• Nonmonetary Support N.E.C.*

• 595.

Kidz1Stfund Inc

Established by Coach Jimbo Fisher & Candi Fisher after their son was diagnosed with Fanconi anemia.

Saloni Heart Foundation

Every child with complex heart condition has access to the world's leading heart specialists @saloniheart @CHD Empower Parents of Patients with Special Hearts Every child with complex heart condition has access to the world's leading heart specialists A Journey of Hope Healing 1 frequently diagnosed congenital defect worldwide 1.

• Alliance/Advocacy Organizations

• 597.

Institute for Genetic Disease Prevention Inc

THE INSTITUTE FOR GENETIC DISEASE PREVENTION Our mission is to advance the cause of genetic disease prevention reducing the social economic and emotional burdens ofhighly morbid and lethal monogenic diseases within our lifetime.

• Alliance/Advocacy Organizations

• 598.

Marshalls Mountain Inc

Marshalls Mountain Pompe Disease Fundraising Marshalls Mountain was formed after our son was diagnosed with Pompe disease.

• Specifically Named Diseases Research

• 599.

INTERNATIONAL SOCIETY FOR MANNOSIDO

ISMRD is the leading advocate for families affected by a Glycoprotein Storage Disease.

• Nerve, Muscle, and Bone Diseases

• 600.

FUNDACION DE ESCLEROSIS MULTIPLE DE PUERTO RICO INC

La Fundación de Esclerosis Multiple de Puerto Rico está dirigida al bienestar de los pacientes que viven con esta condición en la Isla.

• Specifically Named Diseases Research

• 601.

MECP2 DUPLICATION FOUNDATION

The MECP2 Duplication Foundation is a family founded organization providing support to the MECP2 Duplication community.

WE ARE BLOOD

Every local patient treated at every hospital in our 10county service area relies exclusively on the generosity of We Are Blood platelet and blood donors.

• Birth Defects, Genetic Diseases

• 603.

THINKGENETIC FOUNDATION INC

Helping those living with a genetic disease by shortening the time to diagnose a genetic condition and providing actionable, patient-focused guidance.