Alport Syndrome Foundation Inc

Improving patient lives through education, empowerment, advocacy, and research with a vision to conquer #Alportsyndrome.

• Birth Defects, Genetic Diseases Research

• 173.

Kate Foundation for Rett Syndrome Research Inc

The Kate Foundation is a 501(c)(3) organization dedicated to raising research funding for the reversal of Rett Syndrome and related disorders.

• Birth Defects, Genetic Diseases

• 174.

Gene Spotlight Inc

We are a nonprofit medical research and advocacy organization committed to spark breakthroughs in treatments and cures for rare genetic disorders, including lysosomal storage diseases, uncommon cancers and other orphan diseases.

• Specifically Named Diseases

• 175.

CADASIL Association

cureCADASIL is a non-profit organization committed to curing #CADASIL and improving the quality of life for those affected by this genetic disease.

Alpha-1 Foundation, Inc.

Our mission is to increase awareness of and find a cure for Alpha-1 Antitrypsin Deficiency.

• Specifically Named Diseases Research

• 177.

PROJECT ALIVE

A Hunter syndrome research and advocacy foundation.

• Birth Defects, Genetic Diseases

• 178.

Tatton Brown Rahman Syndrome Community Inc

The Tatton Brown Rahman Syndrome Community supports research and educates individuals with TBRS and their families, friends, and service providers.

• Birth Defects, Genetic Diseases Research

• 179.

Project Guardian

Project GUARDIAN Genomic Uniformscreening Against Rare Diseases In All Newborns Recent Interviews see more Revolutionizing Healthcare Dr.

• Philanthropy/Charity/ Voluntarism Promotion (General)

• 180.

HOPEFUL HALOS FOUNDATION

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