• Other Medical Research N.E.C.

• 190.

Human Growth Foundation

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

CURE 4 THE KIDS FOUNDATION

Treating & preventing childhood catastrophic diseases, cancer & blood disorders.

Spina Bifida Resource Network

To empower disabled people to challenge perceptions, embrace interdependence & live their best lives.

• Fund Raising and/or Fund Distribution

• 193.

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

• 194.

Jansen De Vries Syndrome Foundation

The Jansen de Vries Syndrome (JdVS) Foundation is a nonprofit, tax-exempt organization as defined in section 501(c)(3) of the Internal Revenue Code and, as such, contributions to JdVS Foundation are tax-deductible.

• Patient Services�Entertainment, Recreation

• 195.

Idefine Inc

IDefine is committed to identifying life-changing treatments & cures and building community for those with Kleefstra Syndrome and intellectual disabilities.

• Fund Raising and/or Fund Distribution

• 196.

DHPS FOUNDATION

Leading the way in DHPS Deficiency Disorder research and education in order to find treatment, and a cure #curedhps #raredisease Our genetics make us unique our struggles and triumphs unite us.

• Public Foundations

• 197.

The Mathew Forbes Romer Foundation Inc

Education & Research of Children's Genetic Diseases of the Brain MFRF was founded in South Florida in 1998 with a mission to prevent and eventually cure fatal children's genetic diseases of the brain.

• Nonmonetary Support N.E.C.*

• 198.

SOPHIA'S FUND INC

Fighting childhood cancer on all fronts by raising awareness and research funding, as well as supporting families affected by pediatric cancer financially.