Insights

Fundraising Potential Non-profit charity with annual revenue in the 1M to 10M range presents opportunities for grant writing services, donor management platforms, and fundraising strategy partnerships tailored to small to mid-sized organizations.

Community Engagement Global reach to families through newsletters and a Medical Advisory Board indicates a need for scalable donor communications, CRM solutions, and targeted content automation to enhance member engagement and retention.

Tech Stack Fit Current stack includes WordPress, Cloudflare, Google Workspace, analytics tools, and cloud hosting, suggesting upsell opportunities in website optimization, analytics-driven fundraising dashboards, and security/compliance enhancements.

Research Collaboration Funding and facilitation of research points to potential partnerships with grant management platforms, volunteer/recruitment tools, and data collection solutions to support clinical studies and patient registries.

Strategic Growth Small but globally active organization with a focused mission offers a gateway for dedicated impact solutions, including volunteer management, event coordination, and targeted awareness campaigns that align with donor and partner acquisitions.

Similar companies to Alagille Syndrome Alliance

Alagille Syndrome Alliance Tech Stack

Alagille Syndrome Alliance uses 8 technology products and services including Matomo, Cloudflare, WordPress, and more. Explore Alagille Syndrome Alliance's tech stack below.

Alagille Syndrome Alliance's Email Address Formats

Alagille Syndrome Alliance uses at least 2 email formats:
Alagille Syndrome Alliance Email FormatsExamplePercentage
First@alagille.orgJohn@alagille.org
50%
First.Last@alagille.orgJohn.Doe@alagille.org
50%

Frequently Asked Questions

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.

How much revenue does Alagille Syndrome Alliance generate?

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As of September 2026, Alagille Syndrome Alliance's annual revenue is estimated to be $1M - $10M.

What is Alagille Syndrome Alliance's NAICS code?

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Alagille Syndrome Alliance's 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 September 2026, Alagille Syndrome Alliance has approximately 8 employees across 1 continents, including North America. Key team members include President: R. S. and Executive Director: C. L. 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 Matomo, Cloudflare, WordPress, Webpack, Google Workspace, Piwik PRO Core, DigitalOcean Web Hosting and Max 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 logo

Alagille Syndrome Alliance

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

The Alagille Syndrome Alliance is a small nonprofit based in Washington, D.C., operating as a 501(c)(3) public charity. It maintains a Medical Advisory Board and publishes a quarterly newsletter, in addition to a website that reaches families worldwide. The organization acts as a central resource for people with Alagille Syndrome and for their families and friends, offering mutual support, information, and access to resources, and it promotes participation in research.

It provides up-to-date, accurate information on ALGS and its treatments and supports research by encouraging members to engage in studies. Based in Washington, District of Columbia, the alliance operates as a small nonprofit dedicated to connecting affected individuals with information and services and nurturing a community around ALGS.

Section iconCompany Overview

Phone number
NAICS Code
813 - Religious, Grantmaking, Civic, Professional, and Similar Organizations
Founded
1993
Employees
2-10

Section iconFunding & Financials

  • $1M - $10M

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

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