• Other Philanthropy, Voluntarism, and Grantmaking Foundations N.E.C.

• 136.

INTERNATIONAL CHILDRENS ANOPHTHALMIA NETWORK INC

ICAN a voluntary not for profit organization, is a group of families and professionals dedicated to lending support to individuals who want to learn more about microphthalmia and anopthalmia and associated genetic counseling.

• Scholarships, Student Financial Aid, Awards

• 137.

Arm Foundation for Regenerative Medicine Education & Research

The primary international resource for education and research related to the advancement and acceptance of ethical cell and gene medicine.

• Epilepsy

• 138.

Cure Ahc Foundation

Alternating Hemiplegia of Childhood (AHC) is a complex, ultra-rare neurological disease.

• Research Institutes and/or Public Policy Analysis

• 139.

Riaan Research Initiative Inc

501(c)(3) non-profit organization hunting for a cure for rare and life-limiting genetic diseases that hurt children, starting with Cockayne syndrome.

Rare New England Inc

Rare New England's Mission is to bring together New England patients and families touched by rare and complex disorders.

• Alliance/Advocacy Organizations

• 141.

Allo Hope Foundation

Our mission is to prevent any harm, stillbirth or infant death caused by #Alloimmunization and Hemolytic Disease of the Fetus and Newborn (#HDFN) Our mission is to prevent harm, stillbirth and infant death caused by alloimmunization and HDFN.

FANCONI CANCER FOUNDATION

At the Fanconi Cancer Foundation, our mission is to improve the lives of people affected by Fanconi anemia and associated cancers worldwide by funding exceptional research and empowering our community.

• Specifically Named Diseases

• 143.

Project CASK

An innovative rare disease non-profit driving breakthroughs in treatments and a cure for CASK gene disorders.

• Medical Specialty Research

• 144.

Curemapk8Ip3 Foundation

Family support network for patients and their families affected by a gene mutation in MAPK8IP3 Page for individuals and families with gene variant MAPK8IP3 Improve the lives of patients and families affected by a MAPK8IP3 gene mutation by performing the following activities: raising community awareness of MAPK8IP3-Related Neurodevelopmental Disorder; facilitating research of MAPK8IP3-Related Neurodevelopmental and related Disorders; collecting and disseminating information and resources relating to MAPK8IP3-Related Neurodevelopmental and related Disorders; supporting those affected by MAPK8IP3-Related Neurodevelopmental and related Disorders; and any other charitable educational or scientific activities that are in furtherance of the Corporation's purposes.