• Health Support Services

• 289.

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.

Rare Trait Hope Fund

Rare trait Hope Fund facilitates research and provides funding for the development of treatments for a rare disease called Aspartylglucosaminuria (AGU) in hopes to save lives of AGU kids and adults.

• Birth Defects, Genetic Diseases

• 291.

Xeroderma Pigmentosum Family Support Group

The XP Family Support Group is dedicated to improving the quality of life of those with xeroderma pigmentosum.

• Alliance/Advocacy Organizations

• 292.

Gigi's Playhouse-Tampa

GiGi's Playhouse - Down Syndrome Achievement Centers.

• Medical Specialty Research

• 293.

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.

• Brain Disorders

• 294.

Initiative for Depersonalization Studies

IDS is a non-profit 501(c) corporation dedicated to the promotion of ongoing research into Depersonalization/Derealization Disorder (DDD) as well as increasing awareness of DDD through mass media, social media, and regularly scheduled conferences around the world.

CMT Research Foundation Inc

The CMT Research Foundation has one mission: Deliver treatments and cures for #CMT.

• Services to Promote the Independence of Specific Populations

• 296.

Triadd Foundation Inc

THE FOUNDATION SERVES TO EMPOWER INDIVIDUALS WITH INTELLECTUAL AND OTHER DEVELOPMENTAL DISABILITIES TO ENJOY HEALTHY AND MEANINGFUL LIVES IN THEIR COMMUNITIES THROUGH A MORE FLEXIBLE, INTEGRATED AND INNOVATIVE SYSTEM OF SUPPORTS AND SERVICES.

• Alliance/Advocacy Organizations

• 297.

Ctx Alliance NFP

Providing education, support, advocacy, and promoting research for CTX patients, their families, and medical professionals who treat and study this rare disease Providing education, support, advocacy, and promoting research for CTX patients, their families, and medical professionals who treat and study this rare disease.