APBD RESEARCH FOUNDATION

Supporting individuals and families affected by Adult Polyglucosan Body Disease (APBD), and accelerating improved APBD diagnoses, care and treatment options.

• Fund Raising and/or Fund Distribution

• 92.

Eleanor Kaplan Foundation Inc

To raise funds and awareness to develop cures for Ultra Rare Neurodegenerative Diseases.

• Birth Defects, Genetic Diseases Research

• 93.

Alstrom Angels Corp

www. alstromangels. org Dedicated to raising funds for Alstrom Syndrome genetic and medical research, increasing awareness of the rare disease among the general public and medical communities, and improving family support for those affected by the Syndrome.

• Birth Defects, Genetic Diseases

• 94.

Kinslow Tubb4a Foundation Inc

Our mission is to provide information on accessible and equitable treatment options for every child affected by TUBB4A-related leukodystrophy, regardless of their geographical location or socioeconomic status.

• Medical Specialty Research

• 95.

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.

• Patient Services�Entertainment, Recreation

• 96.

BELIEVING FOR BRYLEIGH FOUNDATION INC

On April 2, 2013 our little girl Bryleigh was diagnosed with MLD.

• Birth Defects, Genetic Diseases

• 97.

DESSH

Join the DeSantoShinawi SyndromePATIENT REGISTRYpowered by About Us DESSH Syndrome News Events Get Involved Legal and Privacy More DESSH is short forDeSantoShinawi Syndrome.

• Specifically Named Diseases

• 98.

Raiden Science Foundation

Our Mission: Harness the power of community to develop cures for rare diseases, starting with UBA5 disorder Our Vision: Make the impossible possible for Rare* Home About Research Engage Contact Us RAIDEN SCIENCE FOUNDATION Creating more than hope giving kids suffering from UBA5 Disorder a fighting chance.

• Fund Raising and/or Fund Distribution

• 99.

GLUT1 DEFICIENCY FOUNDATION INC

Building a brighter future Bringing help and hope to the Glut1 Deficiency community as we work together to improve lives through awareness education advocacy and research Shining a light on Glut1 Deficiency Glucose Transporter Protein Type 1 Deficiency Syndrome Glut1 Deficiency is a rare genetic condition that impairs brain metabolism.