The National Organization for Rare Disorders (NORD)


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Index of Rare Diseases

This is the list of diseases currently covered in the Rare Disease Database.

Rare Disease Database

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Index of Organizations

This is the list of organizations in NORD’s Organizational Database.

Organizational Database

Read about more than 2,000 patient organizations and other sources of help.

NORD's
Washington Office

NORD's Washington OfficeRead about events on Capitol Hill, funding for rare-disease research, and other topics of interest from NORD's office in Washington, DC.

 

**IMPORTANT** The information contained in the Organizational Database (ODB) is provided for informational purposes only. There is no implied endorsement by NORD. NORD does not promote or endorse participation in any specific organization. The information is subject to change without notice. Every effort is made to ensure that the details for each entry are as current as possible.

Ambiguous Genitalia Support Network
a/k/a:   AGSN

Address:
P.O. Box 313
Clements, CA 95227-0313
USA

800 Number: --
TDD: --
Email Address: agsn@inreach.com

The Ambiguous Genitalia Support Network is a voluntary health organization consisting of affected individuals, parents, other family members, and professionals. Established in 1994, the Ambiguous Genitalia Support Network is dedicated to providing information, assistance, and support to families of children diagnosed with ambiguous genitalia. Ambiguous genitalia are those in which it is difficult to classify the infant as male or female. The group/network is made up of parents, families, and professionals, all with the common goal of making educated and informed decisions about children's health, medical care, and well-being related to intersex conditions.

Chapters: 1


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Last modified Wednesday, November 26, 2008