Alagille Syndrome Alliance

Alagille Syndrome Alliance

Non Profit Organization Management, Po Box 22, Collierville, Tennessee, 38027, United States, 1-10 Employees

alagille.org

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Who is ALAGILLE SYNDROME ALLIANCE

"Mobilizing resources, facilitating connections, promoting unity, and advocating for a cure to inspire, empower, and enrich the lives of people affected by Alagille Syndrome." The Alagill...

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  • Po Box 22, Collierville, Tennessee, 38027, United States Headquarters: Po Box 22, Collierville, Tennessee, 38027, United States
  • 1993 Date Founded: 1993
  • 1-10 Employees: 1-10
  • dollar-icon Revenue: $1 Million to $5 Million
  • tech-icon Active Tech Stack: See technologies

industries-icon Industry: Non Profit Organization Management

SIC SIC Code: 8621

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Frequently Asked Questions Regarding Alagille Syndrome Alliance

Answer: Alagille Syndrome Alliance's headquarters are located at Po Box 22, Collierville, Tennessee, 38027, United States

Answer: Alagille Syndrome Alliance's official website is https://alagille.org

Answer: Alagille Syndrome Alliance's revenue is $1 Million to $5 Million

Answer: Alagille Syndrome Alliance's SIC: 8621

Answer: Alagille Syndrome Alliance has 1-10 employees

Answer: Alagille Syndrome Alliance is in Non Profit Organization Management

Answer: Alagille Syndrome Alliance contact info: Phone number: Website: https://alagille.org

Answer: "Mobilizing resources, facilitating connections, promoting unity, and advocating for a cure to inspire, empower, and enrich the lives of people affected by Alagille Syndrome." The Alagille Syndrome Alliance is a 501(c)(3) public charity with a Medical Advisory Board, a quarterly newsletter and web site that reachs families worldwide. We provide a vital link between families and offer them the resources they need to help their children live longer and healthier lives. The ALGSA is the primary resource for people with ALGS, their families and friends who form a close-knit community to provide mutual support, share information, and connect to resources. As the source of current, accurate information on ALGS and its treatment, we provide financial support for research and are actively involved in encouraging our members to participate in research studies.

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