• Health Support Services

• 208.

International Foundation Forchildren With Craniofacial Disorder

I. F. C. C. D. Helping children with facial deformities In response to a need to help children with genetic facial malformations tumors and flesheating bacterial infections the International College for MaxilloFacial Surgery ICMFS chartered the International Foundation for Children with Cranialfacial Disorders IFCCD.

• Birth Defects, Genetic Diseases Research

• 209.

Cure CMD

Cure CMD’s mission is to advance research toward treatments for congenital muscular dystrophies and empower those living with CMD.

FAMILIAL DYSAUTONOMIA NOW FOUNDATION

FD NOW is a 501c3 non-profit organization dedicated to funding the fast-track research at the Laboratory for Familial Dysautonomia Research at Fordham University in New York, USA.

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

• 211.

Proteus Syndrome Foundation

The Proteus Syndrome Foundation, a 501c3 not-for-profit organization, is dedicated improving the lives of Proteus patients by funding AKT1 research.

Cloves Syndrome Community

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

• Fund Raising and/or Fund Distribution

• 213.

Glioblastoma Research Organization Inc

501(c)3 - Raising awareness and funds for new global, cutting-edge research to find a cure for #Glioblastoma.

Children and Family Comprehensive Health Outreach Inc

Our mission is to support and enhance community health initiatives in regards to awareness, prevention and education within the discipline of children and family in every healthcare and service facet.

Dallas Sickle Cell Organization

So much misleading information about sickle cell, the stigma stops now.

• Alliance/Advocacy Organizations

• 216.

Rare Disease Company Coalition Inc

We are a coalition of life science companies committed to discovering, developing & delivering rare disease treatments for the patients we serve.