• Public Health Programs

• 316.

Norrie Disease Association NFP

NORRIE DISEASE ASSOCIATIONProviding support and leadership to the Norrie community The NDA is a diverse organization eager to serve individuals with Norrie Disease ND as well as their families social circles educators employers and medical professionals.

• Alliance/Advocacy Organizations

• 317.

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.

• Religious Related, Spiritual Development N.E.C.

• 318.

Ancient Free & Accepted Masons of Oklahoma

To develop and implement programs to assist the lodges in becoming more visible and active in the communities and to promote Friendship, Morality and Brotherly Love throughout the state.

• Religious Related, Spiritual Development N.E.C.

• 319.

Ancient Free & Accepted Masons of Oklahoma

To develop and implement programs to assist the lodges in becoming more visible and active in the communities and to promote Friendship, Morality and Brotherly Love throughout the state.

• Religious Related, Spiritual Development N.E.C.

• 320.

Ancient Free & Accepted Masons of Oklahoma

To develop and implement programs to assist the lodges in becoming more visible and active in the communities and to promote Friendship, Morality and Brotherly Love throughout the state.

• Birth Defects, Genetic Diseases Research

• 321.

Ataxia Telangiectasia Children's Project, Inc.

The A-TCP organizes & supports innovative research to optimize disease management strategies, develop new treatments and find a cure for ataxia-telangiectasia.

• Fund Raising and/or Fund Distribution

• 322.

Sdhb Coalition Inc

Our mission is to educate healthcare professionals and patients on the SDHB genetic germline mutation as well as its role and impact in this orphan disease SEE SCHEDULE O ABOVE Vision Mission Our mission is to educate healthcare professionals and patients on the SDHB genetic germline mutation as well as its role and impact in this orphan disease namely Pheochromocytoma and Paraganglioma.

WIEDEMANN-STEINER SYNDROME FOUNDATION

The Wiedemann-Steiner Syndrome Foundation provides education, fosters community, and stimulates research to improve the lives of everyone impacted by #WSS.

• Nerve, Muscle, and Bone Diseases

• 324.

Sosort

https://t. co/yU4rW8obiQ International Society on Scoliosis Orthopaedic and Rehabilitation Treatment The organization aims to promote the field of non-surgical treatment of spinal deformities such scoliosis.