Insights

Niche nonprofit Target the Alagille Syndrome Alliance as a focused nonprofit with global reach and a medical advisory board, offering partnerships for patient resources, research funding, and awareness campaigns.

Research collaboration Opportunity to propose sponsored research initiatives, clinical study participation drives, and grant-funded projects aligned with ALGS, leveraging their role as a primary information hub.

Community engagement Leverage their quarterly newsletter and worldwide family network to distribute educational programs, fundraising campaigns, and donor stewardship initiatives that resonate with their audience.

Technology stack Engage through their web infrastructure and content platforms (PHP, frontend tooling) to propose cost-effective digital fundraising, event portals, or member-portal enhancements.

Funding potential Position near-term sponsorship and matched-giving opportunities given their revenue range and focus on patient outcomes, research support, and global awareness.

Alagille Syndrome Alliance Tech Stack

Alagille Syndrome Alliance uses 8 technology products and services including jsDelivr, Module Federation, Webpack, and more. Explore Alagille Syndrome Alliance's tech stack below.

  • jsDelivr
    Content Delivery Network
  • Module Federation
    Development
  • Webpack
    Development
  • Element UI
    Javascript Frameworks
  • Underscore.js
    Javascript Libraries
  • PHP
    Programming Languages
  • Google Search Console
    Web Analytics
  • Max Mega Menu
    Widgets

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

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 August 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 August 2026, Alagille Syndrome Alliance has approximately 8 employees across 1 continents, including North America. Key team members include President: R. S.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 jsDelivrModule FederationWebpackElement UIUnderscore.jsPHPGoogle Search ConsoleMax 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

Section iconFunding & Financials

  • $1M - $10M

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

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