Smith-Lemli-Opitz Foundation

The Smith-Lemli-Opitz Foundation is a non-profit organization dedicated to supporting families, individuals and professionals dealing with Smith-Lemli-Opitz.

• Birth Defects, Genetic Diseases Research

• 461.

Kate Foundation for Rett Syndrome Research Inc

The Kate Foundation is a 501(c)(3) organization dedicated to raising research funding for the reversal of Rett Syndrome and related disorders.

• Epilepsy Research

• 462.

Bridge the Gap

SYNGAP1 Foundation is a legacy page dedicated to preserving the work and mission of our 100% charitable nonprofit in the USA, focused on #SYNGAP1 To serve, educate and fund research for families coping with the effects of SYNGAP mutations.

• Specifically Named Diseases

• 463.

Sotos Syndrome Support Association

Our Mission is to provide a social support environment for professionals and families of individuals affected by Sotos syndrome so they can meet, exchange ideas and help one another cope with the condition.

Dysphagia Outreach Project

Our mission is to provide meaningful assistance to individuals who are affected by dysphagia.

• Nerve, Muscle, and Bone Diseases

• 465.

CRMO FOUNDATION

Supporting CRMO patients by furthering the efforts of life-changing research, increasing access to resources and education and promoting awareness.

• Birth Defects, Genetic Diseases

• 466.

Tatton Brown Rahman Syndrome Community Inc

The Tatton Brown Rahman Syndrome Community supports research and educates individuals with TBRS and their families, friends, and service providers.

• Public Foundations

• 467.

TNPO2 Foundation

TNPO2 FOUNDATION WORKED TO ACCELERATE ACCESS TO A CURE FOR ANY "N-OF-1" PATIENT.

• Public Foundations

• 468.

Dyspraxia Dcd America Inc

IlluminatingAwareness of DyspraxiaDCD Dyspraxia DCD America is a 501c3 nonprofit organization dedicated to raising awareness for this lifelong hidden disability.