Insights

Digital Engagement The company maintains an active online presence with a website and quarterly newsletter, indicating an audience that is engaged through digital channels, providing opportunities to offer digital tools, content management solutions, or targeted advertising services.

Funding Potential With a revenue range of 1 million to 10 million dollars, the organization may be interested in philanthropic grants, corporate sponsorships, or technology solutions that streamline fundraising efforts and donor management for non-profits.

Community Outreach As a non-profit fostering a global community for families affected by Alagille Syndrome, there is potential for partnerships in community engagement platforms, event management solutions, or community health tech products.

Research Support The organization funds research and encourages participation in studies, suggesting opportunities for laboratory tools, research data management, or clinical trial technology providers to support their mission.

Technology Stack Utilizing modern web technologies such as Webpack, dc.js, and hCaptcha indicates openness to innovative online solutions, suggesting potential for collaboration on website optimization, security services, or data visualization tools tailored for non-profits.

Alagille Syndrome Alliance Tech Stack

Alagille Syndrome Alliance uses 8 technology products and services including Google Hosted Libraries, oEmbed, Webpack, and more. Explore Alagille Syndrome Alliance's tech stack below.

  • Google Hosted Libraries
    Content Delivery Network
  • oEmbed
    Dev Tools
  • Webpack
    Development
  • dc.js
    Javascript Graphics
  • Modernizr
    Javascript Libraries
  • hCaptcha
    Security
  • Piwik PRO Core
    Web Analytics
  • Max Mega Menu
    Widgets

Media & News

Alagille Syndrome Alliance's Email Address Formats

Alagille Syndrome Alliance uses at least 1 format(s):
Alagille Syndrome Alliance Email FormatsExamplePercentage
First@alagille.orgJohn@alagille.org
50%
First.Last@alagille.orgJohn.Doe@alagille.org
50%

Frequently Asked Questions

Where is Alagille Syndrome Alliance's headquarters located?

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Alagille Syndrome Alliance's main headquarters is located at 1012 14th Street Northwest Suite 500 Washington, District of Columbia United States. The company has employees across 1 continents, including North America.

What is Alagille Syndrome Alliance's phone number?

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You can contact Alagille Syndrome Alliance's main corporate office by phone at . For more prospecting data, LeadIQ has access to up-to-date and accurate contact information within our platform. Find, capture, and sync contact data to your CRM and sales tools in one click.

What is Alagille Syndrome Alliance's official website and social media links?

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Alagille Syndrome Alliance's official website is alagille.org and has social profiles on LinkedIn.

What is Alagille Syndrome Alliance's SIC code NAICS code?

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Alagille Syndrome Alliance's SIC code is 8621 - Professional Membership Organizations NAICS code is 813 - Religious, Grantmaking, Civic, Professional, and Similar Organizations.

How many employees does Alagille Syndrome Alliance have currently?

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As of March 2026, Alagille Syndrome Alliance has approximately 8 employees across 1 continents, including North America. Key team members include President: R. S.Founder: C. L. A. M.Executive Director: C. B.. Explore Alagille Syndrome Alliance's employee directory with LeadIQ.

What industry does Alagille Syndrome Alliance belong to?

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Alagille Syndrome Alliance operates in the Non-profit Organizations industry.

What technology does Alagille Syndrome Alliance use?

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Alagille Syndrome Alliance's tech stack includes Google Hosted LibrariesoEmbedWebpackdc.jsModernizrhCaptchaPiwik PRO CoreMax Mega Menu.

What is Alagille Syndrome Alliance's email format?

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Alagille Syndrome Alliance's email format typically follows the pattern of First@alagille.org. Find more Alagille Syndrome Alliance email formats with LeadIQ.

When was Alagille Syndrome Alliance founded?

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Alagille Syndrome Alliance was founded in 1993.

Alagille Syndrome Alliance

Non-profit OrganizationsDistrict of Columbia, United States2-10 Employees

"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.

Section iconCompany Overview

Headquarters
1012 14th Street Northwest Suite 500 Washington, District of Columbia United States
Phone number
SIC Code
8621 - Professional Membership Organizations
NAICS Code
813 - Religious, Grantmaking, Civic, Professional, and Similar Organizations
Founded
1993
Employees
2-10

Section iconMedia & News

Section iconFunding & Financials

  • $1M$10M

    Alagille Syndrome Alliance's revenue is estimated to be in the range of $1M$10M

Section iconFunding & Financials

  • $1M$10M

    Alagille Syndrome Alliance's revenue is estimated to be in the range of $1M$10M

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