• Alliance/Advocacy Organizations

• 343.

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.

Hereditary Disease Foundation

The official Twitter feed of the Hereditary Disease Foundation.

Henrietta Lacks Foundation Inc

Established in 2010 by Rebecca Skloot, author of The Immortal Life of Henrietta Lacks, the Foundation provides financial assistance to those who've made important contributions to scientific research without consent.

• Remedial Reading, Reading Encouragement

• 346.

Firefly Fund

A nonprofit that provides crucial support for research and education necessary to accelerate cures for rare genetic diseases that affect children.

• Fund Raising and/or Fund Distribution

• 347.

BATTEN DISEASE SUPPORT AND RESEARCH ASSOCIATION

Batten Disease Support, Research, & Advocacy.

• Alliance/Advocacy Organizations

• 348.

ALVEOLAR CAPILLARY DYSPLASIA ASSOCIATION

This ACDA site is the social media outreach for parents of ACD patients during any treatment phase and support system for those experiencing child loss.

Dallas Sickle Cell Organization

So much misleading information about sickle cell, the stigma stops now.

• Neurology, Neuroscience

• 350.

VWM FAMILIES FOUNDATION INC

The VWM Families Foundation supports awareness, research efforts and families suffering with Vanishing White Matter disease (VWM).

• Fund Raising and/or Fund Distribution

• 351.

A KEY FOR A CURE FOUNDATION

Key For A Cure raises funds to directly support innovative pediatric cancer research that will lead to more effective treatments for children with cancer.