Organizations: X

  • Xeroderma Pigmentosum Family Support Group (updated on 12/02/2009)
    The Xeroderma Pigmentosum (XP) Family Support group exists to improve the quality of life persons of those persons with XP and other diagnosed UV light conditions
  • Xeroderma Pigmentosum Society, Inc. (updated on 12/02/2009)
    The XP Society mission includes education, protection, and research for a cure for patients with XP and all severe life-threatening UV sensitivity disorders.
  • XLH Network, Inc. (updated on 08/25/2011)
    The XLH Network’s mission is to facilitate research, education, and advocacy for XLH by creating resources and a community for affected families, educating and supporting physicians and other providers of medical care, and fostering the search for a cure.
  • XLP Research Trust (updated on 11/24/2009)
    The XLP Research Trust exists to (1) Promote and fund research into the cause, management, symptoms and cure for XLP (2) Provide a point of contact and support for those families affected by XLP (3) Raise the awareness of XLP amongst the medical profession and the general public
  • XXYY Project (updated on 12/02/2009)
    To build the capacity of parents and service providers to help males with XXYY Syndrome to lead purposeful, productive lives.
Combined Federal Campaign (CFC)
#80146
4301 Connecticut Avenue NW - Suite 404
Washington, DC 20008-2369
Tel: 202.966.5557 Fax: 202.966.8553
info@geneticalliance.org