• Birth Defects, Genetic Diseases Research

Fam177a1 Research Fund

Founder and President, FAM177A1 Research Fund The mission of the FAM177A1 Research Fund is to improve the lives of those affected by FAM177A1 Associated Disorder through research and development of transformative therapies.

Beck Fahrner Syndrome Foundation

Our mission is to accelerate full spectrum research to cure Beck-Fahrner Syndrome (TET3 deficiency) and to empower affected families with information, knowledge, and connectivity.

Foxg1 Research Foundation

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

• Specifically Named Diseases

SETBP1 Society

President of SETBP1 Society and Parent Advocate for SETBP1-HD SETPB1 Society's mission is to provide support to individuals with SETBP1 haploinsufficiency disorde Our Mission is to provide support to individuals with SETBP1 disorder and their families, to promote discussion and fund research, and to bring awareness and education to the public.

• Fund Raising and/or Fund Distribution

Arid1B Research Foundation

Accelerating the development of disease-modifying treatments for #ARID1B-RD (haploinsufficiency) - the most frequently mutated gene in de novo NDDs (ASD, ID).

• Birth Defects, Genetic Diseases

Irf2Bpl Foundation

Raising Awareness and Research Funds for IRF2BPLDisorder This website provides the information onIRF2BPLrelated disorders for patients family members physicians and biomedical scientists working all together to solve the medical mystery on IRF2BPL.

• Specifically Named Diseases

NR2F1 FOUNDATION

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

• Public Foundations

US Mef2C Foundation Inc

To accelerate R&D to find treatments and a cure for individuals with MEF2C related disorders, and to provide support to the MEF2C Community.

• Specifically Named Diseases

YBRP Inc

YBRP is a non-profit organization whose mission is to positively impact the lives of individuals with HNRNPH2 genetic variations.

• Alliance/Advocacy Organizations

Finding Nori Foundation

The Finding Nori Foundation Home About Meet the Team Finding Joy Blog Resources Publications DONATE Contact Upcoming Events More Raising research funding for PAX5 and ALG13 related neurological disordersEmpowering families with ultra rare undiagnosed diseases to find answers Our Mission Our mission is to advance scientific research through fundraising and advocacy for ultra rare undiagnosed genetic disorders.