• Birth Defects, Genetic Diseases Research

• 172.

The Evanosky Foundation

The Evanosky Foundation exists for the purpose of generating funds to support two main objectives.

NEW ENGLAND CONNECTION FOR PKU AND ALLIED DISORDERS INC

Volunteer, nonprofit, striving to be a supportive resource for New England area families and friends affected by inborn errors of metabolism, such as PKU.

• Fund Raising and/or Fund Distribution

• 174.

EBSTEINS ANOMALY FOUNDATION INC

The goal of the Ebstein's Anomaly Foundation is to fund research in order to advance the diagnosis, treatment and prevention of this rare congenital heart defect.

• Alliance/Advocacy Organizations

• 175.

Lynch Syndrome International

MISSION STATEMENTThe primary mission of Lynch Syndrome International (LSI) is to serve our global communities by focusing on providing support for individuals afflicted with Lynch syndrome, creating public awareness of the syndrome, educating members of the general public and health care professionals and providing support for Lynch syndrome research endeavors.

• Specifically Named Diseases Research

• 176.

PROJECT ALIVE

A Hunter syndrome research and advocacy foundation.

Cure KCNH1 Foundation

Cure KCNH1 Foundation is dedicated to advancing the development of treatments for children with KCNH1 genetic disorders.

Texas Neurofibromatosis Foundation

We’re a community of NF patients, parents, doctors and advocates who want to listen, support or help you as we can.

• Specifically Named Diseases

• 179.

Eds Resource Network

EDS Resource Network (EDSRN), a 501(c)(3) nonprofit of Utah, provides aid, education, and support to the Ehlers-Danlos Syndromes (EDS) patients, caregivers, and medical providers across the state.

• Epilepsy Research

• 180.

Shay Emma Hammer Research Foundation

We’re working to document the first 1000 cases of SCN8A gene variants and connect families Advancing epilepsy awareness.