• Alliance/Advocacy Organizations

• 271.

NTM Info & Research, Inc.

#NTMir Non-profit organization dedicated to patient support, medical education & research for people with nontuberculous mycobacterial lung disease (#NTM).

• Nerve, Muscle, and Bone Diseases

• 272.

THE XLH NETWORK INC

The Official Facebook Page of The XLH Network, Inc.

• Alliance/Advocacy Organizations

• 273.

Cystinosis Research Network, Inc.

Cystinosis Research Network is dedicated to supporting research, providing family outreach & educating the public & medical communities about #cystinosis The Cystinosis Research Network is an all-volunteer, non-profit organization dedicated to supporting and advocating cystinosis research.

• Birth Defects, Genetic Diseases

• 274.

Hoppys Hope To End Huntingtons Disease

RAISE AWARENESS AND PROVIDE FINANCIAL SUPPORT TO ORGANIZATIONS DEDICATED TO FINDING TREATMENTS, AND ULTIMATELY, A CURE FOR HUNTINGTON'S DISEASE.

Cancer Genomics Consortium

The CGC represents clinical cytogeneticists, molecular geneticists, and molecular pathologists to promote best practices & education in clinical cancer genomics The CGC is focused on education and promoting best practices in clinical cancer genomics.

American Behcet's Disease Association (ABDA)

Bringing national focus, advocacy, research and awareness of Behcet's Disease Support.

HEMOPHILIA OF GEORGIA INC

A nonprofit organization providing services and support for Georgians who have hemophilia, von Willebrand Disease, and other bleeding disorders.

• Specifically Named Diseases

• 278.

Watch 4 Wegeners

It could save a life. Home Sarahx27s Story About Our Board Contact Us Run To Raise Testimonials More Watch 4 Wegeners It Could Save a Life Our daughter Sarah River Whitmire was a college student in pharmacy school when she died suddenly at age 20 from complications of undiagnosed Granulomatosis with Polyangiitis GPA also known as Wegener39s Disease a rare autoimmune disease that no one knew she had.

• Fund Raising and/or Fund Distribution

• 279.

BFLS Incorporated

Mom on a mission to raise awareness and funds for research for the rare genetic disorder Börjeson-Forssman-Lehman Syndrome or BFLS� Born Fierce.