• Alliance/Advocacy Organizations

• 145.

Lynch Syndrome International

MISSION STATEMENTThe primary mission of Lynch Syndrome International (LSI) is to serve our global communities by focusing on providing support for individuals afflicted with Lynch syndrome, creating public awareness of the syndrome, educating members of the general public and health care professionals and providing support for Lynch syndrome research endeavors.

• Lung

• 146.

Alpha 1 Association

Our mission is to increase awareness of and find a cure for Alpha-1 Antitrypsin Deficiency.

• Medical Specialty Research

• 147.

Foundation for the Study of Inflammatory Disease

Your Custom Text Here Inflammatory processes keep us alive.

• Birth Defects, Genetic Diseases Research

• 148.

Rory Belle Foundation

We are a family run foundation established to raise funding and awareness for a gene therapy cure for the NARS1 disease.

• Birth Defects, Genetic Diseases

• 149.

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.

• Fund Raising and/or Fund Distribution

• 150.

The Children's Rare Disorders Fund

Dedicated to curing rare genetic disorders Founded in July 2022 by parents of a toddler affected by FOXG1, The CRD Fund focuses on under served communities in the rare disorder space.

PACIFIC NORTHWEST RESEARCH INSTITUTE

PNRI unravels the powerful mysteries of genetics to drive future medical breakthroughs.

The Vision of Children Foundation

Dedicated to finding a cure for hereditary childhood blindness and vision disorders.

• Special Ed Institutions/ Schools for Visually or Hearing Impaired, Learning Disabled

• 153.

THE 21 CLUB OF CNY INC

Raising awareness supportingeducating and connectingpeople with Down syndrome and their families in the greater Utica andcentral New York area.