• Birth Defects, Genetic Diseases

• 244.

Preimplantation Genetic Diagnosis International Society

Promote Research and practice in Preimplaltation Genetic Testing Preimplantation Genetic Diagnosis International Society About PGDIS Since 2002 PGDIS has coordinated research education and training in preimplantation genetic testing Next Meetings Join us at the 22nd International Conference on preimplantation genetics on April 69 2025 in Leuven Belgium Education Learn more about the handson PGT workshop for Genetic and Chromosomal Disorders for PGDIS Members Welcome To PGDIS.

• Private Grantmaking Foundations

• 245.

Jain Foundation Inc

The Jain Foundation's mission is to identify treatments for Dysferlinopathy also known as LGMD2B/R2 or Miyoshi Myopathy ORCHESTRATING A CURE FOR DYSFERLINOPATHY The Jain Foundation is singularly focused on finding a cure for dysferlinopathy also referred to as LGMD2B LGMDR2 Miyoshi Myopathy 1 ORCHESTRATINGA CURE FORDYSFERLINOPATHY The Jain Foundation is singularly focused on finding a cure for dysferlinopathy also referred to as LGMD2B LGMDR2 Miyoshi Myopathy 1 WHAT IS DYSFERLINOPATHY.

• Organ and Tissue Bank

• 246.

New Jersey Organ and Tissue Sharing Network Inc

Dedicated to saving lives through organ and tissue donation.

• Fund Raising and/or Fund Distribution

• 247.

A Toast To Carly

Home ABOUT EVENTS DONATE CONTACT More About The mission ofA Toast to Carlyis to raise funds to both eventually find a cure for the disease while also helping those living with this debilitating disease.

Ring14 USA Outreach Inc

Ring14 Syndrome, Rare disease, Rare epilepsy, nonprofit, support, advocacy, research Ring14 USA is nonprofit 501(c)(3) that supports children and families affected by the rare syndromes of the 14th chromosome, such as Ring14 syndrome.

• Medical Specialty Research

• 249.

Global Society of Rare Genitourinary Tumors Inc

International Society dedicated to improving the care of rare GU tumors through cutting edge science and the promotion of education.

• Birth Defects, Genetic Diseases Research

• 250.

International FOXP1 Foundation

Our mission is to build a global community that empowers and supports families and individuals with FOXP1 syndrome by sharing knowledge, inspiring hope, supporting research, and raising awareness.

Dlg4 Research Fund

DLG4-related Synaptopathy / SHINE Syndrome *Managed by the board of the DLG4 SHINE Foundation A page for people interested in learning more about DLG4-related Synaptopathy / SHINE Syndrome *Managed by the board of the DLG4 SHINE Foundation Mission To find specific treatment options and a cure for DLG4 patients by building a collaborative network of patients, families, clinicians and scientists that will work together to raise awareness and accelerate the understanding, diagnosis and treatment of DLG4 related synaptopathy.

• Diseases of Specific Organs

• 252.

NATIONAL FOUNDATION FOR CELIAC

Committed to finding treatments and a cure for celiac disease.