Insights

Lean Ops The Alagille Syndrome Alliance operates with a small team of 2 to 10 staff and reaches families worldwide through a quarterly newsletter and a website, signaling strong return on investment from scalable donor management and automation that can extend impact without adding substantial headcount.

Digital Enablement With a tech stack including Cloudflare, Google Analytics, and modern web tooling, the organization is well positioned to optimize its online experience, implement data driven donor communications, and enhance secure hosting; opportunities exist for dashboards, marketing automation, and performance improvements.

Research Partnerships Active funding of research and encouragement of member participation create opportunities for patient registry solutions, study recruitment platforms, and grant management tools to accelerate research collaborations and donor engagement.

Global Reach Global reach to families worldwide suggests a need for multilingual content, localization, and accessible design to broaden outreach, donor conversion, and information access through translation, CMS localization, and accessibility audits.

Security and Compliance Online fundraising and health related information imply ongoing needs for secure donation processing, privacy compliance, and accessibility; potential fits include PCI compliant payments, privacy assessments, and security hardening services.

Alagille Syndrome Alliance Tech Stack

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

  • Cloudflare
    Content Management System
  • Webpack
    Development
  • Module Federation
    Development
  • dc.js
    Javascript Graphics
  • Clipboard.js
    Javascript Libraries
  • hCaptcha
    Security
  • Google Analytics
    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 20005 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 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 June 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 CloudflareWebpackModule Federationdc.jsClipboard.jshCaptchaGoogle AnalyticsMax 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

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

Headquarters
1012 14th Street Northwest Suite 500 Washington, District of Columbia 20005 United States
Phone number
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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