• American Liver Foundation

• American Society for Deaf Children

• Association for Glycogen Storage Disease

• Bloom Syndrome - BloomSyndrome.org

• Canavan Disease - The Canavan Research Foundation

• Children Living with Inherited Metabolic Diseases

• Cystic Fibrosis - The Cystic Fibrosis Foundation

• Familial Dysautonomia - Center for Jewish Genetics

• Familial Dysautonomia Hope Foundation

• Fanconi Anemia

• Fragile X Syndrome- FragileXSyndrome.org

• Galactosemia - Parents of Galactosemic Patients

• Gauchers Disease -The Gauchers Association

• Gauchers-Disease - The Mayo Clinic

• Glycogen Storage Disease Type II (Pompe Disease) Acid Maltase Deficiency Association

• Hearing Loss Association of America

• Jewish Genetic Disease Consortium

• Loeys-Dietz Syndrome - The Loeys-Dietz Syndrome Foundation

• Long Q-T Syndrome - MD Junction

• Marfan Foundation

• Maple Syrup Urine Disease Type 1B -Maple Syrup Urine Disease Family Support Group

• Megan Foundation

• Mucolipidosis - Center for Jewish Genetics

• National Association for the Deaf

• National PKU Alliance

• Niemann-Pick Disease - The National Niemann Pick Disease Foundation Inc.

• Non-Syndromic Hearing Loss

• OTC Deficiency - The National Urea Cycle Disorders Foundation

• Pendred Syndrome - American Society for Deaf Children

• Phenylketonuria - Children’s PKU Network

• Rare Diseases Clinical Research Network

• Sickle Cell Anemia

• Spinal Muscular Atrophy

• Tay-Sachs - National Tay-Sachs and Allied Diseases association

• Thalassemia

• Thalassemia Support Foundation

• Usher’s Syndrome - Usher Syndrome Coalition

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