• Specifically Named Diseases

• 280.

Mps6Cess Foundation

The MPS6CESS Foundation is a 501(C)(3) non-profit, all-volunteer organization dedicated to promoting awareness and support for families living with Mucopolysaccharidosis VI, or MPS VI.

• Birth Defects, Genetic Diseases

• 281.

Nergg Inc

Raise awareness and educate regarding the effects of genetics on health 1977 2025Celebrating 48 Yearsof Education Collaboration and more.

• Alliance/Advocacy Organizations

• 282.

Sickle Cell Disease Association of America, Inc.

The Sickle Cell Disease Association of America (SCDAA) serves as the nation's headquarters for sickle cell disease support and advocacy & the search for a cure.

• Alliance/Advocacy Organizations

• 283.

Hht Foundation International Inc

Cure HHT is the only organization in the US advocating for research, education and a cure for Hereditary Hemorrhagic Telangiectasia, Osler-Weber-Rendu Syndrome The official Facebook page for Cure HHT, the world's leading organization working to raise awareness The mission of the HHT Foundation International is to find a cure for HHT while saving the lives and improving the well-being of individuals and families affected by HHT.

The Global Foundation for Peroxisomal Disorders

The GFPD's mission is to improve the lives of individuals with peroxisomal disorders by funding research, championing scientific collaboration, and empowering families and professionals through educational programs and support services.

• Arthritis

• 285.

Arthritis Foundation

Here for the 1 in 4 with #arthritis. | Fighting to cure the #1 cause of disability.

Born a Hero

Born A Hero is a research foundation with a mission to accelerate innovation and research to improve the quality of life for patients with FGFR syndromes.

• Arthritis

• 287.

Arthritis Foundation Inc

Here for the 1 in 4 with #arthritis. | Fighting to cure the #1 cause of disability.

• Fund Raising and/or Fund Distribution

• 288.

NORTH CAROLINA RARE DISEASE

Rare Disease Innovations Institute Our Mission RDII is a global nonprofit focused on educating engaging and equipping the rare disease community.