a cure for Wolfram syndrome is found for Ellie and the children suffering from this disorder.

• Alliance/Advocacy Organizations

• 132.

Stargardtians Inc

Our mission is to raise awareness of Stargardt’s Disease and to create opportunities for people living with Stargardt’s to further their education and develop their own business.

• Fund Raising and/or Fund Distribution

• 133.

Life for Liam and Friends Foundation

Mission to support families who are impacted by NPC and help find a cure through connecting NPC families, spreading awareness, and supporting medical research.

Action for Aidan

Please Help Us to Raise Money for Hunter Syndrome research.

• Fund Raising and/or Fund Distribution

• 135.

The Children's Rare Disorders Fund

Dedicated to curing rare genetic disorders Founded in July 2022 by parents of a toddler affected by FOXG1, The CRD Fund focuses on under served communities in the rare disorder space.