• Birth Defects, Genetic Diseases

• 64.

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.

Cloves Syndrome Community

Support, Research & Education to improve the quality of life for ppl with CLOVES.

Decoding Developmental Epilepsies

We serve two distinct communities. First, we serve those living with SCN8A and their families.

• Birth Defects, Genetic Diseases

• 67.

International Rett Syndrome Association, Inc.

We are transforming lives every day in our fight to treat and cure Rett syndrome and better the lives of families living with this devastating disorder.

Foxg1 Research Foundation

FOXG1 syndrome is a childhood neurological genetic disorder and is a key to understanding many brain disorders.

• Specifically Named Diseases

• 69.

NR2F1 FOUNDATION

Empowering families and individuals living with rare #NR2F1 mutations through education, awareness and research.

• Birth Defects, Genetic Diseases Research

• 70.

ADLD CENTER

The ADLD Center is focused on raising awareness about Autosomal Dominant Leukodystrophy ADLD and developing a network of clinicians researchers patients and their caregiversadvocates in order to raise funds as we move forward towards finding a cure.

• Public Foundations

• 71.

CURING RETINAL BLINDNESS

Welcome to our mission of bringing sight to children who are blind or visually impaired due to CRB1 retinal disease.

• Patient Services�Entertainment, Recreation

• 72.

Coalition For Usher Syndrome Research

Usher Syndrome Coalition: Connecting the global Usher community.